212 related articles for article (PubMed ID: 10494770)
1. 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]
2. Familial coagulation factor V deficiency caused by a novel 4 base pair insertion in the factor V gene: factor V Stanford [erratum].
Zehnder JL; Hiraki DD; Jones CD; Gross N; Grumet FC
Thromb Haemost; 1999 Nov; 82(5):XII. PubMed ID: 10681265
[No Abstract] [Full Text] [Related]
3. [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]
4. [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]
5. [Identification of two novel mutations of human blood coagulation factor V gene in a Chinese family with congenital factor V deficiency].
Zheng WD; Liu YH; Liu HF; Chen ZH; Wang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Oct; 23(5):515-8. PubMed ID: 17029198
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. [Two novel factor V gene mutations associated with congenital coagulation factor V deficiency, study of one pedigree].
Fu QH; Wang HL; Wang MS; Ding QL; Wu WM; Hu YQ; Wang XF; Wang ZY
Zhonghua Yi Xue Za Zhi; 2003 Feb; 83(4):312-5. PubMed ID: 12812650
[TBL] [Abstract][Full Text] [Related]
9. [Identification of a novel mutation of human blood coagulation FV gene associated with congenital FV deficiency].
Fu WJ; Hou J; Wang DX; Yu RQ
Zhonghua Xue Ye Xue Za Zhi; 2003 Mar; 24(3):119-21. PubMed ID: 12697120
[TBL] [Abstract][Full Text] [Related]
10. Phenotyping and genotyping of coagulation factor V Leiden.
Engel H; Zwang L; van Vliet HH; Michiels JJ; Stibbe J; Lindemans J
Thromb Haemost; 1996 Feb; 75(2):267-9. PubMed ID: 8815574
[TBL] [Abstract][Full Text] [Related]
11. Identification of the first Alu-mediated large deletion involving the F5 gene in a compound heterozygous patient with severe factor V deficiency.
Guella I; Paraboschi EM; van Schalkwyk WA; Asselta R; Duga S
Thromb Haemost; 2011 Aug; 106(2):296-303. PubMed ID: 21614419
[TBL] [Abstract][Full Text] [Related]
12. Concerns about the mutations identified in a case of familial coagulation factor V deficiency: factor V Stanford.
Montefusco MC; Asselta R; van Wijk R; Duga S; Tenchini ML
Thromb Haemost; 2000 Dec; 84(6):1131-2. PubMed ID: 11154134
[No Abstract] [Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. [New allele-specific primers for detection of Leiden mutation in exon 10 of factor V gene in thrombophilias].
Zykova ES; Patrushev LI; Kaiushin AL; Korosteleva MD; Miroshnikov AI; Bokarev IN; Leont'ev SG; Koshkin VM; Severin ES
Bioorg Khim; 1997 Mar; 23(3):205-10. PubMed ID: 9190792
[TBL] [Abstract][Full Text] [Related]
17. Profound dihydropyrimidine dehydrogenase deficiency resulting from a novel compound heterozygote genotype.
Johnson MR; Wang K; Diasio RB
Clin Cancer Res; 2002 Mar; 8(3):768-74. PubMed ID: 11895907
[TBL] [Abstract][Full Text] [Related]
18. [Gene analysis of five inherited factor V deficiency cases].
Cao LJ; Wang ZY; Su YH; Yang HY; Zhao XJ; Zhang W; Yu ZQ; Bai X; Ruan CG
Zhonghua Xue Ye Xue Za Zhi; 2008 Mar; 29(3):145-8. PubMed ID: 18788609
[TBL] [Abstract][Full Text] [Related]
19. Discrimination between normal wildtype and carriers of coagulation factor V Leiden mutation by the activated protein C resistance test in the presence of factor V deficient plasma.
Reuner KH; Litfin F; Patscheke H
Eur J Clin Chem Clin Biochem; 1997 Jan; 35(1):41-5. PubMed ID: 9156566
[TBL] [Abstract][Full Text] [Related]
20. Factor V Leiden genotyping using real-time fluorescent polymerase chain reaction.
Sanders Sevall J
Mol Cell Probes; 2000 Aug; 14(4):249-53. PubMed ID: 10970729
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
