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

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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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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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Neuromuscular disease and respiratory failure von Hutchinson, D, Whyte, K

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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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Curve Number Estimation Accuracy on Disturbed and Undisturbed Soils von Christianson, Reid D, Hutchinson, Stacy L, Brown, Glenn O

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Safety and efficacy of gemtuzumab ozogamicin in pediatric patients with advanced CD33+ acute myeloid leukemia von Arceci, Robert J., Sande, Jane, Lange, Beverly, Shannon, Kevin, Franklin, Janet, Hutchinson, Raymond, Vik, Terry A., Flowers, David, Aplenc, Richard, Berger, Mark S., Sherman, Matthew L., Smith, Franklin O., Bernstein, Irwin, Sievers, Eric L.

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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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Bone Plug Versus Suture-Only Fixation of Meniscal Grafts: Effect on Joint Contact Mechanics During Simulated Gait von Wang, Hongsheng, Gee, Albert O., Hutchinson, Ian D., Stoner, Kirsten, Warren, Russell F., Chen, Tony O., Maher, Suzanne A.

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