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Journal of Inherited Metabolic Disease|December 31, 1998
One-methyl group metabolism in non-ketotic hyperglycinaemia: mildly elevated cerebrospinal fluid homocysteine levelsJ L Van Hove, F Lazeyras, S H Zeisel, et al.The Journal of Nutrition|April 4, 2001
Nutrition: a reservoir for integrative scienceS H Zeisel, L H Allen, S P Coburn, et al.Journal of Inherited Metabolic Disease|June 1, 2006
S-adenosylhomocysteine hydrolase deficiency in a 26-year-old manN R M Buist, B Glenn, O Vugrek, et al.Journal of Chromatography. B, Biomedical Sciences and Applications|September 4, 2001
Quantitative analysis of the principle soy isoflavones genistein, daidzein and glycitein, and their primary conjugated metabolites in human plasma and urine using reversed-phase high-performance liquid chromatography with ultraviolet detectionB F Thomas, S H Zeisel, M G Busby, et al.The Journal of Nutrition|July 1, 2005
The nutritional phenotype in the age of metabolomicsS H Zeisel, H C Freake, D E Bauman, et al.The Journal of Nutrition|October 7, 2004
Metabolomics in the opening decade of the 21st century: building the roads to individualized healthJ B German, D E Bauman, D G Burrin, et al.Journal of Inherited Metabolic Disease|January 26, 2006
S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapyI Barić, M Cuk, K Fumić, et al.Pageof 11