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Neurologic Clinics|October 13, 1999
Creutzfeldt-Jakob disease, new variant creutzfeldt-jakob disease, and bovine spongiform encephalopathyC C Weihl, R P RoosNeuropathology and Applied Neurobiology|January 24, 2017
Sporadic inclusion body myositis - a myodegenerative disease or an inflammatory myopathyC C Weihl, A L MammenContinuum (Minneapolis, Minn.)|December 20, 2022
Genetic-Based Treatment Strategies for Muscular Dystrophy and Congenital MyopathiesAndrew R Findlay, Conrad C WeihlHuman Molecular Genetics|April 23, 2010
Inclusion body myopathy, Paget's disease of the bone and fronto-temporal dementia: a disorder of autophagyJeong-Sun Ju, Conrad C WeihlAutophagy|February 27, 2013
Rapamycin-induced autophagy aggravates pathology and weakness in a mouse model of VCP-associated myopathyJames K Ching, Conrad C WeihlJournal of the Neurological Sciences|December 23, 2008
Inflammatory myopathies with mitochondrial pathology and protein aggregatesPeyker Temiz, Conrad C Weihl, Alan PestronkGenes|February 25, 2022
Current and Future Approaches to Classify VUSs in LGMD-Related GenesChengcheng Li, Gabe Haller, Conrad C WeihlNeurology|June 16, 2006
Valproate may improve strength and function in patients with type III/IV spinal muscle atrophyConrad C Weihl, Anne M Connolly, Alan PestronkJournal of Virology|September 11, 1999
Alternative translation initiation of Theiler's murine encephalomyelitis virusK Yamasaki, C C Weihl, R P RoosNeuromuscular Disorders : NMD|April 22, 2009
Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementiaConrad C Weihl, Alan Pestronk, Virginia E KimonisPageof 14