Showing results (11-20 of 100) with videos related to
Sort By:
Pageof 10
Journal 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 BerryBiomedical Mass Spectrometry|December 1, 1979
Identification and quantitation of urinary dicarboxylic acids as their dicyclohexyl esters in disease states by gas chromatography mass spectrometryE J Norman, H K Berry, M D DentonClinical Genetics|February 1, 1978
Galactose-1-phosphate accumulation by a Duarte-transferase deficiency double heterozygoteC H Wharton, H K Berry, M K BofingerNeuroscience and Biobehavioral Reviews|January 1, 1981
Progress in experimental phenylketonuria: a critical reviewC V Vorhees, R E Butcher, H K BerryClinical Chemistry|January 1, 1982
Gas-chromatographic/mass spectrometric detection of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency in double first cousinsE J Norman, M D Denton, H K BerryBiology 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.American Journal of Diseases of Children (1960)|October 1, 1980
Elevated meconium lactase activity. Its use as a screening test for cystic fibrosisH K Berry, F W Kellogg, S R Lichstein, et al.American Journal of Diseases of Children (1960)|February 1, 1982
Diagnosis of phenylalanine hydroxylase deficiency (phenylketonuria)H K Berry, M H Hsieh, M K Bofinger, et al.Journal of Chromatography|January 11, 1985
Rapid gas chromatographic--mass spectrometric quantitation of gamma-aminobutyric acid in biological specimensE J Norman, E L Wee, H K Berry, et al.Pageof 10