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Showing articles 0 to 14 of 14 Filter Applied: histochemistry of muscle (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 A 64-year-old Man with Progressive Paraspinal Muscle Weakness Neurol 86:e4-e9, Schneider, R.,et al, 2016 X-Linked Vacuolated Myopathy:Membrane Attack Complex Depos on Muscle Fiber Membr with Calcium Accumul on Sarcolemma Ann Neurol 41:117-120, Louboutin,J.P.,et al, 1997 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 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 Clinicopath Conf Myopathy Due to Adult Acid Maltase Deficiency, 36-1986, NEJM 315:694-701986., , 1986 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 Adult Onset Nemaline Myopathy Neurol 28:1306-1309, Brownell,A.K.W.,et al, 1978 The Adult Form of Acid Maltase (a-1, 4-Glucosidase) Deficiency Ann Neurol 1:276, Karpati,G.,et al, 1977 Showing articles 0 to 14 of 14