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The American Journal of Clinical Nutrition|April 1, 1976
Treatment of children with phenylketonuria using a phenylalanine-free protein hydrolysate (Albumaid XP)H K Berry, B S Sutherland, M M Hunt, et al.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.Journal of the American Dietetic Association|October 1, 1985
Phenylketonuria, adolescence, and dietM M Hunt, H K Berry, P P WhiteAmerican Journal of Diseases of Children (1960)|May 1, 1990
Valine, isoleucine, and leucine. A new treatment for phenylketonuriaH K Berry, R L Brunner, M M Hunt, et al.Developmental Medicine and Child Neurology|February 1, 1985
Preliminary support for the oral administration of valine, isoleucine and leucine for phenylketonuriaM K Jordan, R L Brunner, M M Hunt, et al.The Journal of Pediatrics|March 1, 1994
Early-treated phenylketonuria: adult neuropsychologic outcomeM D Ris, S E Williams, M M Hunt, et al.Pediatric Research|September 1, 1982
Reduction of cerebrospinal fluid phenylalanine after oral administration of valine, isoleucine, and leucineH K Berry, M K Bofinger, M M Hunt, et al.American Journal of Diseases of Children (1960)|February 1, 1975
Dietary supplement and nutrition in children with cystic fibrosisH K Berry, F W Kellogg, M M Hunt, et al.Journal of Inherited Metabolic Disease|August 1, 1997
Adult psychosocial outcome in early-treated phenylketonuriaM D Ris, A M Weber, M M Hunt, et al.Clinical Genetics|June 1, 1983
Comparative diagnostic value of phenylalanine challenge and phenylalanine hydroxylase activity in phenylketonuriaM C Hsieh, H K Berry, M K Bofinger, et al.Pageof 5