User menu

The paradoxical association between inherited factor VII deficiency and venous thrombosis

Bibliographic reference Marty, S. ; Barro, C. ; Chatelain, Bernard ; Fimbel, B. ; Tribout, B. ; et. al. The paradoxical association between inherited factor VII deficiency and venous thrombosis. In: Haemophilia, Vol. 14, no. 3, p. 564-70 (2008)
Permanent URL
  1. Mariani G, Thromb Haemost, 93, 481 (2005)
  2. PEYVANDI F., MANNUCCI P. M., ASTI D., ABDOULLAHI M., DI ROCCO N., SHARIFIAN R., Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiency, 10.1046/j.1365-2516.1997.00137.x
  3. GOODNOUGH LAWRENCE T., SAITO HIDEHIKO, RATNOFF OSCAR D., Thrombosis or Myocardial Infarction in Congenital Clotting Factor Abnormalities and Chronic Thrombocytopenias : A Report of 21 Patients and a Review of 50 Previously Reported Cases, 10.1097/00005792-198307000-00004
  4. Escoffre M., Zini J. M., Schuamser L., Mazoyer E., Soria C., Tobelem G., Dupuy E., Severe arterial thrombosis in a congenitally factor VII deficient patient, 10.1111/j.1365-2141.1995.tb05378.x
  5. Gershwin M. Eric, Gude James K., Deep Vein Thrombosis and Pulmonary Embolism in Congenital Factor VII Deficiency, 10.1056/nejm197301182880309
  6. Sabharwal AK, Circulation, 88, 679 (1992)
  7. Giansily-Blaizot M, Haematologica, 89, 704 (2004)
  8. Giansily-Blaizot Muriel, , Aguilar-Martinez Patricia, Biron-Andreani Christine, Jeanjean Philippe, Igual Hélène, Schved Jean-François, Analysis of the genotypes and phenotypes of 37 unrelated patients with inherited factor VII deficiency, 10.1038/sj.ejhg.5200593
  9. Mariani G., Herrmann F. H., Schulman S., Batorova A., Wulff K., Etro D., Dolce A., Auerswald G., Astermark J., Schved J.-F., Ingerslev J., Bernardi F., , Thrombosis in inherited factor VII deficiency, 10.1046/j.1538-7836.2003.00395.x
  10. Lietz Katherine, Kuehling Stephanie E., Parkhurst Joan B., Hemorrhagic stroke in a child with protein S and factor VII deficiencies, 10.1016/j.pediatrneurol.2004.08.008
  11. Kang H.S., Kim D.G., Yoon B.-W., Superior Sagittal Sinus Thrombosis with Homocystinuria and Deficiency of Antithrombin III and Factor VII. Case Report, 10.1007/s007010050085
  12. Meissner Mark H., Chandler Wayne L., Elliott Jennifer S., Venous Thromboembolism in Trauma: A Local Manifestation of Systemic Hypercoagulability? : , 10.1097/01.ta.0000046253.33495.70
  13. Trojet S., Loukil I., El Afrit M.A., Mazlout H., Bousema F., Rokbani L., Kraiem A., Occlusion vasculaire rétinienne bilatérale au cours du syndrome des antiphospholipides, 10.1016/s0181-5512(05)81087-3
  14. Harmanci Ozgur, Ersoy Osman, Gurgey Aytemiz, Buyukasik Yahya, Gedikoglu Gokhan, Balkanci Ferhun, Sivri Bulent, Bayraktar Yusuf, The Etiologic Distribution of Thrombophilic Factors in Chronic Portal Vein Thrombosis : , 10.1097/01.mcg.0000225635.52780.47
  15. Wilde J.T., Evidence for the Use of Activated Prothrombin Complex Concentrates (aPCCs) in the Treatment of Patients with Haemophilia and Inhibitors, 10.1159/000057293
  16. Aledort L. M., Comparative thrombotic event incidence after infusion of recombinant factor VIIa versus factor VIII inhibitor bypass activity, 10.1111/j.1538-7836.2004.00944.x
  17. Ben Dridi MF, Arch Fr Pediatr, 43, 41 (1986)
  18. Kamphuisen P. W., Eikenboom J. C. J., Bertina R. M., Elevated Factor VIII Levels and the Risk of Thrombosis, 10.1161/01.atv.21.5.731
  19. Kyrle Paul A., Minar Erich, Hirschl Mirko, Bialonczyk Christine, Stain Milena, Schneider Barbara, Weltermann Ansgar, Speiser Wolfgang, Lechner Klaus, Eichinger Sabine, High Plasma Levels of Factor VIII and the Risk of Recurrent Venous Thromboembolism, 10.1056/nejm200008173430702
  20. Asherson R. A., Khanashta M. A., Hughes G. R. V., Antiphospholipid antibodies, lupus-like disease and the “primary” antiphospholipid syndrome, 10.1007/bf02031082
  21. Castoldi E., Coinheritance of Factor V (FV) Leiden enhances thrombin formation and is associated with a mild bleeding phenotype in patients homozygous for the FVII 9726+5G>A (FVII Lazio) mutation, 10.1182/blood-2003-04-1199
  22. Nichols WC, Blood, 88, 1183 (1996)
  23. Tizzano EF, Haematologica, 87, 279 (2002)
  24. Strey Rüdiger F., Siegemund Annelie, Siegemund Thomas, Schubert Christine, Schuster Gudrun, Wulff Karin, Herrmann Falko H., Influence of Factor V HR2 on Thrombin Generation and Clinical Manifestation in Rare Bleeding Disorders, 10.1159/000093108
  25. Giansily-Blaizot Muriel, Aguilar-Martinez Patricia, Briquel Marie-Elisabeth, d'Oiron Roseline, De Maistre Emmanuel, Epelbaum Serge, Schved Jean-François, Two novel cases of cerebral haemorrhages at the neonatal period associated with inherited factor VII deficiency, one of them revealing a new nonsense mutation (Ser52Stop) : , 10.1097/00001721-200302000-00016
  26. Hunault M, Blood, 93, 1237 (1999)
  27. Wulff Karin, Herrmann Falko H., Twenty two novel mutations of the factor VII gene in factor VII deficiency, 10.1002/1098-1004(200006)15:6<489::aid-humu1>;2-j
  28. Pinotti M, Blood, 92, 1646 (1998)
  29. Pinotti M, Blood, 95, 3423 (2000)
  30. Etro D, Haematologica, 88, 1434 (2003)
  31. O’Brien DP, Blood, 78, 132 (1991)
  32. TOSO Raffaella, PINOTTI Mirko, HIGH Katherine A., POLLAK Eleanor S., BERNARDI Francesco, A frequent human coagulation Factor VII mutation (A294V, c152) in loop 140s affects the interaction with activators, tissue factor and substrates, 10.1042/0264-6021:3630411
  33. Fromovich-Amit Y., Zivelin A., Rosenberg N., Tamary H., Landau M., Seligsohn U., Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patients, 10.1111/j.1538-7836.2004.00921.x
  34. MARIANI G., KONKLE B. A., INGERSLEV J., Congenital factor VII deficiency: therapy with recombinant activated factor VII - a critical appraisal, 10.1111/j.1365-2516.2006.01180.x
  35. GIROLAMI A., RUZZON E., TEZZA F., SCANDELLARI R., VETTORE S., GIROLAMI B., Arterial and venous thrombosis in rare congenital bleeding disorders: a critical review, 10.1111/j.1365-2516.2006.01299.x