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The Italian Journal of Gastroenterology|December 1, 1995
Abnormal cholesterol biosynthesis in the Smith-Lemli-Opitz syndromeG Salen, G S Tint, G Xu, et al.Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Review of neuropsychological functioning in treated phenylketonuria: an information processing approachS E Waisbren, M J Brown, L M de Sonneville, et al.American Journal of Human Genetics|November 1, 1981
A study of cardiovascular risk in heterozygotes for homocystinuriaS H Mudd, R Havlik, H L Levy, et al.Journal of the American Dietetic Association|December 28, 1999
Necessity of complete intake of phenylalanine-free amino acid mixture for metabolic control of phenylketonuriaG P Duran, F J Rohr, A Slonim, et al.Radiology|November 1, 1990
Phenylketonuria: MR imaging of the brain with clinical correlationK D Pearsen, A D Gean-Marton, H L Levy, et al.American Journal of Diseases of Children (1960)|November 1, 1993
The North American Collaborative Study of Maternal Phenylketonuria. Status report 1993R Koch, H L Levy, R Matalon, et al.Metabolism: Clinical and Experimental|August 23, 2000
Methionine transamination in patients with homocystinuria due to cystathionine beta-synthase deficiencyA Tangerman, B Wilcken, H L Levy, et al.The New England Journal of Medicine|October 18, 1984
Benign methylmalonic aciduriaF D Ledley, H L Levy, V E Shih, et al.Journal of Child Neurology|November 26, 1999
Atypical nonketotic hyperglycinemia with normal cerebrospinal fluid to plasma glycine ratioA H Jackson, D A Applegarth, J R Toone, et al.Journal of Neuropathology and Experimental Neurology|July 1, 1996
Evidence for central nervous system glial cell plasticity in phenylketonuriaC A Dyer, A Kendler, T Philibotte, et al.Pageof 15