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Journal of Inherited Metabolic Disease|January 1, 1992
3-Methylglutaconic aciduria: a marker for as yet unspecified disorders and the relevance of prenatal diagnosis in a 'new' type ('type 4')D Chitayat, J Chemke, K M Gibson, et al.The Journal of Pharmacology and Experimental Therapeutics|August 1, 1997
Endogenous natriuretic factors 7: biospecificity of a natriuretic gamma-tocopherol metabolite LLU-alphaE D Murray, W J Wechter, D Kantoci, et al.Molecular Genetics and Metabolism|March 2, 2010
Establishing a consortium for the study of rare diseases: The Urea Cycle Disorders ConsortiumJennifer Seminara, Mendel Tuchman, Lauren Krivitzky, et al.American Journal of Medical Genetics. Part A|February 19, 2016
Generating a taxonomy for genetic conditions relevant to reproductive planningDiane M Korngiebel, Carmit K McMullen, Laura M Amendola, et al.Enzyme|January 1, 1989
Mevalonate kinase in lysates of cultured human fibroblasts and lymphoblasts: kinetic properties, assay conditions, carrier detection and measurement of residual activity in a patient with mevalonic aciduriaK M Gibson, J L Lohr, R L Broock, et al.Journal of Lipid Research|March 1, 1990
3-Hydroxy-3-methylglutaryl coenzyme A reductase activity in cultured fibroblasts from patients with mevalonate kinase deficiency: differential response to lipid supplied by fetal bovine serum in tissue culture mediumK M Gibson, G Hoffmann, A Schwall, et al.Pharmacology Research & Perspectives|January 12, 2019
Preclinical tissue distribution and metabolic correlations of vigabatrin, an antiepileptic drug associated with potential use-limiting visual field defectsDana C Walters, Erwin E W Jansen, Garrett R Ainslie, et al.Journal of Inherited Metabolic Disease|January 1, 1988
3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: report of five new patientsK M Gibson, J Breuer, K Kaiser, et al.Molecular Genetics and Metabolism|March 13, 2001
Prenatal diagnosis of succinic semialdehyde dehydrogenase deficiency: increased accuracy employing DNA, enzyme, and metabolite analysesB M Hogema, S Akaboshi, M Taylor, et al.Clinical Chemistry|February 1, 1990
3-Hydroxy-3-methylglutaryl-CoA lyase deficiency as detected by radiochemical assay in cell extracts by thin-layer chromatography, and identification of three new casesK M Gibson, C F Lee, V Kamali, et al.Pageof 25