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Showing articles 0 to 9 of 9 Filter Applied: aminoacidurias (Click to remove) Clinical & Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Ref to Growth & Renal Function NEJM 324:1318-1325, Charnas,L.R.,et al, 1991 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 Neurological Deterioration in Young Adults with Phenylketonuria Lancet 336:602-605, Thompson,A.J.,et al, 1990 Ultrastructural, Neurological, & Glycosaminoglycan Abnormalities in Lowe's Syndrome Ann Neurol 16:40-49, Wisniewski,K.E.,et al, 1984 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 Glycine Encephalopathy NEJM 298:687, Ch'ien,L.T., 1978 CNS Lesions in Cystinuria Arch Neurol 34:638, Blackburn,C.R.B.,et al, 1977 Pediatric Neurology Psych Annals 2:1, , 1972 Showing articles 0 to 9 of 9