171 related articles for article (PubMed ID: 21453389)
1. Arg 304 Gln (FVII Padua) and Ala 294 Val mutations are equally present in patients with FVII deficiency and thrombosis.
Girolami A; Candeo N; Bonamigo E; Fabris F
Eur J Haematol; 2011 Jul; 87(1):92-4. PubMed ID: 21453389
[No 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. [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. PubMed ID: 22499055
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Pathogenetic role of Factor VII deficiency and thrombosis in cross-reactive material positive patients.
Girolami A; Sambado L; Bonamigo E; Ferrari S; Lombardi AM
Lab Hematol; 2013 Dec; 19(4):17-21. PubMed ID: 24370871
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [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]
8. [Analysis of an inherited FVII deficiency pedigree caused by homozygosity of Thr359Met].
Chu HY; Wang HL; Ding QL; Wang XF; Qu B; Wu F; Kang WY; Duan BH; Yin J; Fu QH; Wu WM; Wang ZY
Zhonghua Xue Ye Xue Za Zhi; 2003 Mar; 24(3):134-7. PubMed ID: 12697124
[TBL] [Abstract][Full Text] [Related]
9. Similarities and discrepancies in homozygous factor VII defects due to mutations in the region of residues Met298 to Cys310 (exon 8) in the catalytic domain of factor VII.
Girolami A; Berti de Marinis G; Bonamigo E; Vettore S
Lab Hematol; 2011 Jun; 17(2):17-21. PubMed ID: 21705315
[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. 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]
12. Twenty two novel mutations of the factor VII gene in factor VII deficiency.
Wulff K; Herrmann FH
Hum Mutat; 2000; 15(6):489-96. PubMed ID: 10862079
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. [An inherited coagulation factor VII deficiency pedigree caused by homozygous mutation of His348Gln].
Jin YH; Wang MS; Niu ZZ; Xie YS; Xie HX; Yang LH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Feb; 28(1):10-3. PubMed ID: 21287501
[TBL] [Abstract][Full Text] [Related]
15. Activated FVII levels in factor VII Padua (Arg304Gln) coagulation disorder and in true factor VII deficiency: a study in homozygotes and heterozygotes.
Girolami A; Bertozzi I; de Marinis GB; Bonamigo E; Fabris F
Hematology; 2011 Sep; 16(5):308-12. PubMed ID: 21902896
[TBL] [Abstract][Full Text] [Related]
16. Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain.
D'Andrea G; Bossone A; Lupone MR; Peyvandi F; Maisto G; Perricone F; Grandone E; Margaglione M
Haematologica; 2004 Aug; 89(8):979-84. PubMed ID: 15339682
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 22875495
[TBL] [Abstract][Full Text] [Related]
18. Characterization of a Cys329Gly mutation causing hereditary factor VII deficiency.
Wu Y; Tu X; Lian Y; Chen F; Lan F; Zhu Z
Acta Haematol; 2006; 116(2):96-100. PubMed ID: 16914903
[TBL] [Abstract][Full Text] [Related]
19. 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;
Haemophilia; 2009 Jan; 15(1):267-80. PubMed ID: 18976247
[TBL] [Abstract][Full Text] [Related]
20. [Two novel mutations in one pedigree with hereditary Factor VII deficiency].
Xing ZF; Wang XF; Dai J; Lu YL; Xu GQ; Xi XD; Wang HL
Zhonghua Xue Ye Xue Za Zhi; 2011 Mar; 32(3):158-62. PubMed ID: 21535952
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
