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The Journal of Pediatrics|July 1, 1975
Rennes-like variant of galactosemia: clinical and biochemical studiesG Hammersen, S Houghton, H L LevyArchives of Disease in Childhood|August 1, 1975
Asymptomatic type II hyperprolinaemia associated with hyperglycinaemia in three sibsL Pavone, F Mollica, H L LevyThe Journal of Laboratory and Clinical Medicine|June 1, 1982
A new method of screening for inherited disorders of galactose metabolismK Paigen, F Pacholec, H L LevyAnnals of Human Genetics|October 1, 1975
Galactose-1-phosphate uridyl transferase in fibroblasts: isozymes in normal and variant statesG Hammersen, R Mandell, H L LevyRadiology|March 1, 1989
Amyloidosis: diffuse involvement of the retroperitoneumT P Glynn, D L Kreipke, J M IronsPediatrics|October 1, 1984
Massachusetts Metabolic Disorders Screening Program: III. SarcosinemiaH L Levy, J T Coulombe, R BenjaminAnnals of Neurology|September 1, 1986
Bilateral lucency of the globus pallidus complicating methylmalonic acidemiaB Korf, J K Wallman, H L LevyClinical Obstetrics and Gynecology|September 1, 1986
Prevention of fetal damage through dietary control of maternal hyperphenylalaninemiaM Ghavami, H L Levy, R W ErbeJournal 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 LevyThe Journal of Primary Prevention|November 23, 2013
A psychosocial model of a medical problem: Maternal phenylketonuriaS Shiloh, S E Waisbren, H L LevyPageof 15