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Publications: Mastaglia, Frank

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Journal Article

Needham, M. and Mastaglia, F.L. (2017) Advances in inclusion body myositis: genetics, pathogenesis and clinical aspects. Expert Opinion on Orphan Drugs, 5 (5). pp. 431-443.

Evans, T., Jefferson, A., Byrnes, M., Walters, S., Ghosh, S., Mastaglia, F.L., Power, B. and Anderton, R.S. (2017) Extended “Timed Up and Go” assessment as a clinical indicator of cognitive state in Parkinson's disease. Journal of the Neurological Sciences, 375 . pp. 86-91.

Gutteridge, D.H. and Mastaglia, F.L. (2017) Recognition of giant cell arteritis in patients with polymyalgia rheumatica who have a stroke: A cautionary tale. Internal Medicine Journal, 47 (10). pp. 1199-1201.

Bundell, C., Rojana-udomsart, A., Mastaglia, F., Hollingsworth, P. and McLean-Tooke, A. (2016) Diagnostic performance of a commercial immunoblot assay for myositis antibody testing. Pathology, 48 (4). pp. 363-366.

Price, M.A., Barghout, V., Benveniste, O., Christopher-Stine, L., Corbett, A., de Visser, M., Hilton-Jones, D., Kissel, J.T., Lloyd, T.E., Lundberg, I.E., Mastaglia, F., Mozaffar, T., Needham, M., Schmidt, J., Sivakumar, K., DeMuro, C. and Tseng, B.S. (2016) Mortality and causes of death in patients with sporadic inclusion body myositis: Survey study based on the clinical experience of specialists in Australia, Europe and the USA. Journal of Neuromuscular Diseases, 3 (1). pp. 67-75.

Bates, K.A., Sohrabi, H.R., Rainey-Smith, S.R., Weinborn, M., Bucks, R.S., Rodrigues, M., Beilby, J., Howard, M., Taddei, K., Martins, G., Paton, A., Shah, T., Dhaliwal, S.S., Foster, J.K., Martins, I.J., Lautenschlager, N.T., Mastaglia, F.L., Gandy, S.E. and Martins, R.N. (2016) Serum high-density lipoprotein is associated with better cognitive function in a cross-sectional study of aging women. International Journal of Neuroscience, 127 (3). pp. 243-252.

Needham, M. and Mastaglia, F.L. (2016) Sporadic inclusion body myositis: A review of recent clinical advances and current approaches to diagnosis and treatment. Clinical Neurophysiology, 127 (5). pp. 1764-1773.

De Bleecker, J.L., De Paepe, B., Aronica, E., de Visser, M., Amato, A., Aronica, E., Benveniste, O., de Boer, O., Dimachkie, M., Gherardi, R., Goebel, H.H., Hilton-Jones, D., Holton, J., Lundberg, I.E., Mammen, A., Mastaglia, F., Nishino, I., Rushing, E., Daa Schroder, H., Selcen, D. and Stenzel, W. (2015) 205th ENMC International Workshop: Pathology diagnosis of idiopathic inflammatory myopathies Part II 28–30 March 2014, Naarden, The Netherlands. Neuromuscular Disorders, 25 (3). pp. 268-272.

Anderton, R.S. and Mastaglia, F.L. (2015) Advances and challenges in developing a therapy for spinal muscular atrophy. Expert Review of Neurotherapeutics, 15 (8). pp. 895-908.

Sohrabi, H.R., Bates, K.A., Weinborn, M., Bucks, R.S., Rainey-Smith, S.R., Rodrigues, M.A., Bird, S.M., Brown, B.M., Beilby, J., Howard, M., Criddle, A., Wraith, M., Taddei, K., Martins, G., Paton, A., Shah, T., Dhaliwal, S.S., Mehta, P.D., Foster, J.K., Martins, I.J., Lautenschlager, N.T., Mastaglia, F., Laws, S.M. and Martins, R.N. (2015) Bone mineral density, adiposity, and cognitive functions. Frontiers in Aging Neuroscience, 7 .

Limaye, V., Bundell, C., Hollingsworth, P., Rojana-udomsart, A., Mastaglia, F., Blumbergs, P. and Lester, S. (2015) Clinical and genetic associations of autoantibodies to 3-hydroxy-3-methyl-glutaryl-coenzyme a reductase in patients with immune-mediated myositis and necrotizing myopathy. Muscle & Nerve, 52 (2). pp. 196-203.

Luo, Y-B and Mastaglia, F.L. (2015) Dermatomyositis, polymyositis and immune-mediated necrotising myopathies. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1852 (4). pp. 622-632.

Silbert, B.I., Heaton, A.E., Cash, R.F.H., James, I., Dunne, J.W., Lawn, N.D., Silbert, P.L., Mastaglia, F.L. and Thickbroom, G.W. (2015) Evidence for an excitatory GABAA response in human motor cortex in idiopathic generalised epilepsy. Seizure, 26 . pp. 36-42.

Needham, M. and Mastaglia, F.L. (2015) Immunotherapies for Immune-Mediated myopathies: A current perspective. Neurotherapeutics, 13 (1). pp. 132-146.

Mastaglia, F.L. and Needham, M. (2015) Inclusion body myositis: A review of clinical and genetic aspects, diagnostic criteria and therapeutic approaches. Journal of Clinical Neuroscience, 22 (1). pp. 6-13.

Johnson, L., Rodrigues, J., Teo, W-P, Walters, S., Stell, R., Thickbroom, G. and Mastaglia, F. (2015) Interactive effects of GPI stimulation and levodopa on postural control in Parkinson's disease. Gait & Posture, 41 (4). pp. 929-934.

van der Stap, D.K.D., Rider, L.G., Alexanderson, H., Huber, A.M., Gualano, B., Gordon, P., van der Net, J., Mathiesen, P., Johnson, L.G., Ernste, F.C., Feldman, B.M., Houghton, K.M., Singh-Grewal, D., Kutzbach, A.G., Munters, L.A., Takken, T. and Mastaglia, F.L. (2015) Proposal for a candidate core set of fitness and strength tests for patients with childhood or adult idiopathic inflammatory myopathies. The Journal of Rheumatology, 43 (1). pp. 169-176.

Huang, Y., Wang, G., Rowe, D., Wang, Y., Kwok, J.B.J., Xiao, Q., Mastaglia, F., Liu, J., Chen, S-D and Halliday, G. (2015) SNCA Gene, but not MAPT, influences onset age of Parkinson’s Disease in Chinese and Australians. BioMed Research International, 2015 . pp. 1-6.

Gang, Q., Bettencourt, C., Machado, P.M., Fox, Z., Brady, S., Healy, E., Parton, M., Holton, J.L., Hilton-Jones, D., Shieh, P.B., Zanoteli, E., De Paepe, B., De Bleecker, J., Shaibani, A., Ripolone, M., Violano, R., Moggio, M., Barohn, R.J., Dimachkie, M.M., Mora, M., Mantegazza, R., Zanotti, S., Hanna, M.G., Houlden, H., Needham, M. and Mastaglia, F. (2015) The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis. Neurobiology of Aging, 36 (4). 1766.e1-1766.e3.

Luo, Y-B, Mitrpant, C., Adams, A.M., Johnsen, R.D., Fletcher, S., Mastaglia, F.L. and Wilton, S.D. (2014) Antisense oligonucleotide induction of progerin in human myogenic cells. PLoS ONE, 9 (6).

Moran, E.M. and Mastaglia, F.L. (2014) Cytokines in immune-mediated inflammatory myopathies: Cellular sources, multiple actions and therapeutic implications. Clinical & Experimental Immunology, 178 (3). pp. 405-415.

Rodríguez Cruz, P.M., Needham, M., Hollingsworth, P., Mastaglia, F.L. and Hillman, D.R (2014) G.P.65: Obstructive sleep apnoea and subclinical impairment of respiratory function are common in sporadic inclusion body myositis. Neuromuscular Disorders, 24 (9-10). p. 814.

Anderton, R., Meloni, B., Mastaglia, F. and Boulos, S. (2014) Investigation of a recombinant SMN protein delivery system to treat spinal muscular atrophy. Translational Neuroscience, 5 (1). pp. 8-16.

Kanyenda, L.J., Verdile, G., Martins, R., Meloni, B.P., Chieng, J., Mastaglia, F., Laws, S.M., Anderton, R.S. and Boulos, S. (2014) Is cholesterol and Amyloid-β stress induced CD147 expression a protective response? Evidence that extracellular cyclophilin a mediated neuroprotection is Reliant on CD147. Journal of Alzheimer's disease : JAD, 39 (3). pp. 545-556.

Teo, W-P, Rodrigues, J.P., Mastaglia, F.L. and Thickbroom, G.W. (2014) Modulation of corticomotor excitability after maximal or sustainable-rate repetitive finger movement is impaired in Parkinson’s disease and is reversed by levodopa. Clinical Neurophysiology, 125 (3). pp. 562-568.

Edwards, D.J., Dipietro, L., Demirtas-Tatlidede, A., Medeiros, A.H., Thickbroom, G.W., Mastaglia, F.L., Krebs, H.I. and Pascual-Leone, A. (2014) Movement-generated afference paired with transcranial magnetic stimulation: An associative stimulation paradigm. Journal of NeuroEngineering and Rehabilitation, 11 (1).

Luo, Y-B, Mastaglia, F.L. and Wilton, S.D. (2014) Normal and aberrant splicing of LMNA. Journal of Medical Genetics, 51 (4). pp. 215-223.

Rodríguez Cruz, P.M., Needham, M., Hollingsworth, P., Mastaglia, F.L. and Hillman, D.R. (2014) Sleep disordered breathing and subclinical impairment of respiratory function are common in sporadic inclusion body myositis. Neuromuscular Disorders, 24 (12). pp. 1036-1041.

Needham, M. and Mastaglia, F.L. (2014) Statin myotoxicity: A review of genetic susceptibility factors. Neuromuscular Disorders, 24 (1). pp. 4-15.

Rodríguez Cruz, P.M., Luo, Y-B, Miller, J., Junckerstorff, R.C., Mastaglia, F.L. and Fabian, V. (2014) An analysis of the sensitivity and specificity of MHC-I and MHC-II immunohistochemical staining in muscle biopsies for the diagnosis of inflammatory myopathies. Neuromuscular Disorders, 24 (12). pp. 1025-1035.

Moran, E.M. and Mastaglia, F.L. (2014) The role of interleukin-17 in immune-mediated inflammatory myopathies and possible therapeutic implications. Neuromuscular Disorders, 24 (11). pp. 943-952.

Rojana-udomsart, A., Mitrpant, C., James, I., Witt, C., Needham, M., Day, T., Kiers, L., Corbett, A., Martinez, P., Wilton, S.D. and Mastaglia, F.L. (2013) Analysis of HLA-DRB3 alleles and supertypical genotypes in the MHC Class II region in sporadic inclusion body myositis. Journal of Neuroimmunology, 254 (1-2). pp. 174-177.

Johnson, L., James, I., Rodrigues, J., Stell, R., Thickbroom, G. and Mastaglia, F. (2013) Clinical and posturographic correlates of falling in Parkinson's disease. Movement Disorders, 28 (9). pp. 1250-1256.

Teo, W.P., Rodrigues, J.P., Mastaglia, F.L. and Thickbroom, G.W. (2013) Comparing kinematic changes between a finger-tapping task and unconstrained finger flexion–extension task in patients with Parkinson’s disease. Experimental Brain Research, 227 (3). pp. 323-331.

Rojana-udomsart, A., Mitrpant, C., Bundell, C., Price, L., Luo, Y-B, Fabian, V., Wilton, S.D., Hollingsworth, P. and Mastaglia, F.L. (2013) Complement-mediated muscle cell lysis: A possible mechanism of myonecrosis in anti-SRP associated necrotizing myopathy (ASANM). Journal of Neuroimmunology, 264 (1-2). pp. 65-70.

Cash, R.F.H., Mastaglia, F.L. and Thickbroom, G. W. (2013) Evidence for high-fidelity timing-dependent synaptic plasticity of human motor cortex. Journal of Neurophysiology, 109 (1). pp. 106-112.

Greene, I.D., Mastaglia, F., Meloni, B.P., West, K.A., Chieng, J., Mitchell, C.J., Gai, W-P and Boulos, S. (2013) Evidence that the LRRK2 ROC domain Parkinson's disease-associated mutants A1442P and R1441C exhibit increased intracellular degradation. Journal of Neuroscience Research, 92 (4). pp. 506-516.

Luo, Y-B, Mitrpant, C., Johnsen, R.D., Fabian, V.A., Fletcher, S., Mastaglia, F.L. and Wilton, S.D. (2013) Investigation of age-related changes in LMNA splicing and expression of progerin in human skeletal muscles. International Journal of Clinical and Experimental Pathology, 6 (12). pp. 2778-2786.

Luo, Y-B, Mitrpant, C., Johnsen, R., Fabian, V., Needham, M., Fletcher, S., Wilton, S.D. and Mastaglia, F.L. (2013) Investigation of splicing changes and post-translational processing of LMNA in sporadic inclusion body myositis. International Journal of Clinical and Experimental Pathology, 6 (9). pp. 1723-1733.

Mastaglia, F.L., Rojana-udomsart, A., James, I., Needham, M., Day, T.J., Kiers, L., Corbett, J.A., Saunders, A.M., Lutz, M.W. and Roses, A.D. (2013) Polymorphism in the TOMM40 gene modifies the risk of developing sporadic inclusion body myositis and the age of onset of symptoms. Neuromuscular Disorders, 23 (12). pp. 969-974.

Luo, Y-B, Johnsen, R.D., Griffiths, L., Needham, M., Fabian, V.A., Fletcher, S., Wilton, S.D. and Mastaglia, F.L. (2013) Primary over-expression of AβPP in muscle does not lead to the development of inclusion body myositis in a new lineage of the MCK-AβPP transgenic mouse. International Journal of Experimental Pathology, 94 (6). pp. 418-425.

Anderton, R.S., Meloni, B.P., Mastaglia, F.L. and Boulos, S. (2013) Spinal muscular atrophy and the Antiapoptotic role of Survival of Motor Neuron (SMN) protein. Molecular Neurobiology, 47 (2). pp. 821-832.

Johnson, L., Putrino, D., James, I., Rodrigues, J., Stell, R., Thickbroom, G. and Mastaglia, F.L. (2013) The effects of a supervised Pilates training program on balance in Parkinson’s disease. Advances in Parkinson's Disease, 02 (02). pp. 58-61.

Qiu, W., Pham, K., James, I., Nolan, D., Castley, A., Christiansen, F.T., Czarniak, P., Luo, Y., Wu, J., Garlepp, M., Wilton, S., Carroll, W.M., Mastaglia, F.L. and Kermode, A.G. (2013) The influence of non-HLA gene polymorphisms and interactions on disease risk in a Western Australian multiple sclerosis cohort. Journal of Neuroimmunology, 261 (1-2). pp. 92-97.

Teo, W.P., Rodrigues, J.P., Mastaglia, F.L. and Thickbroom, G.W. (2012) Breakdown in central motor control can be attenuated by motor practice and neuro-modulation of the primary motor cortex. Neuroscience, 220 . pp. 11-18.

Teo, W.P., Rodrigues, J.P., Mastaglia, F.L. and Thickbroom, G.W. (2012) Changes in corticomotor excitability and inhibition after exercise are influenced by hand dominance and motor demand. Neuroscience, 210 . pp. 110-117.

Anderton, R.S., Price, L.L., Turner, B.J., Meloni, B.P., Mitrpant, C., Mastaglia, F.L., Goh, C., Wilton, S.D. and Boulos, S. (2012) Co-regulation of survival of motor neuron and Bcl-xL expression: Implications for neuroprotection in spinal muscular atrophy. Neuroscience, 220 . pp. 228-236.

Nolan, D., Castley, A., Tschochner, M., James, I., Qiu, W., Sayer, D., Christiansen, F.T., Witt, C., Mastaglia, F., Carroll, W. and Kermode, A. (2012) Contributions of vitamin D response elements and HLA promoters to multiple sclerosis risk. Neurology, 79 (6). pp. 538-546.

Mulcahy, K.P., Langdon, P.C. and Mastaglia, F. (2012) Dysphagia in inflammatory myopathy: Self-report, incidence, and prevalence. Dysphagia, 27 (1). pp. 64-69.

Rojana-udomsart, A., Bundell, C., James, I., Castley, A., Martinez, P., Christiansen, F., Hollingsworth, P. and Mastaglia, F. (2012) Frequency of autoantibodies and correlation with HLA-DRB1 genotype in sporadic inclusion body myositis (s-IBM): A population control study. Journal of Neuroimmunology, 249 (1-2). pp. 66-70.

Lau, S., Bates, K.A., Sohrabi, H.R., Rodrigues, M., Martins, G., Dhaliwal, S.S., Taddei, K., Laws, S.M., Martins, I.., Mastaglia, F.L., Foster, J.K., Phillips, J.K. and Martins, R.N. (2012) Functional effects of genetic polymorphism in inflammatory genes in subjective memory complainers. Neurobiology of Aging, 33 (6). pp. 1054-1056.

Rojana-udomsart, A., Castley, A., James, I., Needham, M., Scott, A., Day, T., Kiers, L., Corbett, A., Sue, C., Martinez, P., Christiansen, F. and Mastaglia, F.L. (2012) G.P.63 High-resolution analysis of HLA-DRB1 alleles and diplotypes in an Australian inclusion body myositis cohort. Neuromuscular Disorders, 22 (9-10). pp. 853-854.

Rojana-udomsart, A., James, I., Castley, A., Needham, M., Scott, A., Day, T., Kiers, L., Corbett, A., Sue, C., Witt, C., Martinez, P., Christiansen, F. and Mastaglia, F. (2012) High-resolution HLA-DRB1 genotyping in an Australian inclusion body myositis (s-IBM) cohort: An analysis of disease-associated alleles and diplotypes. Journal of Neuroimmunology, 250 (1-2). pp. 77-82.

Scott, A.P., Laing, N.G., Mastaglia, F., Dalakas, M., Needham, M. and Allcock, R.J.N. (2012) Investigation of NOTCH4 coding region polymorphisms in sporadic inclusion body myositis. Journal of Neuroimmunology, 250 (1-2). pp. 66-70.

Langdon, P.C., Mulcahy, K., Shepherd, K.L., Low, V.H. and Mastaglia, F.L. (2012) Pharyngeal dysphagia in inflammatory muscle diseases resulting from Iimpaired suprahyoid musculature. Dysphagia, 27 (3). pp. 408-417.

Teo, W.P., Rodrigues, J.P., Mastaglia, F.L. and Thickbroom, G.W. (2012) Post-exercise depression in corticomotor excitability after dynamic movement: A general property of fatiguing and non-fatiguing exercise. Experimental Brain Research, 216 (1). pp. 41-49.

Mastaglia, F.L. and Needham, M. (2012) Update on toxic myopathies. Current Neurology and Neuroscience Reports, 12 (1). pp. 54-61.

Mastaglia, F.L. (2012) The relationship between muscle pain and fatigue. Neuromuscular Disorders, 22 (Supp. 3). S178-S180.

Sambuughin, N., Yau, K.S., Olivé, M., Duff, R.M., Bayarsaikhan, M., Lu, S., Gonzalez-Mera, L., Sivadorai, P., Nowak, K.J., Ravenscroft, G., Mastaglia, F.L., North, K.N., Ilkovski, B., Kremer, H., Lammens, M., van Engelen, B.G.M., Fabian, V., Lamont, P., Davis, M.R., Laing, N.G. and Goldfarb, L.G. (2011) Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores. The American Journal of Human Genetics, 88 (1). p. 122.

Qiu, W., James, I., Carroll, W.M., Mastaglia, F.L. and Kermode, A.G. (2011) HLA-DR allele polymorphism and multiple sclerosis in Chinese populations: a meta-analysis. Multiple Sclerosis, 17 (4). pp. 382-388.

Qiu, W., Raven, S., Wu, J-S, Bundell, C., Hollingsworth, P., Carroll, W.M., Mastaglia, F.L. and Kermode, A.G. (2011) Hypothalamic lesions in multiple sclerosis. Journal of Neurology, Neurosurgery & Psychiatry, 82 (7). pp. 819-822.

Silbert, B.I., Gibbons, J.T., Cash, R.H.F., Mastaglia, F.L. and Thickbroom, G.W. (2011) Modulation of corticomotor excitability by an I-wave intervention delivered during low-level voluntary contraction. Experimental Brain Research, 208 (2). pp. 229-235.

Scott, A.P., Laing, N.G., Mastaglia, F., Needham, M., Walter, M.C., Dalakas, M.C. and Allcock, R.J.N. (2011) Recombination mapping of the susceptibility region for sporadic inclusion body myositis within the major histocompatibility complex. Journal of Neuroimmunology, 235 (1-2). pp. 77-83.

Qiu, W., Raven, S., James, I., Luo, Y., Wu, J., Castley, A., Christiansen, F.T., Carroll, W.M., Mastaglia, F.L. and Kermode, A.G. (2011) Spinal cord involvement in multiple sclerosis: A correlative MRI and high-resolution HLA-DRB1 genotyping study. Journal of the Neurological Sciences, 300 (1-2). pp. 114-119.

Anderton, R.S., Meloni, B.P., Mastaglia, F.L., Greene, W.K. and Boulos, S. (2011) Survival of motor neuron protein over-expression prevents calpain-mediated cleavage and activation of procaspase-3 in differentiated human SH-SY5Y cells. Neuroscience, 181 . pp. 226-233.

Rojana-udomsart, A., Needham, M., Luo, Y.B., Fabian, V., Walters, S., Zilko, P.J. and Mastaglia, F.L. (2011) The association of sporadic inclusion body myositis and Sjögren's syndrome in carriers of HLA-DR3 and the 8.1 MHC ancestral haplotype. Clinical Neurology and Neurosurgery, 113 (7). pp. 559-563.

Kanyenda, L.J., Verdile, G., Boulos, S., Krishnaswamy, S., Taddei, K., Meloni, B.P., Mastaglia, F.L. and Martins, R.N. (2011) The dynamics of CD147 in Alzheimer's disease development and pathology. Journal of Alzheimer's disease : JAD, 26 (4). pp. 593-605.

Meade, A.J., Meloni, B.P., Cross, J., Bakker, A.J., Fear, M.W., Mastaglia, F.L., Watt, P.M. and Knuckey, N.W. (2010) AP-1 inhibitory peptides are neuroprotective following acute glutamate excitotoxicity in primary cortical neuronal cultures. Journal of Neurochemistry, 112 (1). pp. 258-270.

Meade, A.J., Meloni, B.P., Mastaglia, F.L., Watt, P.M. and Knuckey, N.W. (2010) AP-1 inhibitory peptides attenuate in vitro cortical neuronal cell death induced by kainic acid. Brain Research, 1360 . pp. 8-16.

Qiu, W., Wu, J-S, Castley, A., James, I., Joseph, J., Christiansen, F.T., Carroll, W.M., Mastaglia, F.L. and Kermode, A.G. (2010) Clinical profile and HLA-DRB1 genotype of late onset multiple sclerosis in Western Australia. Journal of Clinical Neuroscience, 17 (8). pp. 1009-1013.

Putrino, D., Brown, E.N., Mastaglia, F.L. and Ghosh, S. (2010) Differential involvement of excitatory and inhibitory neurons of Cat Motor Cortex in coincident spike activity related to behavioral context. Journal of Neuroscience, 30 (23). pp. 8048-8056.

Sambuughin, N., Yau, K.S., Olivé, M., Duff, R.M., Bayarsaikhan, M., Lu, S., Gonzalez-Mera, L., Sivadorai, P., Nowak, K.J., Ravenscroft, G., Mastaglia, F.L., North, K.N., Ilkovski, B., Kremer, H., Lammens, M., van Engelen, B.G.M., Fabian, V., Lamont, P., Davis, M.R., Laing, N.G. and Goldfarb, L.G. (2010) Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores. The American Journal of Human Genetics, 87 (6). pp. 842-847.

Wu, J-S, James, I., Qiu, W., Castley, A., Christiansen, F.T., Carroll, W.M., Mastaglia, F.L. and Kermode, A.G. (2010) HLA-DRB1 allele heterogeneity influences multiple sclerosis severity as well as risk in Western Australia. Journal of Neuroimmunology, 219 (1-2). pp. 109-113.

Mastaglia, F.L. (2010) Iatrogenic myopathies. Current Opinion in Neurology, 23 (5). pp. 445-449.

Wu, J.S., James, I., Wei, Q., Castley, A., Christiansen, F.T., Carroll, W.M., Mastaglia, F.L. and Kermode, A.G. (2010) Influence of HLA-DRB1 allele heterogeneity on disease risk and clinical course in a West Australian MS cohort: a high-resolution genotyping study. Multiple Sclerosis, 16 (5). pp. 526-532.

Qiu, W., Wu, J-S, Zhang, M-N, Matsushita, T., Kira, J-I, Carroll, W.M., Mastaglia, F.L. and Kermode, A.G. (2010) Longitudinally extensive myelopathy in caucasians: A West Australian study of 26 cases from the Perth Demyelinating Diseases Database. Journal of Neurology, Neurosurgery & Psychiatry, 81 (2). pp. 209-212.

Qiu, W., Bundell, C., Wu, J.-S., Castley, A., James, I., Hollingsworth, P., Christiansen, F., Carroll, W.M., Mastaglia, F.L. and Kermode, A.G. (2010) Low level of systemic autoimmunity in Western Australian multiple sclerosis patients. Multiple Sclerosis, 16 (3). pp. 351-354.

Wu, J-S, Qiu, W., Castley, A., James, I., Mastaglia, F.L., Christiansen, F.T, Carroll, W.M, Joseph, J. and Kermode, A.G. (2010) Modifying effects of HLA-DRB1 allele interactions on age at onset of multiple sclerosis in Western Australia. Multiple Sclerosis, 16 (1). pp. 15-20.

Putrino, D., Mastaglia, F.L. and Ghosh, S. (2010) Neural integration of reaching and posture: Interhemispheric spike correlations in cat motor cortex. Experimental Brain Research, 202 (4). pp. 765-777.

Rojana-udomsart, A., Fabian, V., Hollingsworth, P.N., Walters, S.E., Zilko, P.J. and Mastaglia, F.L. (2010) Paraspinal and scapular myopathy associated with scleroderma. Journal of Clinical Neuromuscular Disease, 11 (4). pp. 213-222.

Wu, J-S, Qiu, W., Castley, A., James, I., Joseph, J., Christiansen, F.T., Carroll, W.M., Mastaglia, F.L. and Kermode, A.G. (2010) Presence of CSF oligoclonal bands (OCB) is associated with the HLA-DRB1 genotype in a West Australian multiple sclerosis cohort. Journal of the Neurological Sciences, 288 (1-2). pp. 63-67.

Kumar, K.R., Needham, M., Mina, K., Davis, M., Brewer, J., Staples, C., Ng, K., Sue, C.M. and Mastaglia, F.L. (2010) Two Australian families with inclusion-body myopathy, Paget’s disease of bone and frontotemporal dementia: Novel clinical and genetic findings. Neuromuscular Disorders, 20 (5). pp. 330-334.

Qiu, W., Raven, S., Wu, J-S, Carroll, W.M., Mastaglia, F.L. and Kermode, A.G. (2010) Wedge-shaped medullary lesions in multiple sclerosis. Journal of the Neurological Sciences, 290 (1-2). pp. 190-193.

Bates, K.A., Sohrabi, H.R., Rodrigues, M., Beilby, J., Dhaliwal, S.S., Taddei, K., Criddle, A., Wraith, M., Howard, M., Martins, G., Paton, A., Mehta, P., Foster, J.K., Martins, I.J., Lautenschlager, N.T., Mastaglia, F.L., Laws, S.M., Gandy, S.E. and Martins, R.N. (2009) Association of cardiovascular factors and Alzheimer's disease plasma Amyloid-β protein in subjective memory complainers. Journal of Alzheimer's Disease, 17 (2). pp. 305-318.

Sutherland, G.T., Halliday, G.M., Silburn, P.A., Mastaglia, F.L., Rowe, D.B., Boyle, R.S., O'Sullivan, J.D., Ly, T., Wilton, S.D. and Mellick, G.D. (2009) Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease? Movement Disorders, 24 (6). pp. 833-838.

Mastaglia, F.L., Needham, M., Scott, A., James, I., Day, T., Kiers, L., Corbett, A., Witt, C., Garlepp, M., Allcock, R., Laing, N. and Christiansen, F. (2009) G.P.16.09 Epistatic interactions between DRB1 alleles influence susceptibility and clinical phenotype in sporadic inclusion body myositis (sIBM). Neuromuscular Disorders, 19 (8-9). p. 654.

Johnson, L.G., Collier, K.E., Edwards, D.J., Philippe, D.L., Eastwood, P.R., Walters, S.E., Thickbroom, G.W. and Mastaglia, F.L. (2009) Improvement in aerobic capacity after an exercise program in sporadic inclusion body myositis. Journal of Clinical Neuromuscular Disease, 10 (4). pp. 178-184.

Cash, R.F.H., Benwell, N.M., Murray, K., Mastaglia, F.L. and Thickbroom, G.W. (2009) Neuromodulation by paired-pulse TMS at an I-wave interval facilitates multiple I-waves. Experimental Brain Research, 193 (1). pp. 1-7.

Thickbroom, G.W. and Mastaglia, F.L. (2009) Plasticity in neurological disorders and challenges for noninvasive brain stimulation (NBS). Journal of NeuroEngineering and Rehabilitation, 6 (1).

Edwards, D.J., Krebs, H.I., Rykman, A., Zipse, J., Thickbroom, G.W., Mastaglia, F.L., Pascual-Leone, A. and Volpe, B.T. (2009) Raised corticomotor excitability of M1 forearm area following anodal tDCS is sustained during robotic wrist therapy in chronic stroke. Restorative Neurology and Neuroscience, 27 (3). pp. 199-207.

Rodrigues, J.P., Mastaglia, F.L. and Thickbroom, G.W. (2009) Rapid slowing of maximal finger movement rate: Fatigue of central motor control? Experimental Brain Research, 196 (4). pp. 557-563.

Mastaglia, F. (2009) Sporadic inclusion body myositis: Evidence of a link between inflammation, cell stress and β-amyloid deposition. Journal of Neurology, Neurosurgery & Psychiatry, 80 (12). p. 1301.

Mastaglia, F.L., Needham, M., Scott, A., James, I., Zilko, P., Day, T., Kiers, L., Corbett, A., Witt, C.S., Allcock, R., Laing, N., Garlepp, M. and Christiansen, F.T. (2009) Sporadic inclusion body myositis: HLA-DRB1 allele interactions influence disease risk and clinical phenotype. Neuromuscular Disorders, 19 (11). pp. 763-765.

Mastaglia, F.L. (2009) Sporadic inclusion body myositis: Variability in prevalence and phenotype and influence of the MHC. Acta Myologica : Myopathies and cardiomyopathies : Official journal of the Mediterranean Society of Myology, 28 (2). pp. 66-71.

Qiu, W., Wu, J-S, Carroll, W.M., Mastaglia, F.L. and Kermode, A.G. (2009) Wallenberg syndrome caused by multiple sclerosis mimicking stroke. Journal of Clinical Neuroscience, 16 (12). pp. 1700-1702.

Needham, M., Hooper, A., James, I., van Bockxmeer, F., Corbett, A., Day, T., Garlepp, M.J. and Mastaglia, F.L. (2008) Apolipoprotein ε alleles in sporadic inclusion body myositis: A reappraisal. Neuromuscular Disorders, 18 (2). pp. 150-152.

Thickbroom, G.W., Sacco, P., Faulkner, D.L., Kermode, A.G. and Mastaglia, F.L. (2008) Enhanced corticomotor excitability with dynamic fatiguing exercise of the lower limb in multiple sclerosis. Journal of Neurology, 255 (7). pp. 1001-1005.

Needham, M., Scott, A., Christiansen, F., James, I., Corbett, A., Day, T., Kiers, L., Laing, N., Allcock, R. and Mastaglia, F.L. (2008) G.P.5.06 HLA alleles and MHC haplotypes in sporadic inclusion body myositis: Frequencies and phenotypic correlations. Neuromuscular Disorders, 18 (9-10). pp. 770-771.

Garlepp, M.J. and Mastaglia, F.L. (2008) Inclusion body myositis: New insights into pathogenesis. Current Opinion in Rheumatology, 20 (6). pp. 662-668.

Mastaglia, F.L. (2008) Inflammatory muscle diseases. Neurology India, 56 (3). p. 263.

Mechler, F., Mastaglia, F.L., Serena, M., Jenkison, M., Johnson, M.A., Fawcett, P.R.W., Hudgson, P. and Walton, J.N. (2008) Mitochondrial myopathies. A clinico-pathological study of cases with and without extra-ocular muscle involvement. Australian and New Zealand Journal of Medicine, 16 (2). pp. 185-192.

Needham, M., Corbett, A., Day, T., Christiansen, F., Fabian, V. and Mastaglia, F.L. (2008) Prevalence of sporadic inclusion body myositis and factors contributing to delayed diagnosis. Journal of Clinical Neuroscience, 15 (12). pp. 1350-1353.

Rodrigues, J.P., Walters, S.E., Stell, R., Mastaglia, F.L. and Thickbroom, G.W. (2008) Spike-timing-related plasticity is preserved in Parkinson's disease and is enhanced by dopamine: Evidence from transcranial magnetic stimulatio. Neuroscience Letters, 448 (1). pp. 29-32.

Needham, M. and Mastaglia, F.L. (2008) Sporadic inclusion body myositis: A continuing puzzle. Neuromuscular Disorders, 18 (1). pp. 6-16.

Needham, M., James, I., Corbett, A., Day, T., Christiansen, F., Phillips, B. and Mastaglia, F.L. (2008) Sporadic inclusion body myositis: Phenotypic variability and influence of HLA-DR3 in a cohort of 57 Australian cases. Journal of Neurology, Neurosurgery & Psychiatry, 79 (9). pp. 1056-1060.

Edwards, D.J., Mastaglia, F.L., Byrnes, M.L., Fregni, F., Pascual-Leone, A. and Thickbroom, G.W. (2008) Supraspinal inputs reduce corticomotor excitability during passive movement: Evidence from a pure sensory stroke. Restorative Neurology and Neuroscience, 25 (5-6). pp. 527-533.

Mastaglia, F.L. (2008) What to do ... When the treatment does not work: Polymyositis. Postgraduate Medical Journal, 84 (993). pp. 382-384.

Needham, M., Fabian, V., Knezevic, W., Lamont, P., Panegyres, P., Zilko, P. and Mastaglia, F. (2007) 632: Statins may initiate a persisting immune-mediated myopathy and myositis: A study of 10 cases. Journal of Clinical Neuroscience, 14 (10). p. 1029.

Benwell, N.M., Mastaglia, F.L. and Thickbroom, G.W. (2007) Changes in the functional MR signal in motor and non-motor areas during intermittent fatiguing hand exercise. Experimental Brain Research, 182 (1). pp. 93-97.

Benwell, N.M., Mastaglia, F.L. and Thickbroom, G.W. (2007) Differential changes in long-interval intracortical inhibition and silent period duration during fatiguing hand exercise. Experimental Brain Research, 179 (2). pp. 255-262.

Needham, M., Corbett, A., Day, T. and Mastaglia, F. (2007) G.P.13.06 Sporadic inclusion body myositis (sIBM): A phenotypic spectrum in a cohort of 57 cases. Neuromuscular Disorders, 17 (9-10). p. 850.

Needham, M., Corbett, A., Day, T., Fabian, V. and Mastaglia, F. (2007) G.P.13.07 Prevalence and diagnosis of sporadic inclusion body myositis (sIBM) in Western Australia. Neuromuscular Disorders, 17 (9-10). pp. 850-851.

Scott, A., Laing, N., Mastaglia, F., Needham, M., Walter, M., Dalakas, M. and Allcock, R. (2007) G.P.13.17 Recombinant mapping of MHC susceptibility region in sporadic inclusion body myositis (sIBM). Neuromuscular Disorders, 17 (9-10). pp. 853-854.

Needham, M., Mastaglia, F.L. and Garlepp, M.J. (2007) Genetics of inclusion-body myositis. Muscle & Nerve, 35 (5). pp. 549-561.

Rodrigues, J.P., Walters, S.E., Watson, P., Stell, R. and Mastaglia, F.L. (2007) Globus pallidus stimulation improves both motor and nonmotor aspects of quality of life in advanced Parkinson's disease. Movement Disorders, 22 (13). pp. 1866-1870.

Rodrigues, J.P., Walters, S.E., Watson, P., Stell, R. and Mastaglia, F.L. (2007) Globus pallidus stimulation in advanced Parkinson’s disease. Journal of Clinical Neuroscience, 14 (3). pp. 208-215.

Needham, M. and Mastaglia, F.L. (2007) Inclusion body myositis: Current pathogenetic concepts and diagnostic and therapeutic approaches. The Lancet Neurology, 6 (7). pp. 620-631.

Dundas, J.E., Thickbroom, G.W. and Mastaglia, F.L. (2007) Perception of comfort during transcranial DC stimulation: Effect of NaCl solution concentration applied to sponge electrodes. Clinical Neurophysiology, 118 (5). pp. 1166-1170.

Huang, Y., Halliday, G.M., Vandebona, H., Mellick, G.D., Mastaglia, F., Stevens, J., Kwok, J., Garlepp, M., Silburn, P.A., Horne, M.K., Kotschet, K., Venn, A., Rowe, D.B., Rubio, J.P. and Sue, C.M. (2007) Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's Disease. Movement Disorders, 22 (7). pp. 982-989.

Needham, M., Fabian, V., Knezevicˇ, W., Panegyres, P., Zilko, P. and Mastaglia, F.L. (2007) Progressive myopathy with up-regulation of MHC-I associated with statin therapy. Neuromuscular Disorders, 17 (2). pp. 194-200.

Mastaglia, F.L. and Argov, Z. (2007) Toxic and iatrogenic myopathies. Handbook of Clinical Neurology, 86 . pp. 321-341.

Johnson, L.G., Edwards, D.J., Walters, S., Thickbroom, G.W. and Mastaglia, F.L. (2007) The effectiveness of an individualized, Home-Based functional exercise program for patients with sporadic inclusion body myositis. Journal of Clinical Neuromuscular Disease, 8 (4). pp. 187-194.

Rodrigues, J.P., Edwards, D.J., Walters, S.E., Byrnes, M.L., Thickbroom, G.W., Stell, R. and Mastaglia, F.L. (2006) Blinded placebo crossover study of gabapentin in primary orthostatic tremor. Movement Disorders, 21 (7). pp. 900-905.

Thickbroom, G.W., Sacco, P., Kermode, A.G., Archer, S.A., Byrnes, M.L., Guilfoyle, A. and Mastaglia, F.L. (2006) Central motor drive and perception of effort during fatigue in multiple sclerosis. Journal of Neurology, 253 (8). pp. 1048-1053.

Blacker, D., Byrnes, M.L., Mastaglia, F.L. and Thickbroom, G.W. (2006) Differential activation of frontal lobe areas by lexical and semantic language tasks: A functional magnetic resonance imaging study. Journal of Clinical Neuroscience, 13 (1). pp. 91-95.

Mastaglia, F.L. (2006) Drug induced myopathies. Practical Neurology, 6 (1). pp. 4-13.

Mastaglia, F., Price, P., Walters, S., Fabian, V., Miller, J. and Zilko, P. (2006) Familial inclusion body myositis in a mother and son with different ancestral MHC haplotypes. Neuromuscular Disorders, 16 (11). pp. 754-758.

Lamont, P.J., Udd, B., Mastaglia, F.L., de Visser, M., Hedera, P., Voit, T., Bridges, L.R., Fabian, V., Rozemuller, A. and Laing, N.G. (2006) Laing early onset distal myopathy: Slow myosin defect with variable abnormalities on muscle biopsy. Journal of Neurology, Neurosurgery & Psychiatry, 77 (2). pp. 208-215.

Benwell, N.M., Mastaglia, F.L. and Thickbroom, G.W. (2006) Paired-pulse rTMS at trans-synaptic intervals increases corticomotor excitability and reduces the rate of force loss during a fatiguing exercise of the hand. Experimental Brain Research, 175 (4). pp. 626-632.

Benwell, N.M., Mastaglia, F.L. and Thickbroom, G.W. (2006) Reduced functional activation after fatiguing exercise is not confined to primary motor areas. Experimental Brain Research, 175 (4). pp. 575-583.

Thickbroom, G., Byrnes, M., Edwards, D. and Mastaglia, F. (2006) Repetitive paired-pulse TMS at I-wave periodicity markedly increases corticospinal excitability: A new technique for modulating synaptic plasticity. Clinical Neurophysiology, 117 (1). pp. 61-66.

Benwell, N.M., Sacco, P., Hammond, G.R., Byrnes, M.L., Mastaglia, F.L. and Thickbroom, G.W. (2006) Short-interval cortical inhibition and corticomotor excitability with fatiguing hand exercise: A central adaptation to fatigue? Experimental Brain Research, 170 (2). pp. 191-198.

Scott, A.P., Allcock, R.J.N., Mastaglia, F., Nishino, I., Nonaka, I. and Laing, N. (2006) Sporadic inclusion body myositis in Japanese is associated with the MHC ancestral haplotype 52.1. Neuromuscular Disorders, 16 (5). pp. 311-315.

Thickbroom, G.W., Byrnes, M.L., Archer, S.A., Kermode, A.G. and Mastaglia, F.L. (2005) Corticomotor organisation and motor function in multiple sclerosis. Journal of Neurology, 252 (7). pp. 765-771.

Mastaglia, F.L., Lamont, P.J. and Laing, N.G. (2005) Distal myopathies. Current Opinion in Neurology, 18 (5). pp. 504-510.

Rodrigues, J.P., Edwards, D.J., Walters, S.E., Byrnes, M.L., Thickbroom, G., Stell, R. and Mastaglia, F.L. (2005) Gabapentin can improve postural stability and quality of life in primary orthostatic tremor. Movement Disorders, 20 (7). pp. 865-870.

Mastaglia, F.L. (2005) Neuromuscular disorders: Molecular and therapeutic insights. The Lancet Neurology, 4 (1). pp. 6-7.

Haynes, M.J., Cala, L.A., Melsom, A., Mastaglia, F.L., Milne, N. and McGeachie, J.K. (2005) Posterior ponticles and rotational stenosis of vertebral arteries. A pilot study using Doppler ultrasound velocimetry and magnetic resonance angiography. Journal of Manipulative and Physiological Therapeutics, 28 (5). pp. 323-329.

Benwell, N.M., Byrnes, M.L., Mastaglia, F.L. and Thickbroom, G.W. (2005) Primary sensorimotor cortex activation with task-performance after fatiguing hand exercise. Experimental Brain Research, 167 (2). pp. 160-164.

Byrnes, M.L., Mastaglia, F.L., Walters, S.E., Archer, S-A.R. and Thickbroom, G.W. (2005) Primary writing tremor: Motor cortex reorganisation and disinhibition. Journal of Clinical Neuroscience, 12 (1). pp. 102-104.

Li, Y.J., Hauser, M.A., Scott, W.K., Martin, E.R., Booze, M.W., Qin, X.J., Walter, J.W., Nance, M.A., Hubble, J.P., Koller, W.C., Pahwa, R., Stern, M.B., Hiner, B.C., Jankovic, J., Goetz, C.G., Small, G.W., Mastaglia, F., Haines, J.L., Pericak-Vance, M.A. and Vance, J.M. (2004) Apolipoprotein E controls the risk and age at onset of Parkinson disease. Neurology, 62 (11). pp. 2005-2009.

Thickbroom, G.W., Byrnes, M.L., Morris, I.T., Fallon, M.J., Knuckey, N.W. and Mastaglia, F.L. (2004) Functional MRI near vascular anomalies: Comparison of cavernoma and arteriovenous malformation. Journal of Clinical Neuroscience, 11 (8). pp. 845-848.

Li, Y-J, Oliveira, S.A., Puting, X., Martin, E.R., Stenger, J.E., Hulette, C., Scherzer, C.R., Hauser, M.A., Scott, W.K., Small, G.W., Nance, M.A., Watts, R.L., Hubble, J.P., Koller, W.C., Pahwa, R., Stern, M.B., Hiner, B.C., Jankovic, J., Goetz, C.G., Mastaglia, F., Middleton, L.T., Roses, A.D., Saunders, A.M., Welsh-Bohmer, K.A., Schmechel, D.E., Gullans, S.R., Haines, J.L., Gilbert, J.R., Vance, J.M. and Pericak-Vance, M.A. (2004) Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease. Human Molecular Genetics, 13 (5). p. 573.

Thickbroom, G.W., Byrnes, M.L., Archer, S.A. and Mastaglia, F.L. (2004) Motor outcome after subcortical stroke correlates with the degree of cortical reorganization. Clinical Neurophysiology, 115 (9). pp. 2144-2150.

Meredith, C., Herrmann, R., Parry, C., Liyanage, K., Dye, D.E., Durling, H.J., Duff, R.M., Beckman, K., de Visser, M., van der Graaff, M.M., Hedera, P., Fink, J.K., Petty, E.M., Lamont, P., Fabian, V., Bridges, L., Voit, T., Mastaglia, F.L. and Laing, N.G. (2004) Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause Laing Early-Onset distal myopathy (MPD1). The American Journal of Human Genetics, 75 (4). pp. 703-708.

Edwards, D.J., Thickbroom, G.W., Byrnes, M.L., Ghosh, S. and Mastaglia, F.L. (2004) Temporal aspects of passive movement-related corticomotor inhibition. Human Movement Science, 23 (3-4). pp. 379-387.

Hammond, G., Faulkner, D., Byrnes, M., Mastaglia, F. and Thickbroom, G. (2004) Transcranial magnetic stimulation reveals asymmetrical efficacy of intracortical circuits in primary motor cortex. Experimental Brain Research, 155 (1). pp. 19-23.

Price, P., Santoso, L., Mastaglia, F., Garlepp, M., Kok, C.C., Allcock, R. and Laing, N. (2004) Two major histocompatibility complex haplotypes influence susceptibility to sporadic inclusion body myositis: Critical evaluation of an association with HLA-DR3. Tissue Antigens, 64 (5). pp. 575-580.

Lamont, P.J., Jacob, R., Mastaglia, F. and Laing, N. (2004) An expansion in the ZNF9 gene causes PROMM in a previously described family with an incidental CLCN1 mutation. Journal of Neurology, Neurosurgery & Psychiatry, 75 (2). p. 343.

Oliveira, S.A., Scott, W.K., Nance, M.A., Watts, R.L., Hubble, J.P., Koller, W.C., Lyons, K.E., Pahwa, R., Stern, M.B., Hiner, B.C., Jankovic, J., Ondo, W.G., Allen, Jr, F.H., Scott, B.L., Goetz, C.G., Small, G.W., Mastaglia, F.L., Stajich, J.M., Zhang, F., Booze, M.W., Reaves, J.A., Middleton, L.T., Haines, J.L., Pericak-Vance, M.A., Vance, J.M. and Martin, E.R. (2003) Association study of parkin gene polymorphisms with idiopathic Parkinson disease. Archives of Neurology, 60 (7). pp. 975-980.

Matteelli, A., Gori, A., Pinsi, G., El-Hamad, I., Bombana, E., Mastaglia, F., Degli Esposti, A., Bandera, A., Tedoldi, S., Casalini, C., Scolari, C., Carvalho, A.C.C. and Carosi, G. (2003) Clustering of tuberculosis among Senegalese immigrants in Italy. The International Journal of Tuberculosis and Lung Disease, 7 (10). pp. 967-972.

Cala, L.A., Parker, K., Emelyanova, I., Hicks, N., Robbins, P., Attikiouzel, Y., Michalak, K., Devenish, J., Kosek, J. and Mastaglia, F.L. (2003) Computer-Assisted Diagnosis of cranial CT scans. Rivista di Neuroradiologia, 16 (5). pp. 947-952.

Thickbroom, G.W., Byrnes, M.L. and Mastaglia, F.L. (2003) Dual representation of the hand in the cerebellum: Activation with voluntary and passive finger movement. NeuroImage, 18 (3). pp. 670-674.

van der Walt, J.M., Martin, E.R., Scott, W.K., Zhang, F., Nance, M.A., Watts, R.L., Hubble, J.P., Haines, J.L., Koller, W.C., Lyons, K., Pahwa, R., Stern, M.B., Colcher, A., Hiner, B.C., Jankovic, J., Ondo, W.G., Allen, F.H., Goetz, C.G., Small, G.W., Mastaglia, F., Roses, A.D., Stajich, J.M., Booze, M.W., Fujiwara, K., Gibson, R.A., Middleton, L.T., Scott, B.L., Pericak-Vance, M.A. and Vance, J.M. (2003) Genetic polymorphisms of the N-acetyltransferase genes and risk of Parkinson's disease. Neurology, 60 (7). pp. 1189-1191.

Li, Y-J, Oliveira, S.A., Xu, P., Martin, E.R., Stenger, J.E., Scherzer, C.R., Hauser, M.A., Scott, W.K., Small, G.W., Nance, M.A., Watts, R.L., Hubble, J.P., Koller, W.C., Pahwa, R., Stern, M.B., Hiner, B.C., Jankovic, J., Goetz, C.G., Mastaglia, F., Middleton, L.T., Roses, A.D., Saunders, A.M., Schmechel, D.E., Gullans, S.R., Haines, J.L., Gilbert, J.R., Vance, J.M. and Pericak-Vance, M.A. (2003) Glutathione S-transferase omega-1 modifiesage-at-onset of Alzheimer disease and Parkinson disease. Human Molecular Genetics, 12 (24). pp. 3259-3267.

Mastaglia, F.L., Garlepp, M.J., Phillips, B.A. and Zilko, P.J. (2003) Inflammatory myopathies: Clinical, diagnostic and therapeutic aspects. Muscle & Nerve, 27 (4). pp. 407-425.

Mastaglia, F.L. and Zilko, P.J. (2003) Inflammatory myopathies: How to treat the difficult cases. Journal of Clinical Neuroscience, 10 (1). pp. 99-101.

van der Walt, J.M., Nicodemus, K.K., Martin, E.R., Scott, W.K., Nance, M.A., Watts, R.L., Hubble, J.P., Haines, J.L., Koller, W.C., Lyons, K., Pahwa, R., Stern, M.B., Colcher, A., Hiner, B.C., Jankovic, J., Ondo, W.G., Allen Jr., F.H., Goetz, C.G., Small, G.W., Mastaglia, F., Stajich, J.M., McLaurin, A.C., Middleton, L.T., Scott, B.L., Schmechel, D.E., Pericak-Vance, M.A. and Vance, J.M. (2003) Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease. The American Journal of Human Genetics, 72 (4). pp. 804-811.

Oliveira, S.A., Scott, W.K., Martin, E.R., Nance, M.A., Watts, R.L., Hubble, J.P., Koller, W.C., Pahwa, R., Stern, M.B., Hiner, B.C., Ondo, W.G., Allen, F.H., Scott, B.L., Goetz, C.G., Small, G.W., Mastaglia, F., Stajich, J.M., Zhang, F., Booze, M.W., Winn, M.P., Middleton, L.T., Haines, J.L., Pericak-Vance, M.A. and Vance, J.M. (2003) Parkin mutations and susceptibility alleles in late-onset Parkinson's disease. Annals of Neurology, 53 (5). pp. 624-629.

Mastaglia, F.L., Johnsen, R.D., Byrnes, M.L. and Kakulas, B.A. (2003) Prevalence of amyloid-β deposition in the cerebral cortex in Parkinson's disease. Movement Disorders, 18 (1). pp. 81-86.

Mastaglia, F.L., Byrnes, M.L., Johnsen, R.D. and Kakulas, B.A. (2003) Prevalence of cerebral vascular amyloid-β deposition and stroke in an aging Australian population: A postmortem study. Journal of Clinical Neuroscience, 10 (2). pp. 186-189.

Thickbroom, G.W., Byrnes, M.L., Stell, R. and Mastaglia, F.L. (2003) Reversible reorganisation of the motor cortical representation of the hand in cervical dystonia. Movement Disorders, 18 (4). pp. 395-402.

Thickbroom, G.W., Byrnes, M.L., Blacker, D.J., Morris, I.T. and Mastaglia, F.L. (2003) A functional MRI protocol for localizing language comprehension in the human brain. Brain Research Protocols, 10 (3). pp. 175-180.

Gommans, I.M.P., Davis, M., Saar, K., Lammens, M., Mastaglia, F., Lamont, P., van Duijnhoven, G., ter Laak, J., Reis, A., Vogels, O.J.M., Laing, N., van Engelen, B.G.M. and Kremer, H. (2003) A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core-like lesions. Brain, 126 (7). pp. 1545-1551.

Gommans, I.M.P., Davis, M., Saar, K., Lammens, M., Mastaglia, F., Lamont, P., van Duijnhoven, G., ter Laak, J., Reis, A., Vogels, O.J.M., Laing, N., van Engelen, B.G.M. and Kremer, H. (2003) A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core‐like lesions. Brain, 126 (9). p. 2115.

Li, Y-J, Scott, W.K., Hedges, D.J., Zhang, F., Gaskell, P.C., Nance, M.A., Watts, R.L., Hubble, J.P., Koller, W.C., Pahwa, R., Stern, M.B., Hiner, B.C., Jankovic, J., Allen, F.H., Goetz, C.G., Mastaglia, F., Stajich, J.M., Gibson, R.A., Middleton, L.T., Saunders, A.M., Scott, B.L., Small, G.W., Nicodemus, K.K., Reed, A.D., Schmechel, D.E., Welsh-Bohmer, K.A., Conneally, P.M., Roses, A.D., Gilbert, J.R., Vance, J.M., Haines, J.L. and Pericak-Vance, M.A. (2002) Age at onset in two common neurodegenerative diseases is genetically controlled. The American Journal of Human Genetics, 70 (4). pp. 985-993.

Mastaglia, F.L., Phillips, B.A., Cala, L.A., Meredith, C., Egli, S., Akkari, P.A. and Laing, N.G. (2002) Early onset chromosome 14-linked distal myopathy (Laing). Neuromuscular Disorders, 12 (4). pp. 350-357.

Mastaglia, F.L. and Phillips, B.A. (2002) Idiopathic inflammatory myopathies: Epidemiology, classification, and diagnostic criteria. Rheumatic Disease Clinics of North America, 28 (4). pp. 723-741.

Thickbroom, G.W., Byrnes, M.L., Archer, S.A. and Mastaglia, F.L. (2002) Motor outcome after subcortical stroke: MEPs correlate with hand strength but not dexterity. Clinical Neurophysiology, 113 (12). pp. 2025-2029.

Mastaglia, F.L., Johnsen, R.D. and Kakulas, B.A. (2002) Prevalence of stroke in Parkinson's disease: A postmortem study. Movement Disorders, 17 (4). pp. 772-774.

Edwards, D.J., Thickbroom, G.W., Byrnes, M.L., Ghosh, S. and Mastaglia, F.L. (2002) Reduced corticomotor excitability with cyclic passive movement: A study using Transcranial Magnetic Stimulation. Human Movement Science, 21 (5-6). pp. 533-540.

Phillips, B.A., Zilko, P.J., Garlepp, M.J. and Mastaglia, F.L. (2002) Seasonal occurrence of relapses in inflammatory myopathies: A preliminary study. Journal of Neurology, 249 (4). pp. 441-444.

Haynes, M.J., Cala, L.A., Melsom, A., Mastaglia, F.L., Milne, N. and McGeachie, J.K. (2002) Vertebral arteries and cervical rotation: Modeling and magnetic resonance angiography studies. Journal of Manipulative and Physiological Therapeutics, 25 (6). pp. 370-383.

Martin, E.R., Scott, W.K., Nance, M.A., Watts, R.L., Hubble, J.P., Koller, W.C., Lyons, K., Pahwa, R., Stern, M.B., Colcher, A., Hiner, B.C., Jankovic, J., Ondo, W.G., Allen, F.H., Goetz, C.G., Small, G.W., Masterman, D., Mastaglia, F., Laing, N.G., Stajich, J.M., Ribble, R.C., Booze, M.W., Rogala, A., Hauser, M.A., Zhang, F., Gibson, R.A., Middleton, L.T., Roses, A.D., Haines, J.L., Scott, B.L., Pericak-Vance, M.A. and Vance, J.M. (2001) Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease. Journal of the American Medical Association, 286 (18). pp. 2245-50.

Scott, W.K., Nance, M.A., Watts, R.L., Hubble, J.P., Koller, W.C., Lyons, K., Pahwa, R., Stern, M.B., Colcher, A., Hiner, B.C., Jankovic, J., Ondo, W.G., Allen, Jr, F.H., Goetz, C.G., Small, G.W., Masterman, D., Mastaglia, F., Laing, N.G., Stajich, J.M., Slotterbeck, B., Booze, M.W., Ribble, R.C., Rampersaud, E., West, S.G., Gibson, R.A., Middleton, L.T., Roses, A.D., Haines, J.L., Scott, B.L., Vance, J.M. and Pericak-Vance, M.A. (2001) Complete genomic screen in Parkinson Disease. Journal of the American Medical Association, 286 (18). pp. 2239-2244.

Mastaglia, F.L., Thickbroom, G.W., Day, T. and Bond, R. (2001) Craniocervical tetanus presenting with dysphagia. Diagnostic value of electrophysiological studies. Journal of Neurology, 248 (10). pp. 903-904.

Thickbroom, G.W., Byrnes, M.L., Archer, S.A., Nagarajan, L. and Mastaglia, F.L. (2001) Differences in sensory and motor cortical organization following brain injury early in life. Annals of Neurology, 49 (3). pp. 320-327.

Byrnes, M.L., Thickbroom, G.W., Phillips, B.A. and Mastaglia, F.L. (2001) Long-term changes in motor cortical organisation after recovery from subcortical stroke. Brain Research, 889 (1-2). pp. 278-287.

Phillips, B.A., Cala, L.A., Thickbroom, G.W., Melsom, A., Zilko, P.J. and Mastaglia, F.L. (2001) Patterns of muscle involvement in inclusion body myositis: Clinical and magnetic resonance imaging study. Muscle & Nerve, 24 (11). pp. 1526-1534.

Garleep, M.J. and Mastaglia, F.L. (2000) Autoantibodies in inflammatory myopathies. American Journal of Medical Sciences, 319 (4). pp. 227-233.

Sacco, P., Thickbroom, G.W., Byrnes, M.L. and Mastaglia, F.L. (2000) Changes in corticomotor excitability after fatiguing muscle contractions. Muscle & Nerve, 23 (12). pp. 1840-1846.

Ziman, M.R., Pelham, J.T., Mastaglia, F.L. and Kay, P.H. (2000) Characterization of the alternate allelic forms of human PAX7. Mammalian Genome, 11 (4). pp. 332-337.

Phillips, B.A. and Mastaglia, F.L. (2000) Exercise therapy in patients with myopathy. Current Opinion in Neurology, 13 (5). pp. 547-552.

Pearce, A.J., Thickbroom, G.W., Byrnes, M.L. and Mastaglia, F.L. (2000) Functional reorganisation of the corticomotor projection to the hand in skilled racquet player. Experimental Brain Research, 130 (2). pp. 238-243.

Phillips, B.A., Lo, S.K. and Mastaglia, F.L. (2000) Isokinetic and isometric torque values using a Kin-Com dynamometer in normal subjects aged 20 to 69 years. Isokinetics and Exercise Science, 8 (3). pp. 147-159.

Bohannon, R.W., Phillips, B.A., Lo, S.K. and Mastaglia, F.L. (2000) Make tests and proper muscle strength measurement. Archives of Physical Medicine and Rehabilitatio, 81 (10). pp. 1442-1443.

Kok, C.C., Boyt, A., Gaudieri, S., Martins, R., Askanas, V., Dalakas, M., Kiers, L., Mastaglia, F. and Garleep, M. (2000) Mitochondrial DNA variants in inclusion body myositis. Neuromuscular Disorders, 10 (8). pp. 604-611.

Phillips, B.A., Lo, S.K. and Mastaglia, F.L. (2000) Muscle force measured using “break” testing with a hand-held myometer in normal subjects aged 20 to 69 years. Archives of Physical Medicine and Rehabilitation, 81 (5). pp. 653-661.

Phillips, B.A., Zilko, P.J. and Mastaglia, F.L. (2000) Prevalence of sporadic inclusion body myositis in Western Australia. Muscle & Nerve, 23 (6). pp. 970-972.

Mastaglia, F.L. (2000) Tibial nerve entrapment in the popliteal fossa. Muscle & Nerve, 23 (12). pp. 1883-1886.

Mastaglia, F.L. (2000) Treatment of autoimmune inflammatory myopathies. Current Opinion in Neurology, 13 (5). pp. 507-509.

Thickbroom, G.W., Byrnes, M.L., Sacco, P., Ghosh, S., Morris, I.T. and Mastaglia, F.L. (2000) The role of the supplementary motor area in externally timed movement: The influence of predictability of movement timing. Brain Research, 874 (2). pp. 233-241.

House, A.K., Bell, R., House, J., Mastaglia, F.L., Kumar, A. and D'Antuono, M. (1999) Asymptomatic carotid artery stenosis associated with peripheral vascular disease: a prospective study. Cardiovascular Surgery, 7 (1). pp. 44-49.

Sacco, P., Hope, P.A.J., Thickbroom, G.W., Byrnes, M.L. and Mastaglia, F.L. (1999) Corticomotor excitability and perception of effort during sustained exercise in the chronic fatigue syndrome. Clinical Neurophysiology, 110 (11). pp. 1883-1891.

Thickbroom, G.W., Phillips, B.A., Morris, I., Byrnes, M.L., Sacco, P. and Mastaglia, F.L. (1999) Differences in functional magnetic resonance imaging of sensorimotor cortex during static and dynamic finger flexion. Experimental Brain Research, 126 (3). pp. 431-438.

Mastaglia, F.L. and Laing, N.G. (1999) Distal myopathies: Clinical and molecular diagnosis and classification. Journal of Neurology, Neurosurgery & Psychiatry, 67 (6). pp. 703-707.

Laing, N.G. and Mastaglia, F.L. (1999) INVITED REVIEW - Inherited skeletal muscle disorders. Annals of Human Biology, 26 (6). pp. 507-525.

Kok, C.C., Croager, E.J., Witt, C.S., Kiers, L., Mastaglia, F.L., Abraham, L.J. and Garlepp, M.J. (1999) Mapping of a candidate region for susceptibility to inclusion body myositis in the human major histocompatibility complex. Immunogenetics, 49 (6). pp. 508-516.

Thickbroom, G.W., Byrnes, M.L. and Mastaglia, F.L. (1999) Methodology and application of TMS mapping. Electroencephalography and Clinical Neurophysiology, Supp. 51 . pp. 48-54.

Mastaglia, F.L. (1999) Myotonic dystrophies - how many are there? Current Opinion in Neurology, 12 (5). pp. 491-492.

Mastaglia, F.L., Nowak, K.J., Stell, R., Phillips, B.A., Edmondston, J.E., Dorosz, S.M., Wilton, S.D., Hallmayer, J., Kakulas, B.A. and Laing, N.G. (1999) Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy. Journal of Neurology, Neurosurgery & Psychiatry, 67 (2). pp. 174-179.

Byrnes, M.L., Thickbroom, G.W., Phillips, B.A., Wilson, S.A. and Mastaglia, F.L. (1999) Physiological studies of the corticomotor projection to the hand after subcortical stroke. Clinical Neurophysiology, 110 (3). pp. 487-498.

Thickbroom, G.W., Byrnes, M.L. and Mastaglia, F.L. (1999) A model of the effect of MEP amplitude variation on the accuracy of TMS mapping. Clinical Neurophysiology, 110 (5). pp. 941-943.

Scott, W.K., Yamaoka, L.H., Stajich, J.M., Scott, B.L., Vance, J.M., Roses, A.D., Pericak-Vance, M.A., Watts, R.L., Nance, M., Hubble, J., Koller, W., Stern, M.B., Colcher, A., Allen Jr., F.H., Hiner, B.C., Jankovic, J., Ondo, W., Laing, N.G., Mastaglia, F., Goetz, C., Pappert, E., Small, G.W., Masterman, D., Haines, J.L., Davies, T.L. and Roses, A.D. (1999) The α-synuclein gene is not a major risk factor in familial Parkinson disease. Neurogenetics, 2 (3). pp. 191-192.

Mastaglia, F.L., Harker, N., Phillips, B.A., Day, T.J., Hankey, G.J., Laing, N.G., Fabian, V. and Kakulas, B.A. (1998) Dominantly inherited proximal myotonic myopathy and leukoencephalopathy in a family with an incidental CLCN1 mutation. Journal of Neurology, Neurosurgery & Psychiatry, 64 (4). pp. 543-547.

Phillips, B.A., Zilko, P., Garlepp, M.J. and Mastaglia, F.L. (1998) Frequency of relapses in patients with polymyositis and dermatomyositis. Muscle & Nerve, 21 (12). pp. 1668-1672.

Mastaglia, F.L., Phillips, B.A. and Zilko, P.J. (1998) Immunoglobulin therapy in inflammatory myopathies. Journal of Neurology, Neurosurgery & Psychiatry, 65 (1). pp. 107-110.

Thickbroom, G.W., Phillips, B.A., Morris, I., Byrnes, M.L. and Mastaglia, F.L. (1998) Isometric force-related activity in sensorimotor cortex measured with functional MRI. Experimental Brain Research, 121 (1). pp. 59-64.

Thickbroom, G.W., Sammut, R. and Mastaglia, F.L. (1998) Magnetic stimulation mapping of motor cortex: Factors contributing to map area. Electroencephalography and Clinical Neurophysiology/Electromyography and Motor Control, 109 (2). pp. 79-84.

Tsai, C.H., Semmler, J.G., Kimber, T.E., Thickbroom, G., Stell, R., Mastaglia, F.L. and Thompson, P.D. (1998) Modulation of primary orthostatic tremor by magnetic stimulation over the motor cortex. Journal of Neurology, Neurosurgery & Psychiatry, 64 (1). pp. 33-36.

Taylor, B.V., Phillips, B.A., Speed, B.R., Kaldor, J., Carroll, W.M. and Mastaglia, F.L. (1998) Serological evidence for infection with Campylobacter jejuni/coli in patients with multifocal motor neuropathy. Journal of Clinical Neuroscience, 5 (1). pp. 33-35.

Byrnes, M.L., Thickbroom, G.W., Wilson, S.A., Sacco, P., Shipman, J.M., Stell, R. and Mastaglia, F.L. (1998) The corticomotor representation of upper limb muscles in writer's cramp and changes following botulinum toxin injection. Brain, 121 (5). pp. 977-988.

Pearce, A.J., Sacco, P., Byrnes, M.L., Thickbroom, G.W. and Mastaglia, F.L. (1998) The effects of eccentric exercise on neuromuscular function of the biceps brachll. Journal of Science and Medicine in Sport, 1 (4). pp. 236-244.

Sacco, P., Thickbroom, G.W., Thompson, M.L. and Mastaglia, F.L. (1997) Changes in corticomotor excitation and inhibition during prolonged submaximal muscle contractions. Muscle & Nerve, 20 (9). pp. 1158-1166.

Thompson, M.L., Thickbroom, G.W. and Mastaglia, F.L. (1997) Corticomotor representation of the sternocleidomastoid muscle. Brain, 120 (2). pp. 245-255.

Zilko, P.J., Mastaglia, F.L. and Phillips, B.A. (1997) Idiopathic Inflammatory Myopathies. BioDrugs, 7 (4). pp. 262-272.

Mastaglia, F.L., Phillips, B.A. and Zilko, P. (1997) Treatment of inflammatory myopathies. Muscle & Nerve, 20 (6). pp. 651-664.

Cunnington, R., Iansek, R., Thickbroom, G.W., Laing, B.A., Mastaglia, F.L., Bradshaw, J.L. and Phillips, J.G. (1996) Effects of magnetic stimulation over supplementary motor area on movement in Parkinson's disease. Brain, 119 (3). pp. 815-822.

Garlepp, M.J. and Mastaglia, F.L. (1996) Inclusion body myositis. Journal of Neurology, Neurosurgery & Psychiatry, 60 (3). pp. 251-255.

Fox, S.A., Ward, B.K., Robbins, P.D., Mastaglia, F.L. and Swanson, N.R. (1996) Inclusion body myositis: Investigation of the mumps virus hypothesis by polymerase chain reaction. Muscle & Nerve, 19 (1). pp. 23-28.

Mastaglia, F.L. and Laing, N.G. (1996) Investigation of muscle disease. Journal of Neurology, Neurosurgery & Psychiatry, 60 (3). pp. 256-274.

Garlepp, M.J. and Mastaglia, F.L. (1996) Reply (Letter). Annals of Neurology, 40 (2). pp. 264-265.

Wilson, S.A., Day, B.L., Thickbroom, G.W. and Mastaglia, F.L. (1996) Spatial differences in the sites of direct and indirect activation of corticospinal neurones by magnetic stimulation. Electroencephalography and Clinical Neurophysiology/Electromyography and Motor Control, 101 (3). pp. 255-261.

Thickbroom, G.W., Stell, R. and Mastaglia, F.L. (1996) Transcranial magnetic stimulation of the human frontal eye field. Journal of the Neurological Sciences, 144 (1-2). pp. 114-118.

Garlepp, M.J., Tabarias, H., van Bockxmeer, F.M., Zilko, P.J., Laing, B. and Mastaglia, F.L. (1995) Apolipoprotein E ϵ4 in inclusion body myositis. Annals of Neurolog, 38 (6). pp. 957-959.

Laing, N.G., Laing, B.A., Meredith, C., Wilton, S.D., Robbins, P., Honeyman, K., Dorosz, S., Kozman, H., Mastaglia, F.L. and Kakulas, B.A. (1995) Autosomal dominant distal myopathy: Linkage to chromosome 14. American Journal of Human Genetics, 56 (2). pp. 422-427.

Laing, B.A., Mastaglia, F.L., Lo, S.K. and Zilko, P. (1995) Comparative assessment of knee strength using Hand-Held myometry and isometric dynamometry in patients with inflammatory myopathy. Physiotherapy Theory and Practice, 11 (3). pp. 151-156.

Wilson, S.A., Thickbroom, G.W. and Mastaglia, F.L. (1995) Comparison of the magnetically mapped corticomotor representation of a muscle at rest and during low-level voluntary contraction. Electroencephalography and Clinical Neurophysiology/Electromyography and Motor Control, 97 (5). pp. 246-250.

Taylor, B.V. and Mastaglia, F.L. (1995) Guillain-Barré syndrome complicating treatment with streptokinase. Medical Journal of Australia, 162 (4). pp. 214-215.

Swanson, N.R., Fox, S.A. and Mastaglia, F.L. (1995) Search for persistent infection with poliovirus or other enteroviruses in amyotrophic lateral sclerosis-motor neurone disease. Neuromuscular Disorders, 5 (6). pp. 457-465.

Stell, R., Thickbroom, G.W. and Mastaglia, F.L. (1995) The audiogenic startle response in Tourette's syndrome. Movement Disorders, 10 (6). pp. 723-730.

Wilson, S.A., Thickbroom, G.W. and Mastaglia, F.L. (1995) An investigation of the late excitatory potential in the hand following magnetic stimulation of the motor cortex. Electroencephalography and Clinical Neurophysiology/Electromyography and Motor Control, 97 (1). pp. 55-62.

Sammut, R., Thickbroom, G.W., Wilson, S.A. and Mastaglia, F.L. (1995) The origin of the soleus late response evoked by magnetic stimulation of human motor cortex. Electroencephalography and Clinical Neurophysiology/Electromyography and Motor Control, 97 (3). pp. 164-168.

Swanson, N.R., Fox, S.A. and Mastaglia, F.L. (1994) Enterovirus hypothesis for motor neurone disease. British Medical Journal, 309 (6956). p. 743.

Garlepp, M.J., Laing, B., Zilko, P.J., OLLIER, W. and Mastaglia, F.L. (1994) HLA associations with inclusion body myositis. Clinical & Experimental Immunology, 98 (1). pp. 40-45.

Fox, S.A., Finklestone, E., Robbins, P.D., Mastaglia, F.L. and Swanson, N.R. (1994) Search for persistent enterovirus infection of muscle in inflammatory myopathies. Journal of the Neurological Sciences, 125 (1). pp. 70-76.

Laing, N.G., Laing, B.A., Meredith, C., Wilton, S.D., Mastaglia, F.L., Robbins, P., Honeyman, K., Dorosz, S. and Kakulas, B.A. (1993) Autosomal dominant distal myopathy: linkage to chromosome 14. Clinical Biochemist Reviews, 14 .

Kermode, A.G., Laing, B.A., Carroll, W.M. and Mastaglia, F.L. (1993) Immunoglobulin therapy. Neurology, 43 (12). p. 2727.

Sudoyo, H., Marzuki, S., Byrne, E. and Mastaglia, F. (1993) Phenotypic expression of mtDNA heteroplasmy in the skeletal muscle of patients with oculomyopathy: Defect in mitochondrial protein synthesis. Journal of the Neurological Sciences, 117 (1-2). pp. 83-91.

Wilson, S.A., Thickbroom, G.W. and Mastaglia, F.L. (1993) Topography of excitatory and inhibitory muscle responses evoked by transcranial magnetic stimulation in the human motor cortex. Neuroscience Letters, 154 (1-2). pp. 52-56.

Wilson, S.A., Thickbroom, G.W. and Mastaglia, F.L. (1993) Transcranial magnetic stimulation mapping of the motor cortex in normal subjects. Journal of the Neurological Sciences, 118 (2). pp. 134-144.

Mastaglia, F.L., Laing, B.A. and Zilko, P. (1993) Treatment of inflammatory myopathies. Bailliere's clinical neurology, 2 (3). pp. 717-740.

Wilson, S.A., Lockwood, R.J., Thickbroom, G.W. and Mastaglia, F.L. (1993) The muscle silent period following transcranial magnetic cortical stimulation. Journal of the Neurological Sciences, 114 (2). pp. 216-222.

Thickbroom, G.W. and Mastaglia, F.L. (1992) Cortical activity preceding self-initiated and externally triggered voluntary movement. Movement Disorders, 7 (4). p. 390.

Kermode, A.G., Laing, B.A., Carroll, W.M. and Mastaglia, F.L. (1992) Intravenous immunoglobulin for multifocal motor neuropathy. The Lancet, 340 (8824). pp. 920-921.

Kermode, A.G., Chakera, T. and Mastaglia, F.L. (1992) Low osmolar and non-ionic X-ray contrast media and cortical blindness. Clinical and Experimental Neurology, 29 . pp. 272-276.

Sudoyo, H., Marzuki, S., Mastaglia, F. and Carroll, W. (1992) Molecular genetics of Leber's hereditary optic neuropathy: Study of a six-generation family from Western Australia. Journal of the Neurological Sciences, 108 (1). pp. 7-17.

Scrimgeour, E.M., Mastaglia, F.L. and Kevau, I. (1992) Spinal muscular atrophy and probable Duchenne muscular dystrophy occurring separately in closely related Melanesian families in Papua, New Guinea. American Journal of Medical Genetics Part A, 43 (6). pp. 1044-1045.

Churchyard, A., Stell, R. and Mastaglia, F.L. (1991) Ataxia telangiectasia presenting as an extrapyramidal movement disorder and ocular motor apraxia without overt telangiectasia. Clinical and Experimental Neurology, 28 . pp. 90-96.

Trounce, I., Byrne, E., Marzuki, S., Dennett, X., Sudoyo, H., Mastaglia, F. and Berkovic, S.F. (1991) Functional respiratory chain studies in subjects with chronic progressive external ophthalmoplegia and large heteroplasmic mitochondrial DNA deletions. Journal of the Neurological Sciences, 102 (1). pp. 92-99.

Churchyard, A., Day, T., Grainger, K. and Mastaglia, F.L. (1991) Intravenous immunoglobulin therapy in the inflammatory neuropathies. Clinical and Experimental Neurology, 28 . pp. 168-179.

Thickbroom, G.W., Knezevicˇ, W., Carroll, W.M. and Mastaglia, F.L. (1991) Saccade onset and offset lambda waves: Relation to pattern movement visually evoked potentials. Brain Research, 551 (1-2). pp. 150-156.

Panegyres, P.K., Mastaglia, F.L. and Kakulas, B.A. (1990) Limb girdle syndromes: Clinical, morphological and electrophysiological studies. Journal of the Neurological Sciences, 95 (2). pp. 201-218.

Thickbroom, G.W. and Mastaglia, F.L. (1990) Premotor negativity associated with saccadic eye movement and finger movement: A comparative study. Brain Research, 506 (2). pp. 223-226.

Carroll, W.M., Jennings, A.R. and Mastaglia, F.L. (1990) The origin of remyelinating oligodendrocytes in antiserum-mediated demtelinative optic neuropathy. Brain, 113 (4). pp. 953-973.

Mastaglia, F.L., Masters, C.L., Beyreuther, K. and Kakulas, B.A. (1989) Deposition of Alzheimer's disease amyloid (A4) protein in the cerebral cortex in Parkinson's disease. Progress in clinical and biological research, 317 . pp. 475-484.

Panegyres, P.K. and Mastaglia, F.L. (1989) Guillain-Barre syndrome with involvement of the central and autonomic nervous systems. Medical Journal of Australia, 150 (11). pp. 655-659.

Willén, J.G., Griffiths, E.R., Mastaglia, F.L. and Beaver, R. (1989) Intermittent parasympathetic symptoms in lumbar spinal stenosis. Journal of Spinal Disorders, 2 (2). pp. 109-113.

Mastaglia, F.L., Carroll, W.M. and Jennings, A.R. (1989) Spinal cord lesions induced by antigalactocerebroside serum. Clinical and Experimental Neurology, 26 . pp. 33-44.

McNabb, A.W., Carroll, W.M. and Mastaglia, F.L. (1988) "Alien hand" and loss of bimanual coordination after dominant anterior cerebral artery territory infarction. Journal of Neurology, Neurosurgery & Psychiatry, 51 (2). pp. 218-222.

Mastaglia, F.L., Ojeda, V.J., Sarnat, H.B. and Kakulas, B.A. (1988) Myopathies associated with hypothyroidism: A review based upon 13 cases. Australian and New Zealand Journal of Medicine, 18 (6). pp. 799-806.

Day, T.J., Fisher, A.G. and Mastaglia, F.L. (1987) Alexia with agraphia in multiple sclerosis. Journal of the Neurological Sciences, 78 (3). pp. 343-348.

Knezevicˇ, W., Mastaglia, F.L., Thickbroom, G.W. and Carroll, W.M. (1987) Crossed facilitation and post-contraction depression of abductor pollicis brevis motor neurons. Clinical and Experimental Neurology, 23 . pp. 15-21.

Stuckey, B.G.A., Mastaglia, F.L., Reed, W.D. and Pullan, P.T. (1987) Glucocorticoid insufficiency, Achalasia, Alacrima with autonomic and motor neuropathy. Annals of Internal Medicine, 106 (1). pp. 62-64.

Thickbroom, G.W. and Mastaglia, F.L. (1987) Presaccadic spike potential: A computer model based upon motor unit recruitment patterns in the extraocular muscles. Brain Research, 422 (2). pp. 377-380.

Carroll, W.M., Jennings, A.R. and Mastaglia, F.L. (1987) Reactive glial cells in CNS demyelination contain both GC and GFAP. Brain Research, 411 (2). pp. 364-369.

Thompson, P.D., Mastaglia, F.L. and Carroll, W.M. (1986) Anterior ischaemic optic neuropathy. A correlative clinical and visual evoked potential study of 18 patients. Journal of Neurology, Neurosurgery & Psychiatry, 49 (2). pp. 128-135.

Thickbroom, G.W., Davies, H.D., Carroll, W.M. and Mastaglia, F.L. (1986) Averaging, spatio-temporal mapping and dipole modelling of focal epileptic spikes. Electroencephalography and Clinical Neurophysiology, 64 (3). pp. 274-277.

Steer, J.H., Mastaglia, F.L., Papadimitriou, J.M. and van Bruggen, I. (1986) Bupivacaine-induced muscle injury: The role of extracellular calcium. Journal of the Neurological Sciences, 73 (2). pp. 205-217.

Ojeda, V.J., Mastaglia, F.L. and Kakulas, B.A. (1986) Causes of organic dementia: A necropsy survey of 60 cases. Medical Journal of Australia, 145 (2). pp. 69-71.

Davies, H.D., Carroll, W.M. and Mastaglia, F.L. (1986) Effects of hyperventilation on pattern-reversal visual evoked potentials in patients with demyelination. Journal of Neurology, Neurosurgery & Psychiatry, 49 (12). pp. 1392-1396.

Day, T.J., Lefroy, R.B. and Mastaglia, F.L. (1986) Meige's syndrome and palatal myoclonus associated with brain stem stroke. A common mechanism? Journal of Neurology, Neurosurgery & Psychiatry, 49 (11). pp. 1324-1325.

Mastaglia, F.L. (1986) Musculocutaneous neuropathy after strenuous physical activity. Medical Journal of Australia, 145 (3-4). pp. 153-154.

Karagol, U., Gardner-Medwin, D. and Mastaglia, F.L. (1986) Neutrophil function in duchenne muscular dystrophy. Journal of the Neurological Sciences, 73 (1). pp. 73-77.

Thickbroom, G.W. and Mastaglia, F.L. (1986) Presaccadic spike potential. Relation to eye movement direction. Electroencephalography and Clinical Neurophysiology, 64 (3). pp. 211-214.

Steer, J.H. and Mastaglia, F.L. (1986) Protein degradation in bupivacaine-treated muscles. Journal of the Neurological Sciences, 75 (3). pp. 343-351.

Harvey, J.M., Zilko, P.J., Cheah, P.S., Mastaglia, F.L. and Ojeda, V.J. (1986) Scleromyxedema and inflammatory myopathy: A clinicopathology study of three patients. Australian and New Zealand Journal of Medicine, 16 (3). pp. 329-335.

Mastaglia, F.L., Knezevic, W and Thompson, P D (1986) Weakness of head turning in hemiplegia: A quantitative study. Journal of Neurology, Neurosurgery & Psychiatry, 49 (2). pp. 195-197.

Thickbroom, G.W. and Mastaglia, F.L. (1985) Cerebral events preceding self-paced and visually triggered saccades. A study of presaccadic potentials. Electroencephalography and Clinical Neurophysiology, 62 (4). pp. 277-289.

Thickbroom, G.W., Mastaglia, F.L., Carroll, W.M. and Davies, H.D. (1985) Cerebral potentials accompanying visually triggered finger movement in man. Electroencephalography and Clinical Neurophysiology/Evoked Potentials Section, 62 (3). pp. 209-218.

Day, T.J. and Mastaglia, F.L. (1985) Depot-glucagon in the treatment of McArdle's disease. Australian and New Zealand Journal of Medicine, 15 (6). pp. 748-750.

Thickbroom, G.W., Carroll, W.M. and Mastaglia, F.L. (1985) Dipole source derivation. Application to the half-field pattern evoked potential. International Journal of Bio-Medical Computing, 16 (1). pp. 17-28.

Carroll, W.M., Jennings, A.R. and Mastaglia, F.L. (1985) Galactocerebroside antiserum causes demyelination of cat optic nerve. Brain Research, 330 (2). pp. 378-381.

Mastaglia, F.L. and Ojeda, V.J. (1985) Inflammatory myopathies: Part 1. Annals of Neurology, 17 (3). pp. 215-227.

Mastaglia, F.L. and Ojeda, V.J. (1985) Inflammatory myopathies: Part 2. Annals of Neurology, 17 (4). pp. 317-323.

Ojeda, V.J., Frost, F. and Mastaglia, F.L. (1985) Non-bacterial thrombotic endocarditis associated with malignant disease: A clinicopathological study of 16 cases. Medical Journal of Australia, 142 (12). pp. 629-631.

Thickbroom, G.W. and Mastaglia, F.L. (1985) Presaccadic ‘spike’ potential: Investigation of topography and source. Brain Research, 339 (2). pp. 271-280.

Mastaglia, F.L. and Carroll, W.M. (1985) The effects of conditioning stimuli on the F-response. Journal of Neurology, Neurosurgery & Psychiatry, 48 (2). pp. 182-184.

Knezevicˇ, W., Mastaglia, F.L., Black, J.L. and Collins, D.W. (1984) Brainstem auditory evoked responses and quantitative saccade studies in multiple sclerosis: A comparative evaluation. Clinical and Experimental Neurology, 20 . pp. 175-179.

Thickbroom, G.W., Mastaglia, F.L. and Carroll, W.M. (1984) Computerised topographical mapping of scalp recorded event-related potentials. International Journal of Bio-Medical Computing, 15 (2). pp. 131-137.

Carroll, W.M., Jennings, A.R. and Mastaglia, F.L. (1984) Experimental demyelinating optic neuropathy induced by intra-neural injection of galactocerebroside antiserum. Journal of the Neurological Sciences, 65 (2). pp. 125-135.

Mastaglia, F.L., Carroll, W.M. and Thickbroom, G.W. (1984) F-response studies: Computer analysis and recovery cycle. Clinical and Experimental Neurology, 20 . pp. 217-223.

Joyce, D.A., Mastaglia, F.L., Ojeda, V.J. and Spagnolo, D.V. (1984) Familial myopathy associated with marfanoid features and multicores. Australian and New Zealand Journal of Medicine, 14 (4). pp. 495-499.

Knezevicˇ, W., Mastaglia, F.L., Quintner, J. and Zilko, P.J. (1984) Guillain-Barré syndrome and pemphigus foliaceus associated with D-penicillamine therapy. Australian and New Zealand Journal of Medicine, 14 (1). pp. 50-52.

Scrimgeour, E.M. and Mastaglia, F.L. (1984) Late-childhood-onset spinal muscular atrophy in three Melanesian families in Papua New Guinea. American Journal of Medical Genetics Part A, 19 (4). pp. 769-777.

Knezevicˇ, W., Mastaglia, F.L., Lefroy, R.B. and Fisher, A. (1984) Neuroleptic malignant syndrome. Medical Journal of Australia, 140 (1). pp. 28-30.

Knezevicˇ, W. and Mastaglia, F.L. (1984) Neuropathy associated With Brescia-Cimino arteriovenous fistulas. Archives of Neurology, 41 (11). pp. 1184-1186.

Scrimgeour, E.M. and Mastaglia, F.L. (1984) Oculopharyngeal and distal myopathy: A case study from papua new guinea. American Journal of Medical Genetics Part A, 17 (4). pp. 763-771.

Argov, Z., Gardner-Medwin, D., Johnson, M.A. and Mastaglia, F.L. (1984) Patterns of muscle Fiber-Type disproportion in hypotonic infants. Archives of Neurology, 41 (1). pp. 53-57.

Walker, G.L., Rosser, R., Mastaglia, F.L. and Walton, J.N. (1984) Psychometric and cranial CT study in myotonic dystrophy. Clinical and Experimental Neurology, 20 . pp. 161-167.

Thickbroom, G.W., Mastaglia, F.L., Carroll, W.M. and Davies, H.D. (1984) Source derivation: Application to topographic mapping of visual evoked potentials. Electroencephalography and Clinical Neurophysiology, 59 (4). pp. 279-285.

Thickbroom, G.W., Mastaglia, F.L. and Carroll, W.M. (1984) Spatio-temporal mapping of evoked cerebral activity. Electroencephalography and Clinical Neurophysiology/Evoked Potentials Section, 59 (6). pp. 425-431.

Johnson, M.A., Olmo, J.L. and Mastaglia, F.L. (1983) Changes in histochemical profile of rat respiratory muscles in hypo-and hyperthyroidism. Experimental Physiology, 68 . pp. 1-13.

Knezevicˇ, W. and Mastaglia, F.L. (1983) Digital gangrene caused by finger pricks made to obtain blood for blood glucose monitoring. Medical Journal of Australia, 2 (5). pp. 242-243.

Carroll, W.M., Jennings, A. and Mastaglia, F.L. (1983) Experimental demyelinating optic neuropathy: A model for combined morphological and electrophysiological studies. Clinical and Experimental Neurology, 19 . pp. 17-28.

Walker, G.L., Mastaglia, F.L., Lane, R.J. and Karagol, U. (1983) Immunological studies in myotonic dystrophy. Clinical and Experimental Neurology, 19 . pp. 29-36.

Walker, G., Karagol, U., Mathieson, E., Lane, R. and Mastaglia, F. (1983) Lymphocyte capping in myotonic dystrophy. Journal of Neurology, Neurosurgery & Psychiatry, 46 (1). pp. 90-92.

Mastaglia, F.L., McCallum, R.I. and Walder, D.N. (1983) Myelopathy associated with decompression sickness: A report of six cases. Clinical and Experimental Neurology, 19 . pp. 54-59.

Cala, L.A., Jones, B., Burns, P., Davis, R.E., Stenhouse, N. and Mastaglia, F.L. (1983) Results of computerized tomography, psychometric testing and dietary studies in social drinkers, with emphasis on reversibility after abstinence. Medical Journal of Australia, 2 (6). pp. 264-269.

Mastaglia, F.L. (1982) Adverse effects of drugs on muscle. Drugs, 24 (4). pp. 304-321.

Fawcett, P.R.W., McLachlan, S.M., Nicholson, L.V.B., Argov, Z. and Mastaglia, F.L. (1982) D-penicillamine-associated myasthenia gravis: Immunological and electrophysiological studies. Muscle & Nerve, 5 (4). pp. 328-334.

Fawcett, P.R.W., Mastaglia, F.L. and Mechler, F. (1982) Electrophysiological findings including single fibre EMG in a family with mitochondrial myopathy. Journal of the Neurological Sciences, 53 (2). pp. 397-410.

Mastaglia, F.L. and Carroll, W.M. (1982) Evoked potentials in neurological diagnosis. British Medical Journal (Clinical Research Ed.), 285 (6356). pp. 1678-1679.

Mastaglia, F.L. and Cala, L.A. (1982) Nuclear magnetic resonance imaging (NMR) and computerised tomography (CT) in multiple sclerosis. The Lancet, 319 (8276). p. 850.

Serisier, D.E., Mastaglia, F.L. and Gibson, G.J. (1982) Respiratory muscle function and ventilatory control I in patients with motor neurone disease II in patients with myotonic dystrophy. Quarterly Journal of Medicine, 51 (2). pp. 205-226.

Mastaglia, F.L., Black, J.L., Thickbroom, G. and Collins, D.W.K. (1982) Saccadic eye movements in multiple sclerosis*. Neuro-Ophthalmology, 2 (4). pp. 225-236.

Papadimtriou, J.M. and Mastaglia, F.L. (1982) Ultrastructural changes in human muscle fibres in disease. Journal of Submicroscopic Cytology, 14 (3). pp. 525-551.

Cala, L.A., Mastaglia, F.L., Jones, B. and Wiley, B. (1982) The effects of alcohol in social drinkers. Journal of Studies on Alcohol, 43 (5). pp. 614-615.

Walker, G.L., Mastaglia, F.L. and Roberts, D.F. (1982) A search for genetic influence in idiopathic inflammatory myopathy. Acta Neurologica Scandinavica, 66 (4). pp. 432-443.

Murakami, T., Mastaglia, F.L., Mann, D.M.A. and Bradley, W.G. (1981) Abnormal RNA metabolism in spinal motor neurons in the wobbler mouse. Muscle & Nerve, 4 (5). pp. 407-412.

Mechler, F. and Mastaglia, F.L. (1981) Adrenergic regulation of muscle blood flow in Becker's muscular dystrophy and dystrophia myotonica. Ideggyogyaszati Szemle (Clinical Neuroscience), 34 (9). pp. 398-404.

Cala, L.A., Thickbroom, G.W., Black, J.L., Collins, D.W. and Mastaglia, F.L. (1981) Brain density and cerebrospinal fluid space size: CT of normal volunteers. American Journal of Neuroradiology, 2 (1). pp. 41-47.

Livingstone, I.R., Mastaglia, F.L., Pennington, R.J.T. and Skilbeck, C. (1981) Choline chloride in the treatment of cerebellar and spinocerebellar ataxia. Journal of the Neurological Sciences, 50 (2). pp. 161-174.

Bateman, D.N., Bevan, P., Longley, B.P., Mastaglia, F. and Wandless, I. (1981) Cimetidine induced postural and action tremor. Journal of Neurology, Neurosurgery & Psychiatry, 44 (1). p. 94.

Mastaglia, F.L. (1981) Compression of the tibial nerve by the tendinous arch of origin of the soleus muscle. Clinical and Experimental Neurology, 18 . pp. 81-85.

Cala, L.A. and Mastaglia, F.L. (1981) Computerized tomography in chronic alcoholics. Alcoholism: Clinical and Experimental Research, 5 (2). pp. 283-294.

Livingstone, I., Johnson, M.A. and Mastaglia, F.L. (1981) Effects of dexamethasone on fibre subtypes in rat muscle. Neuropathology and Applied Neurobiology, 7 (5). pp. 381-398.

Melcher, F., Fawcett, P.R.W., Mastaglia, F.L. and Hudgson, P. (1981) Mitochondrial myopathy: A study of clinically affected and asymptomatic members of a six-generation family. Journal of Neurological Sciences, 50 (2). pp. 191-200.

Livingstone, I.R., Mastaglia, F.L., Edis, R. and Howe, J.W. (1981) Pattern visual evoked responses in hereditary spastic paraplegia. Journal of Neurology, Neurosurgery & Psychiatry, 44 (2). pp. 176-178.

Palmer, A.C., Calder, I.M., McCallum, R.I. and Mastaglia, F.L. (1981) Spinal cord degeneration in a case of "recovered" spinal decompression sickness. British Medical Journal, 283 (6296). p. 888.

Mechler, F. and Mastaglia, F.L. (1981) Vascular adrenergic receptor responses in skeletal muscle in myotonic dystrophy. Annals of Neurology, 9 (2). pp. 157-162.

Livingstone, I.R., Mastaglia, F.L., Edis, R. and Howe, J.W. (1981) Visual involvement in Friedreich's ataxia and hereditary spastic ataxia. Archives of Neurology, 38 (2). pp. 75-79.

Mechler, F., Mastaglia, F.L., Haggith, J. and Gardner-Medwin, D. (1980) Adrenergic receptor responses of vascular smooth muscle in Becker dystrophy. Journal of the Neurological Sciences, 46 (3). pp. 291-302.

Bajada, S., Mastaglia, F.L. and Fisher, A. (1980) Amyloid neuropathy and tremor in Waldenstrom's macroglobulinemia. Archives of Neurology, 37 (4). pp. 240-242.

Johnson, M.A., Mastaglia, F.L., Montgomery, A.G., Pope, B. and Weeds, A.G. (1980) Changes in myosin light chains in the rat soleus after thyroidectomy. FEBS Letters, 110 (2). pp. 230-235.

Mastaglia, F.L. and Cala, L.A. (1980) Computed tomography of the brain in multiple sclerosis. Trends in Neurosciences, 3 (1). pp. 16-20.

Cala, L.A. and Mastaglia, F.L. (1980) Computerized axial tomography in the detection of brain damage. 2. Epilepsy, migraine, and general medical disorders. Medical Journal of Australia, 2 (11). pp. 616-620.

Cala, L.A. and Mastaglia, F.L. (1980) Computerized axial tomography in the detection of brain damage: 1. Alcohol, nutritional deficiency and drugs of addiction. Medical Journal of Australia, 2 (4). pp. 193-198.

Argov, Z., Gardner-Medwin, D., Johnson, M.A. and Mastaglia, F.L. (1980) Congenital myotonic dystrophy. Archives of Neurology, 37 (11). pp. 693-696.

Mastaglia, F.L. (1980) Drug-induced disorders. Drug-induced disorders of muscle. British Journal of Hospital Medicine, 24 (1). 8 -16.

Bajada, S., Mastaglia, F.L., Black, J.L. and Collins, D.W. (1980) Effects of induced hyperthermia on visual evoked potentials and saccade parameters in normal subjects and multiple sclerosis patients. Journal of Neurology, Neurosurgery & Psychiatry, 43 (9). pp. 849-852.

Mastaglia, F.L., Black, J.L., Cala, L.A. and Collins, D.W.K. (1980) Electrophysiology and avoidance of invasive neuroradiology in multiple sclerosis. The Lancet, 315 (8160). p. 144.

Livingstone, I.R., Mastaglia, F.L., Howe, J.W. and Aherne, G.E. (1980) Leber's optic neuropathy: Clinical and visual evoked response studies in asymptomatic and symptomatic members of a 4-generation family. British Journal of Ophthalmology, 64 (10). pp. 751-757.

Mastaglia, F.L., Thompson, P.L. and Papadimitriou, J.M. (1980) Mitochondrial myopathy with cardiomyopathy, lactic acidosis and response to prednisone and thiamine. Australian and New Zealand Journal of Medicine, 10 (6). pp. 660-664.

Cullen, M.J. and Mastaglia, F.L. (1980) Morphological changes in dystrophic muscle. British Medical Bulletin, 36 (2). pp. 145-152.

Argov, Z., Nicholson, L., Fawcett, P.R.W., Mastaglia, F.L. and Hall, M. (1980) Neuromuscular transmission and acetylcholine receptor antibodies in rheumatoid arthritis patients on D-penicillamine. The Lancet, 315 (8161). p. 203.

Murakami, K., Mastaglia, F.L. and Bradley, W.G. (1980) Reduced protein synthesis in spinal anterior horn neurons in wobbler mouse mutant. Experimental Neurology, 67 (2). pp. 423-432.

Cala, L.A., Jones, B., Wiley, B. and Mastaglia, F.L. (1980) A computerised axial tomography (C.A.T.) study of alcohol induced cerebral atrophy-in conjuction with the other correlates. Acta Psychiatrica Scandinavica, 62 (Supp. s286). pp. 31-40.

Vita, G.F. and Mastaglia, F.L. (1980) The effects of thyroidectomy on the extraocular muscles of the rat: A histochemical study. Neuropathology and Applied Neurobiology, 6 (6). pp. 465-470.

Johnson, M.A., Mastaglia, F.L. and Montgomery, A. (1980) The histochemical and contractile properties of hyperthyroid mammalian skeletal muscle. IRCS Medical Science, 8 (10). p. 711.

Vita, G.F., Mastaglia, F.L. and Johnson, M.A. (1980) A histochemical study of fibre types in rat extraocular muscles. Neuropathology and Applied Neurobiology, 6 (6). pp. 449-463.

Livingstone, I.R., Mastaglia, F.L. and Pennington, R.J.T. (1980) An investigation of pyruvate metabolism in patients with cerebellar and spinocerebellar degeneration. Journal of the Neurological Sciences, 48 (1). pp. 123-132.

Murakami, T. and Mastaglia, F.L. (1979) Abnormal RNA turnover in wobbler mouse motor neurones. IRCS Medical Science, 7 (8). p. 416.

Carroll, W.M. and Mastaglia, F.L. (1979) Alpha and beta coma in drug intoxication uncomplicated by cerebral hypoxia. Electroencephalography and Clinical Neurophysiology, 46 (1). pp. 95-105.

Livingstone, I.R. and Mastaglia, F.L. (1979) Choline chloride in the treatment of ataxia. British Medical Journal, 2 (6195). p. 939.

Koch-Weser, J., Argov, Z. and Mastaglia, F.L. (1979) Disorders of neuromuscular transmission caused by drugs. New England Journal of Medicine, 301 (8). pp. 409-413.

Argov, Z. and Mastaglia, F.L. (1979) Drug-induced peripheral neuropathies. British Medical Journal, 1 (6164). pp. 663-666.

Carroll, W.M. and Mastaglia, F.L. (1979) Leber's optic neuropathy: A clinical and visual evoked potential study of affected and asymptomatic members of a six generation family. Brain, 102 (3). pp. 559-580.

Carroll, W.M. and Mastaglia, F.L. (1979) Optic neuropathy and ophthalmoplegia in herpes zoster oticus. Neurology, 29 (5). p. 726.

Mastaglia, F.L., Black, J.L. and Collins, D.W.K. (1979) Quantitative studies of saccadic and pursuit eye movements in multiple sclerosis. Brain, 102 (4). pp. 817-834.

Johnson, M.A., Mastaglia, F.L. and Montgomery, A. (1979) A neurally mediated effect of thyroid hormone on slow-twitch skeletal muscle? IRCS Medical Science, 7 (8). p. 415.

Cala, L.A., Jones, B., Mastaglia, F.L. and Wiley, B. (1978) Brain atrophy and intellectual impairment in heavy Drinkers-A clinical, psychometric and computerized tomography study. Australian and New Zealand Journal of Medicine, 8 (2). pp. 147-153.

Lane, R.J.M and Mastaglia, F.L. (1978) Drug-induced myopathies in man. The Lancet, 312 (8089). pp. 562-566.

Black, J.L. and Mastaglia, F.L. (1978) On-line electro-oculography. International Journal of Bio-Medical Computing, 9 (5). pp. 393-404.

Collins, D.W.K., Black, J.L. and Mastaglia, F.L. (1978) Pattern-reversal visual evoked potential. Journal of the Neurological Sciences, 36 (1). pp. 83-95.

Mastaglia, F.L., Black, J.L., Collins, D.W.K., Gutteridge, D.H. and Yuen, R.W.M. (1978) Slowing of conduction in visual pathway in hypothyroidism. The Lancet, 311 (8060). pp. 387-388.

Mastaglia, F.L., Black, J.L., Edis, R. and Collins, D.W. (1978) The contribution of evoked potentials in the functional assessment of the somatosensory pathway. Clinical and Experimental Neurology, 15 . pp. 279-298.

Cala, L.A. and Mastaglia, F.L. (1977) Computerised tomography findings in multiple sclerosis and Schilder's disease. Clinical and Experimental Neurology, 14 . pp. 229-236.

Cala, L.A., Mastaglia, F.L. and Woodings, T.L. (1977) Computerised tomography of the cranium in patients with epilepsy: A preliminary report. Clinical and Experimental Neurology, 14 . pp. 237-244.

Dawkins, R.L., Mastaglia, F.L. and Kay, P. (1977) Diagnostic significance of autoantibodies and HLA in myasthenia gravis and multiple sclerosis. Clinical and Experimental Neurology, 14 . pp. 122-124.

Mastaglia, F.L., Black, J.L., Cala, L.A. and Collins, D.W. (1977) Electrophysiological and computerised tomography findings in multiple sclerosis: a comparative study. Clinical and Experimental Neurology, 14 . pp. 223-228.

Mastaglia, F.L., Black, J.L., Cala, L.A. and Collins, D.W. (1977) Evoked potentials, saccadic velocities, and computerized tomography in diagnosis of multiple sclerosis. British Medical Journal, 1 (6072). pp. 1315-1317.

Carroll, W.M. and Mastaglia, F.L. (1977) Ocular motor involvement in post-infective polyneuropathy. Clinical and Experimental Neurology, 14 . pp. 66-74.

Carroll, W.M. and Mastaglia, F.L. (1977) Ocular motor involvement in post-infective polyneuropathy. Clinical and Experimental Neurology, 14 . pp. 66-74.

Black, J.L., Mastaglia, F.L. and Collins, D.W.K. (1977) Quantitative ocular kinetic studies using an on line computer. Electroencephalography and Clinical Neurophysiology, 43 (4).

Mastaglia, F.L., Black, J.L. and Collins, D.W.K. (1977) Saccadic and pursuit eye movements in patients with multiple sclerosis. Electroencephalography and Clinical Neurophysiology, 43 (4).

Mastaglia, F.L., Black, J.L., Collins, D.W. and Dawkins, R.L. (1977) Saccadic velocities in diagnosis of myasthenia gravis. The Lancet, 310 (8028). p. 83.

Mastaglia, F.L., Black, J.L. and Collins, D.W. (1977) Saccadic velocities in multiple sclerosis and myasthenia gravis. Clinical and Experimental Neurology, 14 . pp. 117-121.

Mastaglia, F.L., Papadimitriou, J.M., Dawkins, R.L. and Beveridge, B. (1977) Vacuolar myopathy associated with chloroquine, lupus erythematosus and thymoma. Journal of the Neurological Sciences, 34 (3). pp. 315-328.

Edis, R.H. and Mastaglia, F.L. (1977) Vertical gaze palsy in barbiturate intoxication. British Medical Journal, 1 (6054). p. 144.

Cala, L.A. and Mastaglia, F.L. (1976) Computerised axial tomography findings in patients with migrainous headaches. British Medical Journal, 2 (6028). pp. 149-150.

Cala, L.A. and Mastaglia, F.L. (1976) Computerized axial tomography findings in a group of patients with migrainous headaches. Proceedings of the Australian Association of Neurologists, 13 . pp. 35-41.

Mastaglia, F.L., McDonald, W.I., Watson, J.V. and Yogendran, K. (1976) Effects of X-Radiation on the spinal cord: An experimental study of the morphological changes in central nerve fibres. Brain, 99 (1). pp. 101-122.

Mastaglia, F.L., Black, J.L. and Collins, D.W.K. (1976) Evoked potential studies in neurological disorders. Proceedings of the Australian Association of Neurologists, 13 . pp. 15-23.

Cala, L.A., Mastaglia, F.L. and Vaughan, R.J (1976) Localisation of stereotactic radiofrequency thalamic lesions by computerised axial tomography. The Lancet, 308 (7995). pp. 1133-1134.

Mastaglia, F.L., McDonald, W.I. and Yogendran, K. (1976) Nodal changes during the early stages of Wallerian degeneration of central nerve fibres. Journal of the Neurological Sciences, 30 (2-3). pp. 259-267.

Grainger, K. and Mastaglia, F.L. (1976) Smoking, transient ischaemic attacks and stroke: A temporal association. Medical Journal of Australia, 2 (8). pp. 302-303.

Mastaglia, F.L., Black, J.L. and Collins, D.W.K. (1976) Visual and spinal evoked potentials in diagnosis of multiple sclerosis. British Medical Journal, 2 (6038). p. 732.

Black, J.L., Isele, D.F., Head, R.L, Fleming, I.R., Collins, D.W.K. and Mastaglia, F.L. (1976) A versatile averaging system for neurophysiology. Computers in Biology and Medicine, 6 (1). pp. 9-21.

Mastaglia, F.L., McDonald, W.I., Watson, J. and Yogendran, K. (1975) Early effects of X-irradiation on central nerve fibres. British Journal of Radiology, 48 (576). pp. 1042-1043.

Mastaglia, F.L. and Grainger, K.M.R. (1975) Internuclear ophthalmoplegia in progressive supranuclear palsy. Journal of the Neurological Sciences, 25 (3). pp. 303-308.

Mastaglia, F.L., Papadimitriou, J.M. and Dawkins, R.L. (1975) Mechanisms of cell-mediated myotoxicity. Journal of the Neurological Sciences, 25 (3). pp. 269-282.

Mastaglia, F.L., Dawkins, R.L. and Papadimitriou, J.M. (1975) Morphological changes in skeletal muscle after transplantation. Journal of the Neurological Sciences, 25 (2). pp. 227-247.

Mastaglia, F.L., Dawkins, R.L. and Papadimitriou, J.M. (1974) Lymphocyte-muscle cell interactions in vivo and in vitro. Journal of the Neurological Sciences, 22 (2). pp. 261-268.

Mastaglia, F.L., Grainger, M.R. and Kakulas, B.A. (1974) Palatal myoclonus and associated movements. Proceedings of the Australian Association of Neurologists, 11 . pp. 183-187.

Mastaglia, F.L. (1974) See-saw nystagmus: an unusual sign of brain-stem infarction. Journal of Neurological Sciences, 22 (4). pp. 439-443.

Dawkins, R.L. and Mastaglia, F.L. (1973) Cell-Mediated cytotoxicity to muscle in polymyositis. New England Journal of Medicine, 288 (9). pp. 434-438.

Mastaglia, F.L. (1973) Pathological changes in skeletal muscle in acromegaly. Acta Neuropathologica, 24 (4). pp. 273-286.

Mastaglia, F.L., Grainger, K., Kee, F., Sadka, M. and Lefroy, R. (1973) Progressive supranuclear palsy (the Steele-Richardson-Olszewski syndrome) clinical and electrophysiological observations in eleven cases. Proceedings of the Australian Association of Neurologists, 10 . pp. 35-44.

Mastaglia, F.L., Berger, L. and Kakulas, B.A. (1972) Globoid aneurysms of the cerebral vessels. Neurology India, 20 (Supp. 2). pp. 302-308.

Mastaglia, F.L. and Walton, J.N. (1971) Histological and histochemical changes in skeletal muscle from cases of chronic juvenile and early adult spinal muscular atrophy (the Kugelberg-Welander syndrome). Journal of the Neurological Sciences, 12 (1). pp. 15-44.

Mastaglia, F.L. and Currie, S. (1971) Immunological and ultrastructural observations on the role of lymphoid cells in the pathogenesis of polymyositis. Acta Neuropathologica, 18 (1). pp. 1-16.

Mastaglia, F.L., Gardner-Medwin, D. and Hudgson, P. (1971) Muscle fibrosis and contractures in a pethidine addict. British Medical Journal, 4 (5786). pp. 532-533.

Mastaglia, F.L., Savas, S., Kakulas, B.A. and Lekias, J.S. (1971) Thrombosis of the internal carotid artery after closed head injury. Proceedings of the Australian Association of Neurologists, 8 . pp. 93-100.

Mastaglia, F.L. and Walton, J.N. (1971) An electron microscopic study of skeletal muscle from cases of the Kugelberg-Welander syndrome. Acta Neuropathologica, 17 (3). pp. 201-219.

Mastaglia, F.L. and Walton, J.N. (1971) An ultrastructural study of skeletal muscle in polymyositis. Journal of the Neurological Sciences, 12 (4). pp. 473-504.

Mastaglia, F.L. and Walton, J.N. (1970) Coxsackie virus-like particles in skeletal muscle from a case of polymyositis. Journal of the Neurological Sciences, 11 (6). pp. 593-599.

Ross, K.F.A., Jans, D.E., Larson, P.F., Mastaglia, F.L., Parsons, R., Fulthorpe, J.J., Jenkison, M. and Walton, J.N. (1970) Distribution of Ribosomal RNA in Fusing Myoblasts. Nature, 226 (5245). pp. 545-547.

Mastaglia, F.L. and Kakulas, B.A. (1970) Intramedullary spinal cord metastasis from mammary carcinoma. Paraplegia, 8 (1). pp. 14-18.

Mastaglia, F.L., Papadimitriou, J.M. and Kakulas, B.A. (1970) Regeneration of muscle in Duchenne muscular dystrophy: An electron microscope study. Journal of the Neurological Sciences, 11 (5). pp. 425-444.

Mastaglia, F.L., McCollum, J.P., Larson, P.F. and Hudgson, P. (1970) Steroid myopathy complicating McArdle's disease. Journal of Neurology, Neurosurgery & Psychiatry, 33 (1). pp. 111-120.

Mastaglia, F.L. and Kakulas, B.A. (1970) A histological and histochemical study of skeletal muscle regeneration in polymyositis. Journal of the Neurological Sciences, 10 (5). pp. 471-487.

Rowlands, J.B., Mastaglia, F.L., Kakulas, B.A. and Hainsworth, D. (1969) Clinical and pathological aspects of a fatal case of mulga (Pseudechis australis) snakebite. Medical Journal of Australia, 1 (1). pp. 226-230.

Mastaglia, F.L., Savas, S. and Kakulas, B.A. (1969) Intracranial thrombosis of the internal carotid artery after closed head injury. Journal of Neurology, Neurosurgery & Psychiatry, 32 (5). pp. 383-388.

Mastaglia, F.L., Edis, B. and Kakulas, B.A. (1969) Medullary haemorrhage: A report of two cases. Journal of Neurology, Neurosurgery & Psychiatry, 32 (3). pp. 221-225.

Mastaglia, F.L., Papadimitriou, J.M. and Kakulas, B.A. (1969) Regeneration in Duchenne muscular dystrophy. A histological electron-microscopic and histochemical study. Proceedings of the Australian Association of Neurologists, 6 . pp. 93-106.

Mastaglia, F.L. and Kakulas, B.A. (1969) Regeneration in duchenne muscular dystrophy: A histological and histochemical study. Brain, 92 (4). pp. 809-818.

Mastaglia, F.L., Papadimitriou, J.M. and Kakulas, B.A. (1969) Restricted forms of muscular dystrophy: A study of 11 cases. Proceedings of the Australian Association of Neurologists, 6 . pp. 107-121.

Papadimitriou, J.M., Mastaglia, F.L. and Kakulas, B.A. (1969) The natural history of Duchenne muscular dystrophy--an ultrastructural study. Proceedings of the Australian Association of Neurologists, 6 . pp. 107-121.

Kakulas, B.A., Hamilton, G.J. and Mastaglia, F.L. (1968) Clinical and neuropathological observations in phenylketonuria. Proceedings of the Australian Association of Neurologists, 5 (1). pp. 155-158.

Kakulas, B.A., Papadimitriou, J.M., Knight, J.O. and Mastaglia, F.L. (1968) Normal and abnormal human muscle in tissue culture. Proceedings of the Australian Association of Neurologists, 5 (1). pp. 79-85.

Kakulas, B.A., Knight, J.O., Gubbay, S.S. and Mastaglia, F.L. (1968) The detection of female carriers of pseudohypertrophic muscular dystrophy. Proceedings of the Australian Association of Neurologists, 5 (3). pp. 545-551.

Mastaglia, F.L. and Kakulas, B.A. (1968) The natural history of human muscle diseases studied by means of serial biopsy. Proceedings of the Australian Association of Neurologists, 5 (3). pp. 537-543.

Mastaglia, F.L. and Kakulas, B.A. (1967) Rheumatoid arthritis, polyarteritis, polymyositis, gastritis and Hashimoto's thyroiditis. Medical Journal of Australia, 1 (22). pp. 1135-1136.

Kakulas, B.A. and Mastaglia, F.L. (1966) Type and incidence of lesions found in a human necropsy survey of skeletal muscle. Proceedings of the Australian Association of Neurologist, 4 . pp. 35-47.

Conference Paper

Thomson, K., Hammond, G., Anderson, M. and Mastaglia, F. (2003) The programming of sequential movements in individuals with Parkinson's Disease. In: Pre-conference Meeting of the APS College of Neuropsychologists, Melbourne, Victoria p. 159.

Michalak, K., Devenish, J., Linggard, R., Parker, K., Emelyanova, I., Cala, L., Attikiouzel, Y., Hicks, N., Robbins, P. and Mastaglia, F. (2002) Automated measurement of brain dimensions. In: Proceedings of the 7th International Conference on Control, Automation, Robotics and Vision, ICARC 2002, 2 - 5 December, Singapore pp. 525-529.

Devenish, J., Linggard, R., Michalak, K., Parker, K., Emelyanova, I., Cala, L., Attikiouzel, Y., Hicks, N., Robbins, P. and Mastaglia, F. (2002) Quantifying skull shape. In: Proceedings of the 7th International Conference on Control, Automation, Robotics and Vision, ICARCV 2002, 2 - 5 December, Singapore pp. 530-535.

Conference Item

Herrmann, S.E., Grace, A., McKinnon, E., Skinner, M.J., Locke, V., Correia, H., Byrnes, M., Chaney, R. and Mastaglia, F.L. (2016) Moving into the 50+ age demographic: A snapshot of neuropsychological health in a cohort of people living with chronic HIV infection. In: Australasian HIV AIDS Conference 2016, 16 - 18 November 2016, Adelaide, SA.

Herrmann, S., McKinnon, E., Grace, A., Locke, V., Correia, H., Byrnes, M., Chaney, R., Mastaglia, F. and Mallal, S. (2016) A snapshot of neuropsychological health in a “50-Something Aged” cohort of people living with chronic HIV infection. In: Australasian Sexual Health Conference (ASHM) 2016, 14 - 16 November 2016, Adelaide, Australia.

Mastaglia, F.L. (2014) Immune-mediated inflammatory myopathies. In: ANZAN 2014 Neurology Conference, 18 - 22 May 2014, Adelaide, SA.

Wilton, S.D., Fletcher, S. and Mastaglia, F.L. (2010) Evaluating new therapies & clinical trials: Why, when, which treatment and what benefit? In: MD2010 Conference: Connect, Learn, Share, 9 - 10 September 2010, Perth, Western Australia.

Needham, M., Scott, A., James, I., Day, T., Kiers, L., Corbett, A., Witt, C., Garlepp, M., Allcock, R., Laing, N., Christiansen, F. and Mastaglia, F. (2009) Epistatic interactions between alleles at the DRB1 locus influence both susceptibility to sIBM and clinical phenotype. In: World Muscle Society Congress, 9 - 12 September 2009, Geneva, Switzerland.

Wu, J., Qui, W., James, I., Joseph, J., Carroll, W., Christiansen, F., Mastaglia, F. and Kermode, A. (2009) Frequency of HLA-DRB1 alleles and disease-modifying effects in a large West Australian multiple sclerosis cohort. In: Australian & New Zealand Association of Neurologists Annual Scientific Meeting, 18 - 21 May 2009, Christchurch, New Zealand.

Laing, N.G., Mastaglia, F.L., Fabian, V., Jacob, R., Davis, M.R., Wilton, S.D., Morling, P., Papadimitriou, J.M., Valentine, J. and Kakulas, B.A. (1998) Genetic studies in a family with autosomal dominant rod and core disease. In: 3rd International Congress of World Muscle Society, 29 - 30 May 1998, Naples, Italy.

Book Chapter

O’Connor, K.D.J. and Mastaglia, F.L. (2014) Drug-Induced disorders of the nervous system. In: Aminoff, M.J. and Josephson, S.A., (eds.) Aminoff's Neurology and General Medicine. Academic Press, pp. 685-711.

Mastaglia, F.L. (2011) Sporadic inclusion-body myositis: Clinical symptoms, physical findings, and diagnostic investigations. In: Askanas, V. and Engel, W.K., (eds.) Muscle Aging, Inclusion-Body Myositis and Myopathies. Wiley-Blackwell, pp. 159-167.

Mastaglia, F.L. and Needham, M. (2010) Inclusion Body Myositis. In: Lisak, R.P., Truong, D.D., Carroll, W.M. and Bhidayasiri, R., (eds.) International Neurology. Wiley-Blackwell, pp. 474-476.

Mastaglia, F.L. (2008) Drug-Induced disorders of the nervous system. In: Aminoff, M.J., (ed.) Neurology and General Medicine. Churchill Livingstone Elsevier, Philadelphia, PA, pp. 695-719.

Sacco, P., Thickbroom, G.W. and Mastaglia, F.L. (2005) The Role of Transcranial Magnetic Stimulation in the Study of Fatigue. In: Hallett, M. and Chokroverty, S., (eds.) Magnetic Stimulation in Clinical Neurophysiology. Elsevier, Philadelphia, PA, pp. 211-222.

Garlepp, M.J., Blechynden, L., Tabarias, H., Lawson, C.M., Van Bockxmeer, F. and Mastaglia, F.L. (1998) Genetic factors in sporadic inclusion-body myositis. In: Askanas, V., Serratrice, G. and Engel, W.K., (eds.) Inclusion-Body Myositis and Myopathies. Cambridge University Press, Cambridge, pp. 177-188.

This list was generated on Wed Nov 22 03:20:52 2017 UTC.