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Showing articles 0 to 15 of 15 Filter Applied: myopathy (Click to remove) Telemedicine in Neurology Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020 Teleneurology Pract Neurol 19:13, Gollomp, S. & Mathew, P.G., 2020 Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes) NEJM 376:1668-1678, CASE 13-2017, 2017 The Myositis Autoantibody Phenotypes of the Juvenile Idiopathic Inflammatory Myopathies Medicine 92:223-243, Rider, L.,et al, 2013 An Unusual Cause of Symptomatic Tension-Type Headache: Hypertrophic Branchial Myopathy Neurol 76:488, Desestret,V.,et al, 2011 Mitochondrial DNA Polymerase-y and Human Disease Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006 Neurologic Aspects of Inflammatory Bowel Disease Neurol 45:416-421, Lossos,A.,et al, 1995 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Neuromuscular Manifestations of Wegener's Granulomatosis:A Case Report Neurol 43:617-618, Finkelman,R.,et al, 1993 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation Neurol 42:545-550, Goto,Y.,et al, 1992 Dystrophinopathy in Isolated Cases of Myopathy in Females Neurol 42:967-975, Hoffman,E.P.,et al, 1992 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 Sarcoidosis of the Nervous System, A Clinical Approach Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991 MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission Neurol 38:751-754, Montagne,P.,et al, 1988 Neurologic Manifestations in Sarcoidosis Ann Int Med 87:336, Delaney,P., 1977 Showing articles 0 to 15 of 15