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Showing articles 0 to 9 of 9 Filter Applied: ataxia (Click to remove) Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes) NEJM 376:1668-1678, CASE 13-2017, 2017 Heterogeneity of Coenzyme Q10 Deficiency Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012 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 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis Ann Neurol 18:614-617, Wolf,B.,et al, 1985 Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin NEJM 304:817-820, Thoene,J.,et al, 1981 Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981 Adult Toxoplasmosis Presenting as Polymyositis & Cerebellar Ataxia Ann Int Med 82:367, Greenlee,J.,et al, 1975 Showing articles 0 to 9 of 9