Higher total plasma homocysteine in vitamin B12 deficiency than in heterozygosity for homocystinuria due to cystathionine β-synthase deficiency

Metabolism

Volumn 37, Issue 2, 1988, Pages 175-178

  Brattström, Lars ^a,b   Israelsson, Bo ^a,b   Lindgärde, Folke ^a,b   Hultberg, Björn ^a,b  

^a LUND UNIVERSITY   (Sweden)

^b LUND UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

HOMOCYSTEINE;

CYANOCOBALAMIN DEFICIENCY; FEMALE; HOMOCYSTINURIA; HUMAN; HUMAN EXPERIMENT; MALE; NORMAL HUMAN; THROMBOEMBOLISM;

CYSTATHIONINE BETA-SYNTHASE; HETEROZYGOTE; HOMOCYSTEINE; HOMOCYSTINURIA; HUMAN; HYDRO-LYASES; SUPPORT, NON-U.S. GOV'T; VASCULAR DISEASES; VITAMIN B 12; VITAMIN B 12 DEFICIENCY;

EID: 0023832738     PISSN: 00260495     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0026-0495(98)90014-2     Document Type: Article

References (27)

1. Disorders of transsulfuration
2. Homocysteine theory of arteriosclerosis
3. Heterozygosity for homocystinuria in premature peripheral and cerebral occlusive arterial disease
4. The pathogenesis of coronary artery disease: A possible role for methionine metabolism
5. Moderate homocysteinemia—a possible risk factor for arteriosclerotic cerebrovascular disease
6. Methionine intolerance: A possible risk factor for coronary artery disease
7. Protein-bound homocyst(e)ine—a possible risk factor for coronary artery disease
8. Plasma homocysteine and coronary artery disease
9. Homocysteinemia, ischemic heart disease, and the carrier state for homocystinuria
10. Homocystinuria, Addisonian pernicious anaemia, and partial deletion of a G chromosome (Letter)
11. Homocystinuria and organic aciduria in a patient with vitamin-B12 deficiency (Letter)
12. A syndrome of methylmalonic aciduria homocysteinuria megaloblastic anemia and neurological abnormalities in a vitamin B12-deficient breast-fed infant of a strict vegetarian
13. Homocysteinemia due to folate deficiency
14. Cytochemical detection of homocysteine in pernicious anemia and in chronic erythremic myelosis
15. Quantitation of total homocysteine, total cysteine, and methionine in normal serum and urine using capillary gas chromatography-mass spectrometry
16. Vascular pathology of homocysteinemia: Implications for the pathogenesis of arteriosclerosis
17. Congenital defect in intracellular cobalamin metabolism resulting in homocystinuria and methylmalonic aciduria
18. Inborn errors of folate metabolism
19. An inborn error of vitamin B12 metabolism associated with cellular deficiency of coenzyme forms of the vitamin
20. Abnormal deoxyuridine suppression test in congenital metylmalonic aciduria-homocystinuria without megaloblastic anemia: Divergent biochemical and morphological bone marrow manifestations of disordered cobalamin metabolism in man
21. The protective effect of pernicious anemia on the development of atherosclerosis: a comparative study
22. Association between anaemia and hypolipidaemia (Letter)
23. Studies on plasma lipid and phospholipid composition in pernicious anemia before and after specific treatment
24. Acquired thrombocytopathy in patients with pernicious anaemia
25. A qualitative platelet defect in severe vitamin B12 deficiency
26. Platelet dysfunction in patients with vitamin B12 deficiency
27. Homocystine-induced arteriosclerosis, the role of endothelial cell injury and platelet response in its genesis