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The Journal of Pediatrics|August 1, 1989
Parenteral nutrition in propionic and methylmalonic acidemiaS G Kahler, D S Millington, S D Cederbaum, et al.American Journal of Human Genetics|August 1, 1986
The gene for human liver arginase (ARG1) is assigned to chromosome band 6q23R S Sparkes, G J Dizikes, I Klisak, et al.American Journal of Medical Genetics|January 8, 1999
Eye findings in 8 children and a spontaneously aborted fetus with RSH/Smith-Lemli-Opitz syndromeL O Atchaneeyasakul, L M Linck, W E Connor, et al.Developmental Neuropsychology|January 6, 2001
Interhemispheric interaction during childhood: II. Children with early-treated phenylketonuriaM T Banich, A M Passarotti, D A White, et al.Biochemical and Biophysical Research Communications|May 25, 1995
Co-induction of arginase and nitric oxide synthase in murine macrophages activated by lipopolysaccharideW W Wang, C P Jenkinson, J M Griscavage, et al.Journal of Inherited Metabolic Disease|July 24, 2008
Correlates of language impairment in children with galactosaemiaN L Potter, J-A C Lazarus, J M Johnson, et al.Molecular Genetics and Metabolism|June 3, 1998
Cloning and characterization of the mouse and rat type II arginase genesR K Iyer, J M Bando, C P Jenkinson, et al.Pediatric Research|March 1, 1990
Guanidino compound analysis as a complementary diagnostic parameter for hyperargininemia: follow-up of guanidino compound levels during therapyB Marescau, P P De Deyn, A Lowenthal, et al.The Journal of Pediatrics|December 13, 2000
Risk factors for premature ovarian failure in females with galactosemiaN V Guerrero, R H Singh, A Manatunga, et al.Genetic Testing|January 11, 2000
A simple PCR-based assay allows detection of a common mutation, IVS8-1G-->C, in DHCR7 in Smith-Lemli-Opitz syndromeK P Battaile, C L Maslen, C A Wassif, et al.Pageof 10