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Showing articles 0 to 9 of 9 Filter Applied: electron microscopy (Click to remove) Cytochrome c Oxidase Deficiency in Leigh Syndrome Ann Neurol 22:498-506, DiMauro,S.,et al, 1987 Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum Ann Neurol 97:611-628, Coppens,S.,et al, 2025 Rabies Encephalomyelitis Arch Neurol 62:873-882,855, Burton,E.C.,et al, 2005 Neurological Presentation of Fabry's Disease in a 52 Year Old Man JNNP 73:340-342, Mohanraj,R.,et al, 2002 The Wide Spectrum of Myofibrillar Myopathy Suggests a Multifactorial Etiology and Pathogenesis Neurol 51:1646-1655, Amato,A.A.,et al, 1998 Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy NEJM 334:362-366, Fadic,R.,et al, 1996 Inclusion Body Myositis, Observations in 40 Patients Brain 112:727-747, Lotz,B.P.,et al, 1989 Acid Maltase Deficiency Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986 Alcoholic Myopathy in Heart & Skeletal Muscle NEJM 301:28-33, Rubin,E., 1979 Showing articles 0 to 9 of 9