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Showing articles 0 to 10 of 10 Filter Applied: aminoacidurias (Click to remove) Neurological Deterioration in Young Adults with Phenylketonuria Lancet 336:602-605, Thompson,A.J.,et al, 1990 Cerebral Edema Causing Death in Children with Maple Syrup Urine Disease J Pediatr 119:42-45, Riviello,J.J.,et al, 1991 CNS Lesions in Cystinuria Arch Neurol 34:638, Blackburn,C.R.B.,et al, 1977 Inherited Metabolic Diseases of the Nervous System, Maple Syrup Urine Disease Adams & Victors Principles of Neurology, Chp 37, pg 953, Ropper, A.H.,et al, 2014 Inherited Metabolic Diseases of the Nervous System, The Phenylketonuria Adams & Victors Principles of Neurology, Chp 37, pg 968, Ropper, A.H.,et al, 2014 Diffusion-Weighted Imaging and Proton MR Spectroscopy of White Matter Abnormalities in a Case of Phenylketonuria Eur J Radiol Extra 54: 5-9, Teksam,M.,et al., 2005 Ophthalmoplegia & Bulbar Palsy in Variant Form of Maple Syrup Urine Disease Ann Neurol 6:71-72, Chhabria,S.,et al, 1979 Diagnosis of Treatable Wilson's Disease NEJM 298:1347, Cartwright,G.E., 1978 Free Amino Acid Levels in Amyotrophic Lateral Sclerosis Ann Neurol 3:305, Patten,B.M.,et al, 1978 A Synd of Methylmal Acid, Homocystinuria, Megaloblas. Anemia & Neurol Abnor. in a Vit B-12-def Breast-fed Infant of veget NEJM 299:317, Higginbottom,M.C., 1978 Showing articles 0 to 10 of 10