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Items: 1 to 20 of 95

1.

Bleeding symptoms at disease presentation and prediction of ensuing bleeding in inherited FVII deficiency.

Di Minno MN, Dolce A, Mariani G; STER Study Group..

Thromb Haemost. 2013 Jun;109(6):1051-9. doi: 10.1160/TH12-10-0740.

PMID:
23571462
2.

Replacement therapy for bleeding episodes in factor VII deficiency. A prospective evaluation.

Mariani G, Napolitano M, Dolce A, Pérez Garrido R, Batorova A, Karimi M, Platokouki H, Auerswald G, Bertrand AM, Di Minno G, Schved JF, Bjerre J, Ingerslev J, Sørensen B, Ruiz-Saez A; Seven Treatment Evaluation Registry.; International Factor VII Deficiency Study Group..

Thromb Haemost. 2013 Feb;109(2):238-47. doi: 10.1160/TH12-07-0476.

PMID:
23238632
3.

Analysis of biological phenotypes from 42 patients with inherited factor VII deficiency: can biological tests predict the bleeding risk?

Giansily-Blaizot M, Verdier R, Biron-Adréani C, Schved JF, Bertrand MA, Borg JY, Le Cam-Duchez V, Briquel ME, Chambost H, Pouymayou K, Dutrillaux F, Favier R, Martin-Toutain I, Verdy E, Gay V, Goudemand J, Navarro R, Durin A, d'Oiron R, Lambert T, Pernod G, Barrot C, Peynet J, Bastenaire B, Sie P, Stieltjes N, Torchet MF, de Moerloose P; Study group of FVII deficiency..

Haematologica. 2004 Jun;89(6):704-9. Erratum in: Haematologica. 2007 Nov;92(11):1584. LeCam-Duchez, V [corrected to Le Cam-Duchez, V].

4.

Women with congenital factor VII deficiency: clinical phenotype and treatment options from two international studies.

Napolitano M, Di Minno MN, Batorova A, Dolce A, Giansily-Blaizot M, Ingerslev J, Schved JF, Auerswald G, Kenet G, Karimi M, Shamsi T, Ruiz de Sáez A, Dolatkhah R, Chuansumrit A, Bertrand MA, Mariani G.

Haemophilia. 2016 Sep;22(5):752-9. doi: 10.1111/hae.12978.

PMID:
27338009
5.

Use of thromboelastography and thrombin generation assay to predict clinical phenotype in patients with severe FVII deficiency.

Tran HT, Tjønnfjord GE, Holme PA.

Haemophilia. 2014 Jan;20(1):141-6. doi: 10.1111/hae.12256.

PMID:
23992369
6.

Clinical phenotypes and factor VII genotype in congenital factor VII deficiency.

Mariani G, Herrmann FH, Dolce A, Batorova A, Etro D, Peyvandi F, Wulff K, Schved JF, Auerswald G, Ingerslev J, Bernardi F; International Factor VII Deficiency Study Group..

Thromb Haemost. 2005 Mar;93(3):481-7.

PMID:
15735798
7.

Factor VII deficiency: defining the clinical picture and optimizing therapeutic options.

Lapecorella M, Mariani G; International Registry on Congenital Factor VII Deficiency..

Haemophilia. 2008 Nov;14(6):1170-5. doi: 10.1111/j.1365-2516.2008.01844.x. Review.

PMID:
19141157
8.

Use of global assays to understand clinical phenotype in congenital factor VII deficiency.

Greene LA, Goldenberg NA, Simpson ML, Villalobos-Menuey E, Bombardier C, Acharya SS, Santiago-Borrero PJ, Cambara A, DiMichele DM.

Haemophilia. 2013 Sep;19(5):765-72. doi: 10.1111/hae.12160.

PMID:
23682803
9.

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. doi: 10.1111/j.1365-2516.2007.01647.x.

PMID:
18282149
10.

Genotype and phenotype relationships in 10 Pakistani unrelated patients with inherited factor VII deficiency.

Borhany M, Boijout H, Pellequer JL, Shamsi T, Moulis G, Aguilar-Martinez P, Schved JF, Giansily-Blaizot M.

Haemophilia. 2013 Nov;19(6):893-7. doi: 10.1111/hae.12186.

PMID:
23731332
11.

Prevalence of factor VII deficiency and molecular characterization of the F7 gene in Brazilian patients.

Rodrigues DN, Siqueira LH, Galizoni AM, Arruda VR, Annichino-Bizzacchi JM.

Blood Coagul Fibrinolysis. 2003 Apr;14(3):289-92.

PMID:
12695753
12.

The significance of published polymorphisms in 14 cases of mild factor VII deficiency.

Cutler JA, Patel R, Mitchell MJ, Savidge GF.

Blood Coagul Fibrinolysis. 2005 Mar;16(2):91-5.

PMID:
15741795
13.

Inherited factor VII deficiency and surgery: clinical data are the best criteria to predict the risk of bleeding.

Giansily-Blaizot M, Biron-Andreani C, Aguilar-Martinez P, de Moeloose P, Briquel ME, Goudemand J, Stieltjes N, Barrot C, Chambost H, Durin A, Gay V, Peynet J, Pouymayou K, Schved JF.

Br J Haematol. 2002 Apr;117(1):172-5.

PMID:
11918551
14.

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. Review.

PMID:
16363229
15.

Inherited factor VII deficiency: identification of two novel mutations (A191V and T239P) in the catalytic domain.

Borensztajn K, Chafa O, Le Bonniec B, Wajcman H, Reghis A, Fischer AM, Tapon-Bretaudière J.

Thromb Res. 2005;116(2):115-20.

PMID:
15907525
16.

Residual factor VII activity and different hemorrhagic phenotypes in CRM(+) factor VII deficiencies (Gly331Ser and Gly283Ser).

Pinotti M, Etro D, Bindini D, Papa ML, Rodorigo G, Rocino A, Mariani G, Ciavarella N, Bernardi F.

Blood. 2002 Feb 15;99(4):1495-7. Erratum in: Blood 2001 Apr 1;99(7):2290. Pinotti, Marko [corrected to Pinotti, Mirko]; Etro, Dániela [corrected to Etro, Daniela]; Mariani, Guglieuto [corrected to Mariani, Guglielmo].

17.

[Molecular genetics and clinical features of nine patients with inherited coagulation factor VII deficiency].

Jin YH, Wang MS, Zheng FX, Xie YS, Xie HX, Xu PF.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):404-7. doi: 10.3760/cma.j.issn.1003-9406.2012.04.006. Chinese.

PMID:
22875495
18.

[Significant decrease in factor VII activity by tissue thromboplastin derived from rabbit brain in a patient with congenital factor VII deficiency (FVII Padua)].

Sekiya A, Morishita E, Maruyama K, Asakura H, Nakao S, Ohtake S.

Rinsho Ketsueki. 2012 Mar;53(3):357-60. Japanese.

PMID:
22499055
19.

Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias.

Acharya SS, Coughlin A, Dimichele DM; North American Rare Bleeding Disorder Study Group..

J Thromb Haemost. 2004 Feb;2(2):248-56.

20.

Molecular characterisation and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiency.

Peyvandi F, Jenkins PV, Mannucci PM, Billio A, Zeinali S, Perkins SJ, Perry DJ.

Thromb Haemost. 2000 Aug;84(2):250-7.

PMID:
10959697

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