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Pediatrics|June 5, 2001
Detection of neonatal carnitine palmitoyltransferase II deficiency by expanded newborn screening with tandem mass spectrometryS Albers, D Marsden, E Quackenbush, et al.
Pediatric Clinics of North America|October 1, 1993
Screening for metabolic disorders. How are we doing?M Irons
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.
Enzyme|January 1, 1987
Maternal phenylketonuria. Review with emphasis on pathogenesisH L Levy
Journal of the American College of Nutrition|January 1, 1989
Nutritional therapy for selected inborn errors of metabolismH L Levy
The Turkish Journal of Pediatrics|July 1, 1996
Reproductive effects of maternal metabolic disorders: implications for pediatrics and obstetricsH L Levy
Current Opinion in Pediatrics|December 1, 1995
Abnormal cholesterol metabolism in Smith-Lemli-Opitz syndromeE R Elias, M Irons
Teratology|March 1, 1996
Maternal phenylketonuria: a metabolic teratogenH L Levy, M Ghavami
Annual Review of Genomics and Human Genetics|November 10, 2001
Genetic screening of newbornsH L Levy, S Albers
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1977
Starch gel electrophoresis for galactose-1-phosphate uridylyl-transferase applied to dried filter paper blood specimensG Hammersen, H L Levy
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