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Items: 1 to 20 of 114

1.

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
2.

Factor VII Deficiency.

Mariani G, Bernardi F.

Semin Thromb Hemost. 2009 Jun;35(4):400-6. doi: 10.1055/s-0029-1225762. Epub 2009 Jul 13. Review.

PMID:
19598068
3.

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. Epub 2013 Mar 21.

PMID:
23571462
4.

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
5.

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. Epub 2013 Jun 4.

PMID:
23731332
6.

Genotype associations of factor VII gene with plasma factor VII coagulant activity and antigen levels in healthy Chinese.

Liu Y, Heng CK, Saha N, Hong S, Low PS.

Blood Coagul Fibrinolysis. 2002 Apr;13(3):217-24.

PMID:
11943935
7.

Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene.

Herrmann FH, Wulff K, Auerswald G, Schulman S, Astermark J, Batorova A, Kreuz W, Pollmann H, Ruiz-Saez A, De Bosch N, Salazar-Sanchez L; Greifswald Factor FVII Deficiency Study Group..

Haemophilia. 2009 Jan;15(1):267-80. doi: 10.1111/j.1365-2516.2008.01910.x. Epub 2008 Oct 30.

PMID:
18976247
8.

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
9.

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.

10.

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. Epub 2013 Aug 28.

PMID:
23992369
11.

Congenital Factor VII Deficiency in Children at Tertiary Health Care Facility in Pakistan.

Alam MM, Moiz B, Rehman KA, Jethwani P, Fadoo Z.

Clin Appl Thromb Hemost. 2015 Oct;21(7):639-44. doi: 10.1177/1076029613515070. Epub 2013 Dec 9.

PMID:
24322277
12.

Molecular and clinical aspects of factor VII deficiency.

Mariani G, Lo Coco L, Bernardi F, Pinotti M.

Blood Coagul Fibrinolysis. 1998 Mar;9 Suppl 1:S83-8.

PMID:
9819034
13.

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
14.

[Genotype and phenotype analysis of congenital coagulator factor VII deficiency in four Chinese pedigrees].

Jiang MH, Wang ZY, Yu ZQ, Bai X, Cao LJ, Su J, Sun XH, Zhang W, Ruan CG.

Zhonghua Xue Ye Xue Za Zhi. 2011 Mar;32(3):147-52. Chinese.

PMID:
21535950
15.

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.

Castoldi E, Govers-Riemslag JW, Pinotti M, Bindini D, Tans G, Berrettini M, Mazzucconi MG, Bernardi F, Rosing J.

Blood. 2003 Dec 1;102(12):4014-20. Epub 2003 Jul 24.

16.

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].

17.

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].

18.

Recurrent mutations and genotype-phenotype correlations in hereditary factor VII deficiency in Korea.

Kwon MJ, Yoo KY, Lee KO, Kim SH, Kim HJ.

Blood Coagul Fibrinolysis. 2011 Mar;22(2):102-5. doi: 10.1097/MBC.0b013e328343641a.

PMID:
21206266
19.

Factor VII Arg/Gln353 polymorphism determines factor VII coagulant activity in patients with myocardial infarction (MI) and control subjects in Belfast and in France but is not a strong indicator of MI risk in the ECTIM study.

Lane A, Green F, Scarabin PY, Nicaud V, Bara L, Humphries S, Evans A, Luc G, Cambou JP, Arveiler D, Cambien F.

Atherosclerosis. 1996 Jan 5;119(1):119-27.

PMID:
8929253
20.

Long-term prophylaxis in severe factor VII deficiency.

Siboni SM, Biguzzi E, Mistretta C, Garagiola I, Peyvandi F.

Haemophilia. 2015 Nov;21(6):812-9. doi: 10.1111/hae.12702. Epub 2015 May 8.

PMID:
25952977

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