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Showing articles 0 to 6 of 6 Filter Applied: histochemistry of muscle (Click to remove) Cytochrome c Oxidase Deficiency in Leigh Syndrome Ann Neurol 22:498-506, DiMauro,S.,et al, 1987 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 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 Congenital Myotonic Dystrophy Arch Neurol 37:693-696, Argov,Z.,et al, 1980 The Adult Form of Acid Maltase (a-1, 4-Glucosidase) Deficiency Ann Neurol 1:276, Karpati,G.,et al, 1977 Showing articles 0 to 6 of 6