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Showing articles 0 to 15 of 15 Filter Applied: lactic acidemia (Click to remove) Heterogeneity of Coenzyme Q10 Deficiency Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012 A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review The Neurologist 8:302-312, Thambisetty,M.,et al, 2002 Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999 Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes) NEJM 376:1668-1678, CASE 13-2017, 2017 MELAS MedLink.com, August, Klopstock, T., 2012 A 23-Year-Old Man With Seizures and Visual Deficit Neurol 70:73-78, Boustany,R.-M.,et al, 2008 Mitochondrial Respiratory-Chain Diseases NEJM 348:2656-2668, DiMauro,S. &Schon,E.A., 2003 Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation JNNP 69: 5-12, Gray,R.G.F. et al, 2000 Adult-Onset MELAS Stroke 27:1420-1423, Gilchrist,J.M.,et al, 1996 Ophthalmologic Manifestations in MELAS Syndrome Arch Neurol 50:977-980, Fang,W.,et al, 1993 Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship J Pediatr 115:81-88, Sooth,F.A.,et al, 1989 MELAS Syndrome Involving a Mother & Two Children Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984 Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT Neurol 34:1456-1460, Yamamoto,T.,et al, 1984 Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification Neurol 29:1057-1061, Markesbery,Wm.R., 1979 Showing articles 0 to 15 of 15