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Annals of Neurology|September 1, 1986
Bilateral lucency of the globus pallidus complicating methylmalonic acidemiaB Korf, J K Wallman, H L Levy
Clinical Obstetrics and Gynecology|September 1, 1986
Prevention of fetal damage through dietary control of maternal hyperphenylalaninemiaM Ghavami, H L Levy, R W Erbe
Journal of Inherited Metabolic Disease|January 1, 1993
The use of gelatin capsules for ingestion of formula in dietary treatment of maternal phenylketonuriaH H Kecskemethy, D Lobbregt, H L Levy
The Journal of Primary Prevention|November 23, 2013
A psychosocial model of a medical problem: Maternal phenylketonuriaS Shiloh, S E Waisbren, H L Levy
The American Journal of Clinical Nutrition|March 13, 1998
Tyrosine supplementation in the treatment of maternal phenylketonuriaF J Rohr, D Lobbregt, H L Levy
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 Levy
The 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 Levy
Journal of Inherited Metabolic Disease|January 1, 1992
Prenatal diagnosis of non-ketotic hyperglycinaemiaJ R Toone, D A Applegarth, H L Levy
Molecular Biology & Medicine|February 1, 1991
Histidase and histidinemia. Clinical and molecular considerationsR G Taylor, H L Levy, R R McInnes
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