Disposition of homocysteine in subjects heterozygous for homocystinuria due to cystathionine ?-synthase deficiency: Relationship between genotype and phenotype

This publication has 36 references indexed in Scilit:

• Is the Oral Methionine Loading Test Insensitive to the Remethylation Pathway of Homocysteine?
  Blood, 1999
• Kinetic basis of hyperhomocysteinemia in patients with chronic renal failure
  Kidney International, 1997
• Plasma Homocysteine as a Risk Factor for Vascular Disease
  JAMA, 1997
• Variable hyperhomocysteinaemia phenotype in heterozygotes for the Gly307Ser mutation in cystathionine β‐synthase
  Australian and New Zealand Journal of Medicine, 1996
• Kinetics of total plasma homocysteine in subjects with hyperhomocysteinemia due to folate or cobalamin deficiency
  The American Journal of Clinical Nutrition, 1996
• Plasma homocysteine before and after methionine loading with regard to age, gender, and menopausal status
  European Journal of Clinical Investigation, 1992
• Persistent hypermethioninaemia with dominant inheritance
  Journal of Inherited Metabolic Disease, 1991
• The meaning and use of the area under a receiver operating characteristic (ROC) curve.
  Radiology, 1982
• The detection of heterozygotes for homocystinuria by oral loading with L-methionine
  Biochemical Journal, 1971
• Homocystinuria: Metabolic studies on 3 patients
  The Journal of Pediatrics, 1965