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Analytical Biochemistry|August 15, 1988
Interference of 3-hydroxyisobutyrate with measurements of ketone body concentration and isotopic enrichment by gas chromatography-mass spectrometryC Des Rosiers, J A Montgomery, S Desrochers, et al.The Journal of Pediatrics|July 1, 1992
Brain dysgenesis and congenital intracerebral calcification associated with 3-hydroxyisobutyric aciduriaD Chitayat, K Meagher-Villemure, O A Mamer, et al.Molecular Genetics and Metabolism|July 20, 2001
In vivo variability of TMA oxidation is partially mediated by polymorphisms of the FMO3 geneD M Lambert, O A Mamer, B R Akerman, et al.Neurology|January 1, 1975
The syndrome of systemic carnitine deficiency. Clinical, morphologic, biochemical, and pathophysiologic featuresG Karpati, S Carpenter, A G Engel, et al.Molecular Genetics and Metabolism|September 10, 1999
Trimethylaminuria is caused by mutations of the FMO3 gene in a North American cohortB R Akerman, H Lemass, L M Chow, et al.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 American Journal of Physiology|March 1, 1990
Pseudoketogenesis in hepatectomized dogsC Des Rosiers, J A Montgomery, M Garneau, et al.Pageof 6