32 related articles for article (PubMed ID: 17938795)
1. Acute Thrombotic Events in Association With Coronavirus Disease of 2019 Immunization as Initial Presentation of Congenital Factor VII Deficiency.
Trillo A; Davis JA; Sargenton K; Corrales-Medina FF
J Pediatr Hematol Oncol; 2023 Aug; 45(6):e781-e783. PubMed ID: 37494615
[TBL] [Abstract][Full Text] [Related]
2. The paradoxical association between inherited factor VII deficiency and venous thrombosis.
Marty S; Barro C; Chatelain B; Fimbel B; Tribout B; Reynaud J; Schved JF; Giansily-Blaizot M
Haemophilia; 2008 May; 14(3):564-70. PubMed ID: 18282149
[TBL] [Abstract][Full Text] [Related]
3. Complexity of the genetic contribution to factor VII deficiency in two Spanish families: clinical and biological implications.
Sabater-Lleal M; Martínez-Marchán E; Martínez-Sánchez E; Coll M; Vallvé C; Mateo J; Souto JC; Fontcuberta J; Soria JM
Haematologica; 2003 Aug; 88(8):906-13. PubMed ID: 12935978
[TBL] [Abstract][Full Text] [Related]
4. Factor VII and fibrinogen levels as risk factors for venous thrombosis. A case-control study of plasma levels and DNA polymorphisms--the Leiden Thrombophilia Study (LETS).
Koster T; Rosendaal FR; Reitsma PH; van der Velden PA; Briët E; Vandenbroucke JP
Thromb Haemost; 1994 Jun; 71(6):719-22. PubMed ID: 7974338
[TBL] [Abstract][Full Text] [Related]
5. Fibrinogen, factor VII and PAI-1 genotypes and the risk of coronary and peripheral atherosclerosis: Edinburgh Artery Study.
Lee AJ; Fowkes FG; Lowe GD; Connor JM; Rumley A
Thromb Haemost; 1999 Apr; 81(4):553-60. PubMed ID: 10235438
[TBL] [Abstract][Full Text] [Related]
6. Coagulation factor VII R353Q polymorphism and the risk of puerperal cerebral venous thrombosis.
Kruthika-Vinod TP; Nagaraja D; Christopher R
J Clin Neurosci; 2012 Jan; 19(1):190-1. PubMed ID: 22136731
[TBL] [Abstract][Full Text] [Related]
7. A two adenine insertion polymorphism in the 3' untranslated region of factor VII gene is associated with peripheral arterial disease but not with venous thrombosis. Results of case-control studies.
Serve E; Reny JL; Akhavan S; Emmerich J; Fischer AM; Tapon-Bretaudière J
Thromb Haemost; 2007 Oct; 98(4):733-7. PubMed ID: 17938795
[TBL] [Abstract][Full Text] [Related]
8. [Type I antithrombin deficiency as a cause of arterial and venous thrombosis in a family with severe thrombophilia].
Tóth O; Dávid M; Habon T; Nagy A; Keszthelyi Z; Kovács N; Losonczy H
Orv Hetil; 2005 Oct; 146(41):2121-5. PubMed ID: 16304806
[TBL] [Abstract][Full Text] [Related]
9. Potential predictors of bleeding risk in inherited factorVII deficiency. Clinical, biological and molecular criteria.
Giansily-Blaizot M; Schved JF
Thromb Haemost; 2005 Nov; 94(5):901-6. PubMed ID: 16363229
[TBL] [Abstract][Full Text] [Related]
10. How to evaluate phenotype-genotype relationship in rare coagulation haemorrhagic disorders: examples from FVII deficiency.
Bernardi F; Marchetti G; Dolce A; Mariani G
Haemophilia; 2004 Oct; 10 Suppl 4():177-9. PubMed ID: 15479394
[TBL] [Abstract][Full Text] [Related]
11. Congenital FVII deficiency and pulmonary embolism: a critical appraisal of all reported cases.
Girolami A; Berti de Marinis G; Vettore S; Girolami B
Clin Appl Thromb Hemost; 2013; 19(1):55-9. PubMed ID: 22327818
[TBL] [Abstract][Full Text] [Related]
12. Links between arterial and venous disease.
Prandoni P
J Intern Med; 2007 Sep; 262(3):341-50. PubMed ID: 17697155
[TBL] [Abstract][Full Text] [Related]
13.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
