Familial thrombophilia associated with fibrinogen Paris V: Dusart syndrome

Blood

Volumn 96, Issue 3, 2000, Pages 1191-1193

  Tarumi, Takashi ^a   Martincic, Danko ^a   Thomas, Anne ^a   Janco, Robert ^a   Hudson, Mary ^a   Baxter, Patricia ^a   Gailani, David ^a  

^a VANDERBILT UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 5 LEIDEN;

ARTICLE; CASE REPORT; CLINICAL FEATURE; DISEASE COURSE; DUSART SYNDROME; DYSFIBRINOGENEMIA; FAMILIAL DISEASE; FAMILY STUDY; GENETIC ANALYSIS; HUMAN; PEDIGREE; PRIORITY JOURNAL; THROMBOEMBOLISM;

EID: 0034254365     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v96.3.1191.015k47_1191_1193     Document Type: Article

References (17)

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5. Hereditary dysfibrinogenemia in a patient with thrombotic disease
6. A correlation between thrombotic disease and a specific fibrinogen abnormality (A-alpha 554 Arg to Cys) in two unrelated kindred, Dusart and Chapel Hill III
7. Dysfibrinogenemia (fibrinogen Dusard) associated with impaired fibrin- enhanced plasminogen activation
8. The relationship between the fibrinogen D domain self- association/cross-linking site (gamma-XL) and the fibrinogen Dusart abnormality (A-alpha R554C-albumin
9. Mutation in blood coagulation factor V associated with resistance to activated protein C
10. A common genetic variation in the 3-prime untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
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13. Post-operative deep vein thrombosis: Identifying high-risk patients
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15. Inherited thrombophilia, I
16. Molecular basis for fibrinogen Dusart (A- alpha 554 Arg to Cys) and its association with abnormal fibrin polymerization and thrombophilia
17. Mutation spectrum in fibrinogen genes: Molecular analysis in 11 German families with dysfibrinogenemia