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Research 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 LevyThe 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 LevyIEEE Transactions on Biomedical Circuits and Systems|July 16, 2013
Wireless sensor networks for monitoring physiological signals of multiple patientsR S Dilmaghani, H Bobarshad, M Ghavami, 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.Pageof 14