Enter your terms above and click the 'Search' button.

Showing articles 0 to 12 of 12 Filter Applied: aminoacidopathies (Click to remove) Inherited Metabolic Diseases of the Nervous System, Pyridoxine Dependent Seizures Adams & Victors Principles of Neurology, Chp 37, pg 951, Ropper, A.H.,et al, 2014 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 Neurological Findings in Aminoacylase 1 Deficiency Neurol 68:2151-2153, Sass,J.O.,et al, 2007 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 Neurologic Crises in Hereditary Tyrosinemia NEJM 322:432-437, Mitchell,G.,et al, 1990 Biochemical Genetics Of Neurologic Disease NEJM 305:1181-1193, Rosenberg,R.N., 1981 Ophthalmoplegia & Bulbar Palsy in Variant Form of Maple Syrup Urine Disease Ann Neurol 6:71-72, Chhabria,S.,et al, 1979 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 Possible Pathophysiology of Neurologic Abnormalities assoc. with Nonketotic hyperglycinemia NEJM 294:1295, Ramson,B.R., 1976 Inherited Aminoacidopathies Demonstrating Vitamin Dependency NEJM 281:145, Rosenberg,L., 1965 Showing articles 0 to 12 of 12