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Showing articles 0 to 8 of 8 Filter Applied: enzyme,defect (Click to remove) Abnormality of a Thiamine-Requiring Enzyme in Patients with Wernicke-Korsakoff Syndrome NEJM 297:1367, Blass,J.P.,et al, 1977 Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency NEJM 375:1879-1890, Case 34-2016, 2016 Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome NEJM 348:33-40, Hayflick,S.J.,et al, 2003 Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency Neurol 60:1413-1417, Pearl,P.L.,et al, 2003 Inborn Errors of Urea Synthesis Ann Neurol 35:133-141, Batshaw,M.L., 1994 Brain Imaging in Late-Onset CM2 Gangliosidosis Neurol 43:2055-2058, Streifler,J.Y.,et al, 1993 Psychiatric Disturbances in Metachromatic Leukodystrophy Arch Neurol 49:401-406, Hyde,T.M.,et al, 1992 Reduction of Angiotensin-Converting Enzyme in Substantia Nigra in Early-Onset Schizophrenia NEJM 300:502-503, Arregui,A.,et al, 1979 Showing articles 0 to 8 of 8