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Muscle & Nerve|January 17, 2012
Clinical utility of sensory nerve conduction of medial femoral cutaneous nerveShin J Oh, Yuki Hatanaka, Masayuki Ohira, et al.Neurologic Clinics|April 16, 2018
Lambert-Eaton Myasthenic SyndromeVita G Kesner, Shin J Oh, Mazen M Dimachkie, et al.Muscle & Nerve|October 30, 2014
Asymptomatic vasculitic neuropathySemiha Kurt, Mohammad Alsharabati, Liang Lu, et al.Muscle & Nerve|July 21, 2018
Deflazacort versus prednisone/prednisolone for maintaining motor function and delaying loss of ambulation: A post HOC analysis from the ACT DMD trialPerry B Shieh, Joseph Mcintosh, Fengbin Jin, et al.Developmental Dynamics : an Official Publication of the American Association of Anatomists|January 24, 2008
Muscleblind-like 2 (Mbnl2) -deficient mice as a model for myotonic dystrophyMinqi Hao, Kevan Akrami, Ke Wei, et al.Neurology|March 3, 2019
Myasthenic congenital myopathy from recessive mutations at a single residue in Na<sub>V</sub>1.4Nathaniel Elia, Johanna Palmio, Marisol Sampedro Castañeda, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 14, 2004
Anti-Hu antibody neuropathy: a clinical, electrophysiological, and pathological studyShin J Oh, Yasar Gürtekin, Edward J Dropcho, et al.Journal of Comparative Effectiveness Research|October 25, 2021
Meta-analyses of deflazacort versus prednisone/prednisolone in patients with nonsense mutation Duchenne muscular dystrophyPerry B Shieh, Gary Elfring, Panayiota Trifillis, et al.Neuromuscular Disorders : NMD|November 2, 2019
Large in-frame 5' deletions in DMD associated with mild Duchenne muscular dystrophy: Two case reports and a review of the literatureElizabeth M Gibbs, Florian Barthélémy, Emilie D Douine, et al.Journal of Comparative Effectiveness Research|February 7, 2023
Disease progression rates in ambulatory Duchenne muscular dystrophy by steroid type, patient age and functional statusCraig M McDonald, Jessica R Marden, Perry B Shieh, et al.Pageof 15