2000 Research Publications

Neuromuscular and Neurological Disorders, Centre for

Books and Chapters

Mastaglia, F.L. and Reilly, M.M. Neuromuscular disease: muscle, UK, Lippincott Williams & Wilkins (2000)

Journal Articles

Fletcher, S., Wilton, S.D.and Howell, J.MCC. Gene therapy and molecular approaches to the treatment of hereditary muscular disorders, Current Opinion in Neurology, 13:5, pp 553-560 (2000)

Garlepp, M.J. and Mastaglia, F.L. Autoantibodies in Inflammatory Myopathies, The American Journal of the Medical Sciences, 319:4, pp 227-233 (2000)

Hentati, A., Warner, C., Laing, N.G., Cambi, F., Mitsumoto, H., Roos, R.P., Boustany, R.M., Hamida, M.B., Hentati, F., Siddique, T., Deng, H.X., Zhai, H., Chen, W., Yang, Y., Hung, W.Y., Azim, A.C., Bohlega, S. and Tandan, R. Novel mutations in spastin gene and absence of correlation with age at onset of symptoms, Neurology, 55: pp 1388-1390 (2000)

Kakulas, B.A. Milestones in myopathology, Acta Myologica, XIX: pp 193-200 (2000)

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

Lu, Q.L., Morris, G.E., Wilton, S.D., Ly, T., rtem’yeva, O.V., Strong, P. and Partridge, T.A. Massive idiosyncratic exon skipping corrects the nonsense mutation in dystrophic mouse muscle and produces functional revertant fibers by clonal expansion, The Journal of Cell Biology, 148:5, pp 985-995 (2000)

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

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

Mastaglia, F.L. Inclusion body myositis, World Neurology, 15:4, pp 9-10 (2000)

Nowak, K.J., Walsh, P., Jacob, R.L., Johnsen, R.D., Peverall, J., McNally, E.M., Wilton, S.D., Kakulas, B.A. and Laing, N.G. Severe g-sarcoglycanopathy caused by a novel missense mutation and a large deletion, Neuromuscular Disorders, 10: pp 100 -107 (2000)

Panegyres, P.K., Zafiris-Toufexis, K. and Kakulas, B.A. Amyloid precursor protein gene isoforms in Alzheimer’s disease and other neurodegenerative disorders, Journal of the Neurological Sciences, 173: pp 81-92 (2000)

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

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

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

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

Phillips, B.A., Lo, S.K. and Mastaglia, F.L. 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: pp 653-661 (2000)

Ro, J.Y., Debowy, D., Ghosh, S. and Gardner, E.P. Depression of neuronal firing rates in somatosensory and posterior parietal cortex during object acquisition in a prehension task, Experimental Brain Research, 135: pp 1-11 (2000)

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

Scacheri, P.C., Hoffman, E.P., Fratkin, J.D., Semino-Mora, C., Senchak, A., Davis, M.R., Laing, N.G., Vedanarayanan, V. and Subramony, S.H. A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathy, Neurology, 55: pp 1689-1696 (2000)

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

Wallgren-Petterson, C. and Laing, N.G. Report of the 70th ENMC International Workshop: Nemaline Myopathy, 11-13 June 1999, Naarden, The Netherlands, Neuromuscular Disorders, 10: pp 299-306 (2000)

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