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Showing articles 0 to 8 of 8 Filter Applied: histochemistry of muscle (Click to remove) A 64-year-old Man with Progressive Paraspinal Muscle Weakness Neurol 86:e4-e9, Schneider, R.,et al, 2016 Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form Neurol 46:815-818, Kobayashi,O.,et al, 1996 Cytochrome c Oxidase Deficiency in Leigh Syndrome Ann Neurol 22:498-506, DiMauro,S.,et al, 1987 Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining Neurol 46:810-814, Connolly,A.M.,et al, 1996 Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996 Erroneous Diagnosis Corrected After 28 Years Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996 Late Denervation in Patients with Antecedent Paralytic Poliomyelitis NEJM 317:7-12, Cashman,N.R.,et al, 1987 Congenital Myotonic Dystrophy Arch Neurol 37:693-696, Argov,Z.,et al, 1980 Showing articles 0 to 8 of 8