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Muscle & Nerve|October 15, 1998
Primary alpha-sarcoglycan deficiency responsive to immunosuppression over three yearsA M Connolly, A Pestronk, S Mehta, et al.Current Opinion in Rheumatology|November 7, 1999
Organ-specific autoantibodies with muscle weaknessM Al-Lozi, A PestronkPediatric Neurology|July 31, 1999
Mutation analysis in Emery-Dreifuss muscular dystrophyY Nevo, M Al-Lozi, A S Parsadanian, et al.The Journal of Pediatrics|June 1, 1997
Serum autoantibodies in childhood opsoclonus-myoclonus syndrome: an analysis of antigenic targets in neural tissuesA M Connolly, A Pestronk, S Mehta, et al.Neuromuscular Disorders : NMD|October 12, 2001
Three mouse models of muscular dystrophy: the natural history of strength and fatigue in dystrophin-, dystrophin/utrophin-, and laminin alpha2-deficient miceA M Connolly, R M Keeling, S Mehta, et al.The Journal of Infectious Diseases|December 13, 1997
Anti-tubulin autoantibodies in acquired demyelinating polyneuropathiesA M Connolly, A PestronkNeurology|March 1, 1996
Congenital muscular dystrophy syndromes distinguished by alkaline and acid phosphatase, merosin, and dystrophin stainingA M Connolly, A Pestronk, G J Planer, et al.The Journal of Pediatrics|May 6, 1999
Serum autoantibodies to brain in Landau-Kleffner variant, autism, and other neurologic disordersA M Connolly, M G Chez, A Pestronk, et al.Neurology|August 11, 2010
Dominant spinal muscular atrophy with lower extremity predominance: linkage to 14q32M B Harms, P Allred, R Gardner, et al.Neurology|January 1, 1997
Serum IgM monoclonal autoantibody binding to the 301 to 314 amino acid epitope of beta-tubulin: clinical association with slowly progressive demyelinating polyneuropathyA M Connolly, A Pestronk, S Mehta, et al.Pageof 227