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Showing articles 0 to 10 of 10 Filter Applied: histochemistry of muscle (Click to remove) Erroneous Diagnosis Corrected After 28 Years Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996 A 64-year-old Man with Progressive Paraspinal Muscle Weakness Neurol 86:e4-e9, Schneider, R.,et al, 2016 Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999 Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form Neurol 46:815-818, Kobayashi,O.,et al, 1996 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 Cytochrome c Oxidase Deficiency in Leigh Syndrome Ann Neurol 22:498-506, DiMauro,S.,et al, 1987 Type I Fiber Atrophy & Internal Nuclei, A Form of Centronuclear Myopathy Arch Neurol 39:520-524, Peyronnard,J-M.,et al, 1982 Extraocular Muscle Biopsy in Chronic Progressive External Ophthalmoplegia Ann Neurol 6:326-339, Ringel,S.P.,et al, 1979 Adult Onset Nemaline Myopathy Neurol 28:1306-1309, Brownell,A.K.W.,et al, 1978 Showing articles 0 to 10 of 10