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Current Opinion in Neurology|October 23, 1997
Inclusion body myositis and myopathiesK Sivakumar, M C DalakasNeurology|October 1, 1996
The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps-sparing phenotype in non-Iranian JewsK Sivakumar, M C DalakasCurrent Opinion in Neurology|June 1, 1996
The immunopathologic and inflammatory differences between dermatomyositis, polymyositis and sporadic inclusion body myositisM C Dalakas, K SivakumarBrain : a Journal of Neurology|April 1, 1997
An inflammatory, familial, inclusion body myositis with autoimmune features and a phenotype identical to sporadic inclusion body myositis. Studies in three familiesK Sivakumar, C Semino-Mora, M C DalakasNeurology|May 1, 1996
Late-onset muscle weakness in partial phosphofructokinase deficiency: a unique myopathy with vacuoles, abnormal mitochondria, and absence of the common exon 5/intron 5 junction point mutationK Sivakumar, O Vasconcelos, L Goldfarb, et al.Muscle & Nerve|November 1, 1996
Electrophysiologic and histologic studies in clinically unaffected muscles of patients with prior paralytic poliomyelitisC A Luciano, K Sivakumar, S A Spector, et al.Journal of Neuroimmunology|June 17, 1998
HLA allele distribution distinguishes sporadic inclusion body myositis from hereditary inclusion body myopathiesB M Koffman, K Sivakumar, T Simonis, et al.Neurology|March 1, 1997
Treatment of inclusion-body myositis with IVIg: a double-blind, placebo-controlled studyM C Dalakas, B Sonies, J Dambrosia, et al.Neurology|February 15, 2001
A controlled study of intravenous immunoglobulin combined with prednisone in the treatment of IBMM C Dalakas, B Koffman, M Fujii, et al.Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|March 1, 1996
Coexistence of diabetes and phosphofructokinase deficiencyS I Rubio, K K Naha, K Sivakumar, et al.Pageof 33