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Pediatric Pathology|November 1, 1994
Phrenic nerve involvement in Déjérine-Sottas disease: a clinicopathological case studyK J Felice, J D Fratkin, E L Feldman, et al.Neurology|May 24, 2000
FSH dystrophy 4q35 deletion in patients presenting with facial-sparing scapular myopathyK J Felice, W A North, S A Moore, et al.American Journal of Human Genetics|August 12, 1999
Congenital end-plate acetylcholinesterase deficiency caused by a nonsense mutation and an A-->G splice-donor-site mutation at position +3 of the collagenlike-tail-subunit gene (COLQ): how does G at position +3 result in aberrant splicing?K Ohno, J M Brengman, K J Felice, et al.Neurology|July 26, 2000
Autosomal dominant Emery-Dreifuss dystrophy due to mutations in rod domain of the lamin A/C geneK J Felice, R C Schwartz, C A Brown, et al.Neuromuscular Disorders : NMD|April 30, 1999
Autosomal dominant distal myopathy not linked to the known distal myopathy lociK J Felice, C Meredith, N Binz, et al.Neurology|April 10, 2002
A pilot randomized trial of oxandrolone in inclusion body myositisS B Rutkove, R A Parker, R A Nardin, et al.Neurology|November 4, 2000
Adult-onset MLD: a gene mutation with isolated polyneuropathyK J Felice, M Gomez Lira, M Natowicz, et al.Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|November 1, 1995
Methods for estimating the numbers of motor units in human musclesT Doherty, Z Simmons, B O'Connell, et al.Neurology|December 31, 1997
Effect of recombinant human insulin-like growth factor-I on progression of ALS. A placebo-controlled study. The North America ALS/IGF-I Study GroupE C Lai, K J Felice, B W Festoff, et al.Neurology|August 27, 2003
A randomized, placebo-controlled trial of topiramate in amyotrophic lateral sclerosisM E Cudkowicz, J M Shefner, D A Schoenfeld, et al.Pageof 3