Homocysteinemia and recurrent fetal losses: Description of three cases;Homocystéine et fausses couches: À propos de trois cas cliniques

Annales de Biologie Clinique

Volumn 60, Issue 3, 2002, Pages 325-326

  Barro, C ^a   Ducros, V ^a   Bonaz, B ^a   Muet, F ^a   Quenard, N ^a   Fontaine, M ^a   Polack, B ^a   Pernod, G ^a  

^a GRENOBLE UNIVERSITY HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL MARKER; HOMOCYSTEINE; VITAMIN;

ADULT; BLOOD; CASE REPORT; CONFERENCE PAPER; FEMALE; FETUS; FETUS WASTAGE; GENOTYPE; HOMOCYSTINURIA; HOMOZYGOTE; HUMAN; PREGNANCY; PROPHYLAXIS; RECURRENT ABORTION; RECURRENT DISEASE; RISK FACTOR; VITAMIN SUPPLEMENTATION; ARTICLE;

ABORTION, HABITUAL; ADULT; BIOLOGICAL MARKERS; FEMALE; HOMOCYSTEINE; HUMANS; PREGNANCY;

EID: 2242435235     PISSN: 00033898     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (6)

1. A candidate genetic risk factor for vascular disease: A common mutation in methylene tetrahydrofolate reductase
2. The factor V Leiden mutation may predispose women to severe preeclampsia
3. Increased fetal loss in women with heritable thrombophilia
4. Factor V Leiden, C > T MTHFR polymorphism and genetic susceptibility to preeclampsia
5. Genetic susceptibility to pregnancy-related venous thromboembolism: Roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations
6. Facteur V Leiden, hyperhomocystéinémie, mutation C677T de la MTHFR, mutation G20210A de la prothrombine et complications obstétricales