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Showing articles 0 to 11 of 11 Filter Applied: histochemistry (Click to remove) The Wide Spectrum of Myofibrillar Myopathy Suggests a Multifactorial Etiology and Pathogenesis Neurol 51:1646-1655, Amato,A.A.,et al, 1998 Acute Type II Myofiber Atrophy in Critical Illness Neurol 46:819-821, 6001996., Gutman,L.,et al, 1996 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 Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps NEJM 327:1100, Minetti,C.&Bonilla,E., 1992 Mosaic Expression of Dystrophic in Symptomatic Carriers of Duchenne's Muscular Dystrophy NEJM 320:138-142, Arahata,K.,et al, 1989 Late Denervation in Patients with Antecedent Paralytic Poliomyelitis NEJM 317:7-12, Cashman,N.R.,et al, 1987 Cytochrome c Oxidase Deficiency in Leigh Syndrome Ann Neurol 22:498-506, DiMauro,S.,et al, 1987 Congenital Myotonic Dystrophy Arch Neurol 37:693-696, Argov,Z.,et al, 1980 Acridine Orange-Nucleic Acid Fluorescence Arch Neurol 37:641-644, Perl,D.P.,et al, 1980 Showing articles 0 to 11 of 11