Cerebral venous thrombosis and familiar prothrombin gene G20210A mutation;Trombosis venosa cerebral y mutación G20210A del gen de la protrombina familiar

Revista de Neurologia

Volumn 33, Issue 4, 2001, Pages 335-338

  Verdelho, A ^a   Ferro, J M ^a   Palmeiro, A ^a   Antunes, C ^a  

^a HOSPITAL DE SANTA MARIA   (Portugal)

Author keywords

Cerebral venous thrombosis; Familiar; Prothrombin gene mutation

Indexed keywords

ANTICOAGULANT AGENT; ANTITHROMBOCYTIC AGENT; CARDIOLIPIN ANTIBODY; PROTHROMBIN;

ADULT; ANTIBODY TITER; ANTICOAGULANT THERAPY; ARTICLE; CASE REPORT; CEREBROVASCULAR DISEASE; DEEP VEIN THROMBOSIS; FAMILY HISTORY; FEMALE; GENE MUTATION; HUMAN; OCCLUSIVE CEREBROVASCULAR DISEASE; PEDIGREE ANALYSIS;

EID: 0035899156     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: 10.33588/rn.3304.2001150     Document Type: Article

References (14)

1. Venous thrombosis: A multicausal disease
2. A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
3. The 20210A allele of the prothrombin gene is a common risk factor among Swedish outpatient with verified deep venous thrombosis
4. Risk of venous thromboembolism associated with a G to A transition at position 20210 in the 3 '-untranslated region of the prothrombin gene
5. Increased risk for venous thrombosis in the carriers of the prothrombin G-A 20210 gene variant
6. Deep-vein thrombosis
7. Coincidence of factor V Leiden mutation and a mutation in the prothrombin gene at position 20210 in a patient with puerperal cerebral venous thrombosis
8. High risk of cerebral-vein thrombosis in carriers of a prothrombin-gene mutation and in users of oral contraceptives
9. Frequency of the 20210 G→A mutation in the 3'-untranslated region of the prothrombin gene in 35 cases of cerebral venous thrombosis
10. Prothrombin gene G20210→A transition is a risk factor for cerebral venous thrombosis
11. Superior sagittal sinus thrombosis in a patient heterozygotous for the novel 20210→A allele of the prothrombin gene
12. Inherited prothrombotic risk factors and cerebral venous thrombosis
13. G20210→A Prothrombin gene mutation in two siblings with cerebral venous thrombosis
14. Prevalence of the prothrombin gene variant in the venous thrombosis and arterial disease