274 related articles for article (PubMed ID: 17614823)
1. Characterisation of a large complex intragenic re-arrangement in the FVII gene (F7) avoiding misdiagnosis in inherited factor VII deficiency.
Giansily-Blaizot M; Thorel D; Khau Van Kien P; Behar C; Romey MC; Mugneret F; Schved JF; Claustres M
Br J Haematol; 2007 Aug; 138(3):359-65. PubMed ID: 17614823
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Severe FVII deficiency caused by a new point mutation combined with a previously undetected gene deletion.
Hewitt J; Ballard JN; Nelson TN; Smith VC; Griffiths TA; Pritchard S; Wu JK; Wadsworth LD; Casey B; MacGillivray RT
Br J Haematol; 2005 Feb; 128(3):380-5. PubMed ID: 15667541
[TBL] [Abstract][Full Text] [Related]
4. 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. PubMed ID: 12935978
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [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]
7. [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]
8. Analysis of the genotypes and phenotypes of 37 unrelated patients with inherited factor VII deficiency.
Giansily-Blaizot M; Aguilar-Martinez P; Biron-Andreani C; Jeanjean P; Igual H; Schved JF;
Eur J Hum Genet; 2001 Feb; 9(2):105-12. PubMed ID: 11313743
[TBL] [Abstract][Full Text] [Related]
9. 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. PubMed ID: 12695753
[TBL] [Abstract][Full Text] [Related]
10. [Genetic analysis of hereditary factor VII deficiency from a Chinese pedigree].
Wu Y; Yang W; Fang G
Zhonghua Yi Xue Za Zhi; 2000 Dec; 80(12):904-6. PubMed ID: 11236630
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. 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]
13. Factor VII Mie: homozygous asymptomatic type I deficiency caused by an amino acid substitution of His (CAC) for Arg(247) (CGC) in the catalytic domain.
Ohiwa M; Hayashi T; Wada H; Minamikawa K; Shirakawa S; Suzuki K
Thromb Haemost; 1994 Jun; 71(6):773-7. PubMed ID: 7974346
[TBL] [Abstract][Full Text] [Related]
14. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
15. F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency. Results from a genotype-phenotype study.
Quintavalle G; Riccardi F; Rivolta GF; Martorana D; Di Perna C; Percesepe A; Tagliaferri A;
Thromb Haemost; 2017 Aug; 117(8):1455-1464. PubMed ID: 28447100
[TBL] [Abstract][Full Text] [Related]
16. Familial factor VII deficiency with foetal and neonatal fatal cerebral haemorrhage associated with homozygosis to Gly180Arg mutation.
Landau D; Rosenberg N; Zivelin A; Staretz-Chacham O; Kapelushnik J
Haemophilia; 2009 May; 15(3):774-8. PubMed ID: 19432927
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Using a minigene approach to characterize a novel splice site mutation in human F7 gene causing inherited factor VII deficiency in a Chinese pedigree.
Yu T; Wang X; Ding Q; Fu Q; Dai J; Lu Y; Xi X; Wang H
Haemophilia; 2009 Nov; 15(6):1262-6. PubMed ID: 19601987
[TBL] [Abstract][Full Text] [Related]
19. [Molecular analysis of two pedigrees with inherited coagulation factor VII deficiency].
Liang WL; Wei HY; Lin FQ; Zhou JL
Zhonghua Er Ke Za Zhi; 2012 Nov; 50(11):817-20. PubMed ID: 23302610
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]
