Neuromuscular and Neurological Disorders, Centre forBooks and ChaptersSacco, P., Thickbroom, G.W. and Mastaglia, F.L. The Role of Transcranial Magnetic Stimulation in the Study of Fatigue, Magnetic Stimulation in Clinical Neurophysiology, ed Hallett, M. Chokroverty, S., United States, Elsevier Butterworth Heinemann, pp 211-222 (2005) Journal ArticlesBenwell, N.M., Byrnes, M.L., Mastaglia, F.L. and Thickbroom, G.W. Primary sensorimotor cortex activation with task-performance after fatiguing hand exercise, Experimental Brain Research, 167: pp 160-164 (2005) Byrnes, M.L., Mastaglia, F.L., Walters, S.E., Archer, S.R. and Thickbroom, G.W. Primary writing tremor: motor cortex reorganisation and disinhibition, Journal of Clinical Neuroscience, 12:1, pp 102-104 (2005) Corbett, M.A., Akkari, P.A., Domazetovska, A., Cooper, S.T., North, K.N., Laing, N.G., Gunning, P.W. and Hardeman, E.C. An αTropomysin Mutation Alters Dimer Preference in Nemaline Myopathy, Annals of Neurology, 57: pp 42-49 (2005) Gebski, B.L., Errington, S.J., Johnson, R.D., Fletcher, S. and Wilton, S.D. Terminal antisense oligonucleotide modifications can enhance induced exon skipping, Neuromuscular Disorders, 15: pp 622-629 (2005) Haynes, M.J., Cala, L.A., Melsom, A., Mastaglia, F.L., Milne, N. and McGeachie, J.K. 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: pp 323-329 (2005) Kakulas, B.A. In reply to J Silver, Spinal Cord, 43: p 327 (2005) Laing, N.G., Groote, C., Dye, D.E., Liyanage, K., Duff, R.M., Dubois, B., Robberecht, W., Sciot, R., Martin, J.J. and Goebel, H.H. Myosin storage myopathy: Slow skeletal myosin (MYH7) mutation in two isolated cases, Neurology, 64: pp 527-529 (2005) Mastaglia, F.L. Neuromuscular disorders: molecular and therapeutic insights, The Lancet Neurology, 4: pp 6-7 (2005) Mastaglia, F.L., Lamont, P.J. and Laing, N.G. Distal myopathies, Current Opinion in Neurology, 18: pp 504-510 (2005) McClorey, G.P., Fletcher, S. and Wilton, S.D. Splicing intervention for Duchenne muscular dystrophy, Current Opinion in Pharmacology, 5: pp 529-534 (2005) Meloni, B.P., Van Dyk, D., Cole, R. and Knuckey, N.W. Proteome analysis of cortical neuronal cultures following cycloheximide, heat street and MK801 preconditioning, Proteomics, 5: pp 4743-4753 (2005) Rodrigues, J.P.T., Edwards, D.J., Walters, S.E., Byrnes, M.L., Thickbroom, G.W., Stell, R. and Mastaglia, F.L. Gabapentin can improve postural stability and quality of life in primary orthostatic tremor, Movement Disorders, 20:7, pp 865-870 (2005) Thickbroom, G.W., Byrnes, M.L., Archer, S.R., Kermode, A.G. and Mastaglia, F.L. Corticomotor organisation and motor function in multiple sclerosis, Journal of Neurology, 252: pp 765-771 (2005) Williams, D.R., Reardon, K., Roberts, L., Dennet, X., Duff, R., Laing, N.G. and Byrne, E. A new dominant distal myopathy affecting posterior leg and anterior upper limb muscles, Neurology, 64: pp 1245-1254 (2005) Wilton, S.D. and Fletcher, S. RNA splicing manipulation: strategies to modify gene expression for a variety of therapeutic outcomes, Current Gene Therapy, 5: pp 467-483 (2005) Wilton, S.D. and Fletcher, S. Antisense oligonucleotides in the treatment of Duchenne muscular dystrophy: Where are we now?, Neuromuscular Disorders, 15: pp 399-402 (2005) Zhu, H., Meloni, B.P., Bojarski, C., Knuckey, M.W. and Knuckey, N.W. Post-ischaemic modest hypothermia (35o C) combined with intravenous magnesium is more effective at reducing CA1 neuronal death than either treatment used alone following global cerebral ischemia in rats, Experimental Neurology, 193: pp 361-368 (2005) Conference PublicationsLee, V., Bolitho, E., Mastaglia, F.L. and Garlepp, M. Dopamine Receptor D2 (DRD2) and COMT polymorphisms in Parkinson's Disease, 7th International Congress on Alzheimer's Disease and Parkinson's Disease, Italy, Medimond S.R.L., 1: pp 197-201 (2005) Mastaglia, F.L., Bolitho, E., Van Bockxmeer, F. and Garlepp, M. Glutathione S-Transferase P1 (GSTP1) and Apolipoprotein E (APOE) Gene Polymorphisms in Parkisnon's Disease, 7th International Congress on Alzheimer's Disease and Parkinson's Disease, Italy, Medimond S.R.L., 1: pp 191-195 (2005) |