Enter your terms above and click the 'Search' button.

Showing articles 0 to 9 of 9 Filter Applied: histochemistry of muscle (Click to remove) Extraocular Muscle Biopsy in Chronic Progressive External Ophthalmoplegia Ann Neurol 6:326-339, Ringel,S.P.,et al, 1979 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 Erroneous Diagnosis Corrected After 28 Years Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996 Cytochrome c Oxidase Deficiency in Leigh Syndrome Ann Neurol 22:498-506, DiMauro,S.,et al, 1987 Quadriceps Myopathy:A Varient of the Limb-Girdle Dystrophy Syndrome JNNP 46:355-357, Swash,M.,et al, 1983 Congenital Myotonic Dystrophy Arch Neurol 37:693-696, Argov,Z.,et al, 1980 5'-Nucleotidase Activity in Duchenne Muscular Dystrophy NEJM 301:726, Scholte,H.R.,et al, 1979 Showing articles 0 to 9 of 9