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Journal of Inherited Metabolic Disease|January 1, 1991
Agoraphobia in phenylketonuriaS E Waisbren, H L LevyActa Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
The future of newborn screening belongs to obstetriciansM I Evans, H L LevyThe New England Journal of Medicine|November 20, 1980
Maternal phenylketonuria and hyperphenylalaninemia. An international survey of the outcome of untreated and treated pregnanciesR R Lenke, H L LevyCurrent Opinion in Pediatrics|December 1, 1994
Current approaches to genetic metabolic screening in newbornsH L Levy, A S CornierAmerican Journal of Obstetrics and Gynecology|March 1, 1982
Maternal phenylketonuria--results of dietary therapyR R Lenke, H L LevyThe 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 LevyPediatrics|October 1, 1984
Massachusetts Metabolic Disorders Screening Program: III. SarcosinemiaH L Levy, J T Coulombe, R BenjaminPageof 13