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The American Journal of Clinical Nutrition|March 13, 1998
Tyrosine supplementation in the treatment of maternal phenylketonuriaF J Rohr, D Lobbregt, H L LevyAmerican Journal of Medical Genetics|October 26, 2000
Gomez-Lopez-Hernandez syndrome: expansion of the phenotypeD Brocks, M Irons, A Sadeghi-Najad, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|May 1, 1975
Comparison of galactose-1-phosphate uridyl transferase in fetal and adult tissuesG Hammersen, H L Levy, F Frigoletto, et al.Pediatrics|January 1, 1981
Massachusetts Metabolic Disorders Screening Program. II. Methylmalonic aciduriaJ T Coulombe, V E Shih, H L LevyThe New England Journal of Medicine|November 24, 1999
Reduction of false negative results in screening of newborns for homocystinuriaM J Peterschmitt, J R Simmons, H L LevyJournal of Inherited Metabolic Disease|January 1, 1992
Prenatal diagnosis of non-ketotic hyperglycinaemiaJ R Toone, D A Applegarth, H L LevyMolecular Biology & Medicine|February 1, 1991
Histidase and histidinemia. Clinical and molecular considerationsR G Taylor, H L Levy, R R McInnesThe Journal of Pediatrics|June 1, 1982
Comparison of treated and untreated pregnancies in a mother with phenylketonuriaH L Levy, G N Kaplan, A M EricksonJournal of Inherited Metabolic Disease|May 26, 2004
Maternal histidinaemia: pregnancies and offspring outcomesH L Levy, J J Yu, S E WaisbrenResearch Communications in Chemical Pathology and Pharmacology|February 1, 1989
Homocysteine thiolactone: failure to detect in human serum or plasmaS H Mudd, A I Matorin, H L LevyPageof 15