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Journal of the American Dietetic Association|December 28, 1999
Necessity of complete intake of phenylalanine-free amino acid mixture for metabolic control of phenylketonuriaG P Duran, F J Rohr, A Slonim, et al.Radiology|November 1, 1990
Phenylketonuria: MR imaging of the brain with clinical correlationK D Pearsen, A D Gean-Marton, H L Levy, et al.American Journal of Diseases of Children (1960)|November 1, 1993
The North American Collaborative Study of Maternal Phenylketonuria. Status report 1993R Koch, H L Levy, R Matalon, et al.Metabolism: Clinical and Experimental|August 23, 2000
Methionine transamination in patients with homocystinuria due to cystathionine beta-synthase deficiencyA Tangerman, B Wilcken, H L Levy, et al.The New England Journal of Medicine|October 18, 1984
Benign methylmalonic aciduriaF D Ledley, H L Levy, V E Shih, et al.Journal of Child Neurology|November 26, 1999
Atypical nonketotic hyperglycinemia with normal cerebrospinal fluid to plasma glycine ratioA H Jackson, D A Applegarth, J R Toone, et al.Journal of Neuropathology and Experimental Neurology|July 1, 1996
Evidence for central nervous system glial cell plasticity in phenylketonuriaC A Dyer, A Kendler, T Philibotte, et al.Pediatrics|June 5, 2001
Detection of neonatal carnitine palmitoyltransferase II deficiency by expanded newborn screening with tandem mass spectrometryS Albers, D Marsden, E Quackenbush, et al.American Journal of Human Genetics|March 1, 1997
Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A geneM E Chamberlin, T Ubagai, S H Mudd, et al.Bioresource Technology|August 20, 2010
Application of a novel method for optimization of bioemulsan production in a miniaturized bioreactorGh Amoabediny, M Rezvani, H Rashedi, et al.Pageof 14