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American Journal of Ophthalmology|August 1, 1980
Epileptiform ocular movements with methylmalonic aciduria and homocystinuriaD G Cogan, J Schulman, R J Porter, et al.
The Journal of Clinical Investigation|May 1, 1975
Homocystinuria due to cystathionine synthase deficiency. Studies of nitrogen balance and sulfur excretionJ R Poole, S H Mudd, E B Conerly, et al.
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.
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.
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.
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.
Metabolism: Clinical and Experimental|January 6, 2001
Isolated hypermethioninemia: measurements of S-adenosylmethionine and cholineS H Mudd, D J Jenden, A Capdevila, et al.
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