These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. Inherited factor VII deficiency: genetics and molecular pathology. Tuddenham EG; Pemberton S; Cooper DN Thromb Haemost; 1995 Jul; 74(1):313-21. PubMed ID: 8578478 [No Abstract] [Full Text] [Related]
3. [Molecular abnormality and deficiency of coagulation factor VII]. Ichinose A Ryoikibetsu Shokogun Shirizu; 1998; (21 Pt 2):460-3. PubMed ID: 9833542 [No Abstract] [Full Text] [Related]
4. 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. PubMed ID: 10959697 [TBL] [Abstract][Full Text] [Related]
5. Asymptomatic factor VII deficiency: gene analysis and structure-function relationships. Kirkel D; Lin TW; Fu SW; Dlott JS; Sahud MA; McCaffrey T; Rickles FR Blood Coagul Fibrinolysis; 2010 Jan; 21(1):91-4. PubMed ID: 20040857 [TBL] [Abstract][Full Text] [Related]
6. Severe factor VII deficiency caused by a novel point mutation (Arg353Pro) combined with a rare Cys22Arg mutation. Zhidong W; Xiaojun H Thromb Haemost; 2007 Sep; 98(3):687-8. PubMed ID: 17849063 [No Abstract] [Full Text] [Related]
7. Characterization of a factor VII molecule carrying a mutation in the second epidermal growth factor-like domain. Kavlie A; Orning L; Grindflek A; Stormorken H; Prydz H Thromb Haemost; 1998 Jun; 79(6):1136-43. PubMed ID: 9657438 [TBL] [Abstract][Full Text] [Related]
8. Genotypic heterogeneity may explain phenotypic variations in inherited factor VII deficiency. Giansily-Blaizot M; Aguilar-Martinez P; Schved JF Haematologica; 2002 Mar; 87(3):328-9. PubMed ID: 11869950 [TBL] [Abstract][Full Text] [Related]
9. Severe factor VII deficiency caused by a novel mutation His348 to Gln in the catalytic domain. Katsumi A; Matsushita T; Yamazaki T; Sugiura I; Kojima T; Saito H Thromb Haemost; 2000 Feb; 83(2):239-43. PubMed ID: 10739380 [TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 15907525 [TBL] [Abstract][Full Text] [Related]
11. Molecular analysis in a patient with severe factor VII deficiency and an inhibitor: report of a novel mutation (S103G). Pruthi RK; Rodriguez V; Allen C; Slaby JA; Schmidt KA; Plumhoff EA Eur J Haematol; 2007 Oct; 79(4):354-9. PubMed ID: 17692102 [TBL] [Abstract][Full Text] [Related]
12. [Novel double heterozygous mutations on Met306Val and Thr181Asn related to a hereditary coagulation factor VII deficiency]. Tu CQ; Deng CY; Wu JZ; Pan CY; Xie CY Zhonghua Yi Xue Za Zhi; 2006 Jan; 86(2):124-7. PubMed ID: 16620721 [TBL] [Abstract][Full Text] [Related]
13. Characterization of mild coagulation factor VII deficiency: activity and clearance of the Arg315Trp and Arg315Lys variants in the Cys310-Cys329 loop (c170s). Furlan Freguia C; Toso R; Pollak ES; Arruda VR; Pinotti M; Bernardi F Haematologica; 2004 Dec; 89(12):1504-9. PubMed ID: 15590402 [TBL] [Abstract][Full Text] [Related]
14. The extrinsic pathway inhibitor: a regulator of tissue factor-dependent blood coagulation. Rapaport SI Thromb Haemost; 1991 Jul; 66(1):6-15. PubMed ID: 1926052 [No Abstract] [Full Text] [Related]
15. Variability of clinical manifestation of factor VII-deficiency in homozygous and heterozygous subjects of the European F7 gene mutation A294V. Herrmann FH; Wulff K; Strey R; Siegemund A; Astermark J; Schulman S; Haematologica; 2008 Aug; 93(8):1273-5. PubMed ID: 18556408 [No Abstract] [Full Text] [Related]
17. Factor VII and haemostasis: interaction between abnormal factors VII and tissue thromboplastins. Girolami A; Simioni P; Steffan A Blood Coagul Fibrinolysis; 1990 Dec; 1(6):749-50. PubMed ID: 2133255 [No Abstract] [Full Text] [Related]
18. 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]
19. [Studies on inherited coagulation factor VII deficiency and tissue factor abnormality in a pedigree]. Ding QL; Wang XF; Xu GQ; Huang XP; Hu YQ; Wu WM; Fu QH; Wang HL; Wang ZY Zhonghua Xue Ye Xue Za Zhi; 2006 Mar; 27(3):150-3. PubMed ID: 16792912 [TBL] [Abstract][Full Text] [Related]
20. [Inherited coagulation factor VII deficiency caused by double heterozygotic mutations Arg304Gln and Arg304Trp]. Ding QL; Wang HL; Wang XF; Wang MS; Fu QH; Wu WM; Hu YQ; Wang ZY Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):279-83. PubMed ID: 12903033 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]