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Muscle & Nerve|August 25, 2006
Motor neuron disease associated with copper deficiencyConrad C Weihl, Glenn LopateJournal 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.Neuromuscular Disorders : NMD|January 6, 2015
Autophagic vacuolar pathology in desminopathiesConrad C Weihl, Stanley Iyadurai, Robert H Baloh, et al.Continuum (Minneapolis, Minn.)|December 4, 2019
Sporadic Inclusion Body Myositis and Other Rimmed Vacuolar MyopathiesConrad C WeihlNeurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|February 15, 2013
Monitoring autophagy in the treatment of protein aggregate diseases: steps toward identifying autophagic biomarkersConrad C WeihlThe Journal of Clinical Investigation|November 23, 2011
Another VCP interactor: NF is enoughConrad C WeihlAnnals of Neurology|February 16, 2012
Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathyMatthew B Harms, R Brian Sommerville, Peggy Allred, et al.Autophagy|August 17, 2017
Regulation of SQSTM1/p62 via UBA domain ubiquitination and its role in diseaseYouJin Lee, Conrad C WeihlAutophagy|October 11, 2021
Loss-of-function mutation in VCP mimics the characteristic pathology as in FTLD-TARDBPAbubakar Wani, Conrad C WeihlCurrent Opinion in Neurology|June 9, 2025
Myofibrillar myopathy: towards a mechanism-based definition as a Z-disk-opathyMichio Inoue, Conrad C WeihlPageof 14