Autonomic dysfunction is a major feature of cerebellar ataxia, neuropathy, vestibular areflexia 'CANVAS' syndrome von WU, Teddy Y, TAYLOR, Jennifer M, ANDERSON, Neil E, SNOW, Barry J, ANDERSON, Tim J, PAERMENTIER, Laura A. F, CUTFIELD, Nick J, CHANCELLOR, Andrew M, MOSSMAN, Stuart S, ROXBURGH, Richard H, KILFOYLE, Dean H, SMITH, Andrew D, MCGUINNESS, Ben J, SIMPSON, Mark P, WALKER, Elizabeth B, BERGIN, Peter S, CLELAND, James C, HUTCHINSON, David O

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Clinical and laboratory features of patients with myophosphorylase deficiency (McArdle disease) von Miteff, F, Potter, H.C, Allen, J, Teoh, H, Roxburgh, R, Hutchinson, D.O

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A novel ryanodine receptor mutation and genotype-phenotype correlation in a large malignant hyperthermia New Zealand Maori pedigree von BROWN, R. L, POLLOCK, A. N, COUCHMAN, K. G, HODGES, M, HUTCHINSON, D. O, WAAKA, R, LYNCH, P, MCCARTHY, T. V, STOWELL, K. M

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Congenital Myasthenic Syndrome Caused by Prolonged Acetylcholine Receptor Channel Openings Due to a Mutation in the M2 Domain of the ε Subunit von Ohno, Kinji, Hutchinson, David O., Milone, Margherita, Brengman, Joan M., Bouzat, Cecilia, Sine, Steven M., Engel, Andrew G.

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New Mutations in Acetylcholine Receptor Subunit Genes Reveal Heterogeneity in the Slow-Channel Congenital Myasthenic Syndrome von Engel, Andrew G., Ohno, Kinji, Milone, Margherita, Wang, Hai-Long, Nakano, Satoshi, Bouzat, Cecilia, Pruitt, J. Ned, Hutchinson, David O., Brengman, Joan M., Bren, Nina, Sieb, Joern P., Sine, Steven M.

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Bilateral brachial plexopathy following laparoscopic bariatric surgery von BRUNETTE, K. E. J, HUTCHINSON, D. O, ISMAIL, H

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Inclusion body myositis : Abnormal protein accumulation does not trigger apoptosis von HUTCHINSON, D. O

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Two-dimensional gel electrophoresis in inclusion body myositis von Hutchinson, D.O, Jongbloed, B

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Intestinal pseudo-obstruction, myasthenia gravis, and thymoma von ANDERSON, N. E, HUTCHINSON, D. O, NICHOLSON, G. I, AITCHESON, F, NIXON, J. M

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Subacute measles encephalitis in an immunocompetent adult von Croxson, M.C., Anderson, N.E., Vaughan, A.A., Hutchinson, D.O., Schroeder, B.A., Cluroe, A.D., Hyatt, A.D.

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Presentation of intravascular lymphomatosis as lumbosacral polyradiculopathy von Viali, Satu, Hutchinson, David O., Hawkins, Timothy E., Croxson, Margaret C., Thomas, Mark, Allen, Jonathan P., Thomas, Stephen M., Powell, Kevin H.

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Limb girdle muscular dystrophy: use of dHPLC and direct sequencing to detect sarcoglycan gene mutations in a New Zealand cohort von HEDGE, M. R, WU, F, CHONG, B, CHIN, E. L. H, HUTCHINSON, D. O, RICHARDS, C. S, KHADILKAR, S, LOVE, D. R

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Myasthenic Syndromes Attributed to Mutations Affecting the Epsilon Subunit of the Acetylcholine Receptor von ENGEL, A. G., HUTCHINSON, D. O., NAKANO, S., MURPHY, L., GRIGGS, R. C., GU, Y., HALL, Z. W., LINDSTROM, J.

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The Spectrum of Congenital End-plate Acetylcholinesterase Deficiency von HUTCHINSON, D. O., ENGEL, A. G., WALLS, T. J., NAKANO, S., CAMP, S., TAYLOR, P., HARPER, C. M., BRENGMAN, J. M.

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Patch-clamp analysis of the properties of acetylcholine receptor channels at the normal human endplate von Milone, Margherita, Hutchinson, David O., Engel, Andrew G.

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Ophthalmoplegic migraine with bilateral involvement von Hutchinson, D O, Donaldson, I M

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Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: Clinical and pathological variability within a kindred von Hutchinson, David O., Charlton, Amanda, Laing, Nigel G., Ilkovski, Biljana, North, Kathryn N.

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G.P.46 Screening for deletion and duplication mutations in genes implicated in LGMD von Roxburgh, R.H, Marquis-Nicholson, R, Hutchinson, D.O, Waddell, L.B, Clarke, N.F, North, K.N, Love, D.R

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Congenital endplate acetylcholinesterase deficiency von HUTCHINSON, D. O, WALLS, T. J, NAKANO, S, CAMP, S, TAYLOR, P, HARPER, C. M, GROOVER, R. V, PETERSON, H. A, JAMIESON, D. G, ENGEL, A. G

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A comparison between electroencephalography and somatosensory evoked potentials for outcome prediction following severe head injury von Hutchinson, D.O., Frith, R.W., Shaw, N.A., Judson, J.A., Cant, B.R.

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