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S H Mudd

Showing results (61-70 of 93) with videos related to

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American 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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 6, 1975
Cystathioninuria and homocystinuriaH L Levy, S H Mudd, B W Uhlendorf, et al.
Plant Physiology|October 1, 1984
Threonine Synthase of Lemna paucicostata Hegelm. 6746J Giovanelli, K Veluthambi, G A Thompson, 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|November 1, 1982
Cardiovascular risk in heterozygotes for homocystinuriaS H Mudd, R Havlik, 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.
The Journal of Clinical Investigation|September 1, 1970
Homocystinuria due to cystathionine synthase deficiency: the effect of pyridoxineS H Mudd, W A Edwards, P M Loeb, et al.
Biochemical Medicine|December 1, 1970
Homocystinuria with methylmalonic aciduria: two cases in a sibshipS I Goodman, P G Moe, K B Hammond, 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.
Pageof 10

Showing results (61-70 of 93) with videos related to

Sort By:
Pageof 10
American 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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 6, 1975
Cystathioninuria and homocystinuriaH L Levy, S H Mudd, B W Uhlendorf, et al.
Plant Physiology|October 1, 1984
Threonine Synthase of Lemna paucicostata Hegelm. 6746J Giovanelli, K Veluthambi, G A Thompson, 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|November 1, 1982
Cardiovascular risk in heterozygotes for homocystinuriaS H Mudd, R Havlik, 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.
The Journal of Clinical Investigation|September 1, 1970
Homocystinuria due to cystathionine synthase deficiency: the effect of pyridoxineS H Mudd, W A Edwards, P M Loeb, et al.
Biochemical Medicine|December 1, 1970
Homocystinuria with methylmalonic aciduria: two cases in a sibshipS I Goodman, P G Moe, K B Hammond, 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.
Pageof 10