Showing results (1-10 of 12) with videos related to
Sort By:
Pageof 2
Journal of Inherited Metabolic Disease|November 1, 2002
Elevated plasma phenylalanine concentrations may adversely affect bone status of phenylketonuric miceS Yannicelli, D M MedeirosBiological Trace Element Research|September 1, 1993
Plasma molybdenum concentrations in children with and without phenylketonuriaS S Gropper, S YannicelliBiological Trace Element Research|March 5, 1999
Plasma micronutrient concentrations in infants undergoing therapy for phenylketonuriaP B Acosta, S YannicelliActa Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Protein intake affects phenylalanine requirements and growth of infants with phenylketonuriaP B Acosta, S YannicelliJournal of the American Dietetic Association|February 1, 1994
Nutrition support for glutaric acidemia type IS Yannicelli, F Rohr, M L WarmanJournal of Inherited Metabolic Disease|January 1, 1992
Decreased selenium intake and low plasma selenium concentrations leading to clinical symptoms in a child with propionic acidaemiaS Yannicelli, K M Hambidge, M F PiccianoJournal of Inherited Metabolic Disease|January 1, 1989
Normal growth and development with unrestricted protein intake after severe infantile propionic acidaemiaA S Luder, S Yannicelli, C L GreenJournal of the American College of Nutrition|April 1, 1993
Nutrient intakes of adolescents with phenylketonuria and infants and children with maple syrup urine disease on semisynthetic dietsS S Gropper, M C Naglak, M Nardella, et al.Journal of Inherited Metabolic Disease|January 1, 1989
The management of breast feeding among infants with phenylketonuriaL McCabe, A E Ernest, M R Neifert, et al.Journal of Pediatric Gastroenterology and Nutrition|October 11, 2001
Intake and blood levels of fatty acids in treated patients with phenylketonuriaP B Acosta, S Yannicelli, R Singh, et al.Pageof 2