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Biology of the Neonate|January 1, 1975
Serum amino acid concentrations during pregnancy of women heterozygous for phenylketonuriaH K Berry, I B Poncet, B S Sutherland, et al.Biology of the Neonate|January 1, 1975
Biochemical effects of induced phenylketonuria in ratsI B Poncet, H K Berry, R E Butcher, et al.Clinical Biochemistry|October 1, 1987
Screening for mucopolysaccharide disorders with the Berry spot testH K BerryHealth Laboratory Science|July 1, 1977
Screening for metabolic disorders among high risk infants and childrenH K BerryThe Journal of Experimental Zoology|May 1, 1979
Distribution of phenylalanine hydroxylase (EC 1.14.3.1) in liver and kidney of vertebratesM C Hsieh, H K BerryPediatric Research|June 1, 1989
Branched chain amino acids improve complex maze learning in rat offspring prenatally exposed to hyperphenylalaninemia: implications for maternal phenylketonuriaC V Vorhees, H K BerryDigestive Diseases and Sciences|March 1, 1988
Protease inhibitor and defective proteolysis in cystic fibrosisM C Hsieh, H K BerryThe Journal of Pediatrics|June 1, 1983
Early-treated phenylketonuria: neuropsychologic consequencesR L Brunner, M K Jordan, H K BerryJournal of the American Dietetic Association|October 1, 1985
Phenylketonuria, adolescence, and dietM M Hunt, H K Berry, P P WhiteJournal of Inherited Metabolic Disease|January 1, 1987
Phenylketonuria revisited: treatment of adults with behavioural manifestationsR L Brunner, E H Brown, H K BerryPageof 3