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Showing articles 0 to 11 of 11 Filter Applied: enzyme,defect (Click to remove) Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency Neurol 60:1413-1417, Pearl,P.L.,et al, 2003 A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy JAMA Neurol 81:83-84, Hua,L.,et al, 2024 Inherited Metabolic Diseases of the Nervous System, Inherited Hypeammonemia Adams & Victors Principles of Neurology, Chp 37, pg 952, Ropper, A.H.,et al, 2014 Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease Adams & Victors Principles of Neurology, Chp 37, pg 957, Ropper, A.H.,et al, 2014 Clinicopath Conf, Infantile Krabbe Disease NEJM 362:346-356, Case 3-2010, 2010 Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome NEJM 348:33-40, Hayflick,S.J.,et al, 2003 Coma in a Young Anorexic Woman Lancet 357:1944, Blans,M.J.,et al, 2001 Postpartum Coma and Death Due to Carbamoyl-Phosphate Synthetase I Deficiency Ann Int Med 120:216-217, Wong,L-J.C.,et al, 1994 Psychiatric Disturbances in Metachromatic Leukodystrophy Arch Neurol 49:401-406, Hyde,T.M.,et al, 1992 Acute Profound Dystonia in Infants with Glutaric Acidemia Pediatrics 83:228-234, Bergman,I.,et al, 1989 Glycine Encephalopathy NEJM 298:687, Ch'ien,L.T., 1978 Showing articles 0 to 11 of 11