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Clinica Chimica Acta; International Journal of Clinical Chemistry|January 6, 1975
Cystathioninuria and homocystinuriaH L Levy, S H Mudd, B W Uhlendorf, et al.Pediatric Research|March 1, 1976
Cobalamins in fibroblasts cultured from normal control subjects and patients with methylmalonic aciduriaJ C Linnell, D M Matthews, S H Mudd, et al.Research Communications in Chemical Pathology and Pharmacology|February 1, 1989
Homocysteine thiolactone: failure to detect in human serum or plasmaS H Mudd, A I Matorin, H L LevyAmerican Journal of Obstetrics and Gynecology|September 16, 1999
Maternal gamma-cystathionase deficiency: absence of both teratogenic effects and pregnancy complicationsJ E Vargas, S H Mudd, S E Waisbren, et al.American Journal of Human Genetics|November 1, 1981
A study of cardiovascular risk in heterozygotes for homocystinuriaS H Mudd, R Havlik, H L Levy, 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.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.Metabolism: Clinical and Experimental|January 6, 2001
Isolated hypermethioninemia: measurements of S-adenosylmethionine and cholineS H Mudd, D J Jenden, A Capdevila, et al.The Journal of Clinical Investigation|October 1, 1995
Molecular mechanisms of an inborn error of methionine pathway. Methionine adenosyltransferase deficiencyT Ubagai, K J Lei, S Huang, et al.Cell Differentiation|August 1, 1985
The differentiation of L5/A10 myoblast cell line (a subclone of L5 line) is controlled by changes of culture conditionsS Scarpa, B W Uhlendorf, G L CantoniPageof 19