117 related articles for article (PubMed ID: 11167768)
1. A novel two base pair deletion in the factor V gene associated with severe factor V deficiency.
Montefusco MC; Duga S; Asselta R; Santagostino E; Mancuso G; Malcovati M; Mannucci PM; Tenchini ML
Br J Haematol; 2000 Dec; 111(4):1240-6. PubMed ID: 11167768
[TBL] [Abstract][Full Text] [Related]
2. Severe coagulation factor V deficiency caused by a 4 bp deletion in the factor V gene.
Guasch JF; Cannegieter S; Reitsma PH; van't Veer-Korthof ET; Bertina RM
Br J Haematol; 1998 Apr; 101(1):32-9. PubMed ID: 9576178
[TBL] [Abstract][Full Text] [Related]
3. Severe coagulation factor V deficiency caused by 2 novel frameshift mutations: 2952delT in exon 13 and 5493insG in exon 16 of factor 5 gene.
Ajzner E E; Balogh I; Szabó T; Marosi A; Haramura G; Muszbek L
Blood; 2002 Jan; 99(2):702-5. PubMed ID: 11781258
[TBL] [Abstract][Full Text] [Related]
4. Coexistence of a novel homozygous nonsense mutation in exon 13 of the factor V gene with the homozygous Leiden mutation in two unrelated patients with severe factor V deficiency.
van Wijk R; Montefusco MC; Duga S; Asselta R; van Solinge W; Malcovati M; Tenchini ML; Mannucci PM
Br J Haematol; 2001 Sep; 114(4):871-4. PubMed ID: 11564077
[TBL] [Abstract][Full Text] [Related]
5. Five novel mutations in the gene for human blood coagulation factor V associated with type I factor V deficiency.
van Wijk R; Nieuwenhuis K; van den Berg M; Huizinga EG; van der Meijden BB; Kraaijenhagen RJ; van Solinge WW
Blood; 2001 Jul; 98(2):358-67. PubMed ID: 11435304
[TBL] [Abstract][Full Text] [Related]
6. A case of coagulation factor V deficiency caused by compound heterozygous mutations in the factor V gene.
Yamakage N; Ikejiri M; Okumura K; Takagi A; Murate T; Matushita T; Naoe T; Yamamoto K; Takamatsu J; Yamazaki T; Hamaguchi M; Kojima T
Haemophilia; 2006 Mar; 12(2):172-8. PubMed ID: 16476093
[TBL] [Abstract][Full Text] [Related]
7. [A novel mutation causes congenital factor V deficiency].
Hou LH; Xie F; Liu XE; Zhang L; Guo YL; Dong CX; Li ZT; Yang B; Yang LH
Zhonghua Xue Ye Xue Za Zhi; 2003 Sep; 24(9):455-9. PubMed ID: 14575586
[TBL] [Abstract][Full Text] [Related]
8. Severe factor V deficiency: exon skipping in the factor V gene causing a partial deletion of the C1 domain.
Asselta R; Montefusco MC; Duga S; Malcovati M; Peyvandi F; Mannucci PM; Tenchini ML
J Thromb Haemost; 2003 Jun; 1(6):1237-44. PubMed ID: 12871325
[TBL] [Abstract][Full Text] [Related]
9. Familial coagulation factor V deficiency caused by a novel 4 base pair insertion in the factor V gene: factor V Stanford.
Zehnder JL; Hiraki DD; Jones CD; Gross N; Grumet FC
Thromb Haemost; 1999 Sep; 82(3):1097-9. PubMed ID: 10494770
[TBL] [Abstract][Full Text] [Related]
10. [Severe hereditary coagulation factor V deficiency caused by two novel heterozygous mutations].
Zhou RF; Fu QH; Xu XC; Wang WB; Wu WM; Ding QL; Xie S; Zhai ZM; Hu YQ; Wang XF; Wu JS; Wang HL
Zhonghua Xue Ye Xue Za Zhi; 2005 Mar; 26(3):129-32. PubMed ID: 15946520
[TBL] [Abstract][Full Text] [Related]
11. Homozygous factor V splice site mutation associated with severe factor V deficiency.
Schrijver I; Koerper MA; Jones CD; Zehnder JL
Blood; 2002 Apr; 99(8):3063-5. PubMed ID: 11929802
[TBL] [Abstract][Full Text] [Related]
12. Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern.
Dall'Osso C; Guella I; Duga S; Locatelli N; Paraboschi EM; Spreafico M; Afrasiabi A; Pechlaner C; Peyvandi F; Tenchini ML; Asselta R
Haematologica; 2008 Oct; 93(10):1505-13. PubMed ID: 18728029
[TBL] [Abstract][Full Text] [Related]
13. Identification of three F5 gene mutations associated with inherited coagulation factor V deficiency in two Chinese pedigrees.
Fu QH; Zhou RF; Liu LG; Wang WB; Wu WM; Ding QL; Hu YQ; Wang XF; Wang ZY; Wang HL
Haemophilia; 2004 May; 10(3):264-70. PubMed ID: 15086325
[TBL] [Abstract][Full Text] [Related]
14. Homozygous F5 deep-intronic splicing mutation resulting in severe factor V deficiency and undetectable thrombin generation in platelet-rich plasma.
Castoldi E; Duckers C; Radu C; Spiezia L; Rossetto V; Tagariello G; Rosing J; Simioni P
J Thromb Haemost; 2011 May; 9(5):959-68. PubMed ID: 21320286
[TBL] [Abstract][Full Text] [Related]
15. Molecular characterisation of Tyr530Ser and IVS16-1G>T mutations causing severe factor V deficiency.
Zheng W; Liu Y; Luo Y; Chen Z; Wang Y; Zhang L; Gao G; Yao Z
Thromb Haemost; 2010 Sep; 104(3):536-43. PubMed ID: 20664902
[TBL] [Abstract][Full Text] [Related]
16. Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency.
Paraboschi EM; Kayiran SM; Özbek N; Gürakan B; Peyvandi F; Guella I; Duga S; Asselta R
Haemophilia; 2012 Mar; 18(2):205-10. PubMed ID: 21777354
[TBL] [Abstract][Full Text] [Related]
17. Gene analysis and prenatal diagnosis for two families of congenital factor V deficiency.
Cao L; Wang Z; Li H; Wang W; Zhao X; Zhang W; Ding J; Ruan C
Haemophilia; 2011 Jan; 17(1):65-9. PubMed ID: 20722745
[TBL] [Abstract][Full Text] [Related]
18. Molecular characterization of 11 novel mutations in patients with heterozygous and homozygous FV deficiency.
Cutler JA; Patel R; Rangarajan S; Tait RC; Mitchell MJ
Haemophilia; 2010 Nov; 16(6):937-42. PubMed ID: 20546033
[TBL] [Abstract][Full Text] [Related]
19. Molecular characterization of 3 factor V mutations, R2174L, V1813M, and a 5-bp deletion, that cause factor V deficiency.
Shinozawa K; Amano K; Suzuki T; Tanaka A; Iijima K; Takahashi H; Inaba H; Fukutake K
Int J Hematol; 2007 Dec; 86(5):407-13. PubMed ID: 18192108
[TBL] [Abstract][Full Text] [Related]
20. Type I coagulation factor V deficiency caused by compound heterozygous mutation of F5 gene.
Fu Q; Wu W; Ding Q; Hu Y; Wang X; Wang H; Wang Z
Haemophilia; 2003 Sep; 9(5):646-9. PubMed ID: 14511309
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
