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Muscle & Nerve|June 18, 2009
Serum creatine kinase levels in spinobulbar muscular atrophy and amyotrophic lateral sclerosisNizar Chahin, Eric J SorensonNeurology|September 21, 2007
Correlation of muscle biopsy, clinical course, and outcome in PM and sporadic IBMNizar Chahin, Andrew G EngelNeurology(R) Neuroimmunology & Neuroinflammation|January 31, 2015
Toxoplasmic encephalitis during mycophenolate mofetil immunotherapy of neuromuscular diseaseDanilo R Bernardo, Nizar ChahinMuscle & Nerve|January 13, 2026
Expanding the Differential Diagnosis of Ultrasonographic Flexor Digitorum Profundus-Flexor Carpi Ulnaris Dissociation of Echogenicity: Muscular DystrophiesAnson W Wilks, Nizar ChahinNeurology|September 9, 2005
Sporadic late onset nemaline myopathyNizar Chahin, Duygu Selcen, Andrew G EngelJournal of Neurology|July 1, 2019
Bright tongue sign in patients with late-onset Pompe diseaseChafic Karam, Diana Dimitrova, Elizabeth Yutan, et al.Neurology|May 21, 2008
Natural history of spinal-bulbar muscular atrophyNizar Chahin, Christopher Klein, Jayawant Mandrekar, et al.Muscle & Nerve|July 17, 2015
Late-onset Becker muscular dystrophy: Refining the clinical features and electrophysiological findingsTania Beltran Papsdorf, James F Howard, Nizar ChahinJournal of Neurology|May 14, 2020
Screening for genetic mutations in patients with neuropathy without definite etiology is usefulBraden Vogt, Nizar Chahin, Wojciech Wiszniewski, et al.Arthritis Care & Research|July 26, 2024
Benefits of Early Versus Late Initiation of Intravenous Immunoglobulin in the Treatment of Patients With Anti-3-Hydroxy-3-Methylglutaryl-Coenzyme A Reductase Immune-Mediated Necrotizing MyopathyKyle Sharf, Toan Do, Daniela Ghetie, et al.Pageof 3