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Neurology|October 16, 1999
Clinical and therapeutic observations in aromatic L-amino acid decarboxylase deficiencyK J Swoboda, K Hyland, D S Goldstein, et al.
Prenatal Diagnosis|July 1, 1986
Prenatal diagnosis of non-ketotic hyperglycinemiaD A Applegarth, H L Levy, V E Shih, et al.
The Journal of Pediatrics|January 1, 1987
Folinic acid therapy in treatment of dihydropteridine reductase deficiencyM Irons, H L Levy, M E O'Flynn, et al.
American Journal of Obstetrics and Gynecology|April 1, 1992
Maternal phenylketonuria collaborative study, obstetric aspects and outcome: the first 6 yearsL D Platt, R Koch, C Azen, et al.
American Journal of Human Genetics|October 1, 1995
Isolated persistent hypermethioninemiaS H Mudd, H L Levy, A Tangerman, et al.
The Journal of Pediatrics|January 1, 1990
Partial biotinidase deficiency: clinical and biochemical featuresJ R McVoy, H L Levy, M Lawler, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
The international collaborative study of maternal phenylketonuria: status report 1994R Koch, H L Levy, R Matalon, et al.
European Journal of Pediatrics|July 1, 1996
Maternal non-phenylketonuric mild hyperphenylalaninemiaH L Levy, S E Waisbren, D Lobbregt, et al.
American Journal of Human Genetics|July 1, 1995
A missense mutation (I278T) in the cystathionine beta-synthase gene prevalent in pyridoxine-responsive homocystinuria and associated with mild clinical phenotypeV E Shih, J M Fringer, R Mandell, et al.
American Journal of Human Genetics|March 21, 2000
Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variationsM E Chamberlin, T Ubagai, S H Mudd, et al.
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