Showing results (61-70 of 138) with videos related to
Sort By:
Pageof 14
Journal of Neurology|April 11, 2018
CANOMAD and other chronic ataxic neuropathies with disialosyl antibodies (CANDA)Rocio Garcia-Santibanez, Craig M Zaidman, R Brian Sommerville, et al.Muscle & Nerve|February 3, 2006
Peripheral neuropathy in an outpatient cohort of patients with Sjögren's syndromeGlenn Lopate, Alan Pestronk, Muhammad Al-Lozi, et al.Journal of Neuromuscular Diseases|November 18, 2016
Aceneuramic Acid Extended Release Administration Maintains Upper Limb Muscle Strength in a 48-week Study of Subjects with GNE Myopathy: Results from a Phase 2, Randomized, Controlled StudyZohar Argov, Yoseph Caraco, Heather Lau, et al.Neuromuscular Disorders : NMD|January 6, 2015
Autophagic vacuolar pathology in desminopathiesConrad C Weihl, Stanley Iyadurai, Robert H Baloh, et al.Muscle & Nerve|March 1, 2013
Multifocal radiculoneuropathy during ipilimumab treatment of melanomaGeorgios Manousakis, James Koch, R Brian Sommerville, et al.Annals of Neurology|November 11, 2014
Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genesJanet Cady, Peggy Allred, Taha Bali, et al.Nature Genetics|March 23, 2004
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing proteinGiles D J Watts, Jill Wymer, Margaret J Kovach, et al.Annals of Neurology|February 16, 2012
Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathyMatthew B Harms, R Brian Sommerville, Peggy Allred, et al.JIMD Reports|May 14, 2015
Rhabdomyolysis-Associated Mutations in Human LPIN1 Lead to Loss of Phosphatidic Acid Phosphohydrolase ActivityGeorge G Schweitzer, Sara L Collier, Zhouji Chen, et al.Neuromuscular Disorders : NMD|January 25, 2015
Targeted sequencing and identification of genetic variants in sporadic inclusion body myositisConrad C Weihl, Robert H Baloh, Youjin Lee, et al.Pageof 14