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Showing articles 0 to 11 of 11 Filter Applied: ophthalmoplegia,progressive external (Click to remove) Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene Brain 129:1674-1684, Horvath, R.,et al, 2006 Mitochondrial DNA Polymerase-y and Human Disease Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006 Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes) NEJM 376:1668-1678, CASE 13-2017, 2017 Ophthalmologic Manifestations in MELAS Syndrome Arch Neurol 50:977-980, Fang,W.,et al, 1993 Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024 A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis Neurol 103:e209708, Wannarong,T.,et al, 2024 Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009 Erroneous Diagnosis Corrected After 28 Years Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996 Brainstem Encephalitis & The Syndrome Of Miller Fisher Brain 105:481-495, Al-Din,A.N.,et al, 1982 Ophthalmoplegia-Plus Arch Neurol 38:423-426, Okamoto,T.,et al, 1981 Kearns-Sayre Syndrome with Hypoparathyroidism Ann Neurol 3:513, Horwitz,S.J.,et al, 1978 Showing articles 0 to 11 of 11