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Showing articles 0 to 15 of 15 Filter Applied: genetic testing (Click to remove) MELAS Presenting as Bilateral Symmetric Occipital and Temporal Cortices Lesions, A Case Report and Literature Review Neurologist 30:75-79, Liu,Q.,et al, 2025 Melas Syndrome Stat PearlsPubl Jan 25, Pia,S. & Lui,F., 2025 "Disappearing Infarct" Is Late-Onset MELAS Ann Neurol 90:1001-1002, Landis,T.M.,et al, 2021 Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy NEJM 381:164-172, Case 21-2019, 2019 Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes) NEJM 376:1668-1678, CASE 13-2017, 2017 A 10-year-old boy with Bilateral Vision Loss Neurol 88:e221-e224, Bulwa, Z.,et al, 2017 Clinical Reasoning: Encephalopathy in a 10-year-old boy Neurol 79:e12-e18, Rodan, L. & Tein, I., 2012 Wolff-Parkinson-White Syndrome in Patients with MELAS Arch Neurol 64:1625-1627, Sproule,D.M.,et al, 2007 Metabolic Disease and Stroke: MELAS emedicine.com, Mandava,P.,et al, 2006 Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects Lancet Neurol 4:239-248, Shahwan, A., et al, 2005 The Polymerase Chain Reaction:Application to Nervous System Disease Ann Neurol 34:513-523, Darnell,R.B., 1993 A 67-Year-Old Man with Exercise Intolerance nd Progressive Weakness Neurol 106:e214830, Gosset,A.,et al, 2026 A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis Neurol 103:e209708, Wannarong,T.,et al, 2024 Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023 FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018 Showing articles 0 to 15 of 15