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The New England Journal of Medicine|May 15, 1986
Molecular analysis of the inheritance of phenylketonuria and mild hyperphenylalaninemia in families with both disordersF D Ledley, H L Levy, S L WooJournal of Inherited Metabolic Disease|January 1, 1980
Diet termination in children with phenylketonuria: a review of psychological assessments used to determine outcomeS E Waisbren, R R Schnell, H L LevyNeurology|May 1, 1989
Late onset of distinct neurologic syndromes in galactosemic siblingsJ H Friedman, H L Levy, R M BoustanyBiochemistry|June 23, 1992
Molecular characterization of two galactosemia mutations and one polymorphism: implications for structure-function analysis of human galactose-1-phosphate uridyltransferaseJ K Reichardt, H L Levy, S L WooPediatrics|February 1, 1991
Detection of phenylketonuria in the very early newborn blood specimenL B Doherty, F J Rohr, H L LevyJournal of Inherited Metabolic Disease|January 5, 2002
Acceptability of a new modular protein substitute for the dietary treatment of phenylketonuriaF J Rohr, A W Munier, H L LevyAmerican Journal of Obstetrics and Gynecology|August 1, 1988
The prenatal sonographic diagnosis of lethal multiple pterygium syndrome: a heritable cause of recurrent abortionC Lockwood, M Irons, J Troiani, et al.American Journal of Medical Genetics|November 1, 1992
Comparison of phenylketonuric and nonphenylketonuric sibs from untreated pregnancies in a mother with phenylketonuriaH L Levy, D Lobbregt, C Sansaricq, et al.Journal of Medical Genetics|February 1, 1996
Three prevalent mutations in a patient with phenylalanine hydroxylase deficiency: implications for diagnosis and genetic counsellingP Guldberg, H L Levy, K F Henriksen, et al.Clinical Genetics|May 1, 1975
Free amino acids in extracts of cultured skin fibroblasts from patients with various amino acid metabolic disordersV E Shih, R Mandell, H L Levy, et al.Pageof 15