531 related articles for article (PubMed ID: 15946520)
1. [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]
2. [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]
3. 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]
4. [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]
5. [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]
6. [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]
7. [Inherited coagulation factor X deficiency caused by two novel mutations in factor X gene].
Wang WB; Wang HL; Wang XF; Fu QH; Zhou RF; Xie S; Hu YQ; Wang ZY
Zhonghua Xue Ye Xue Za Zhi; 2004 Sep; 25(9):519-22. PubMed ID: 15569527
[TBL] [Abstract][Full Text] [Related]
8. [Gene analysis of a combined inherited factor VII and factor X deficiency pedigree].
Wang MS; Jin YH; Zheng FX; Xie HX; Xu PF; Niu ZZ
Zhonghua Xue Ye Xue Za Zhi; 2011 Dec; 32(12):854-7. PubMed ID: 22339961
[TBL] [Abstract][Full Text] [Related]
9. [Combined deficiency of factors V and VIII caused by a novel compound heterozygous mutation of gene Lman1].
Ge J; Xue F; Gu DS; DU WT; Zhao HF; Sui T; Li HY; Ma L; Zhang L; Yang RC
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2010 Feb; 18(1):185-90. PubMed ID: 20137144
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. 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]
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. [Analysis of a consanguineous pedigree featuring hereditary coagulation factor Ⅴ deficiency].
Xie YS; Zhang Y; Zhu LQ; Jin YH; Yang LH; Xie HX; Wang MS; Yang XL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Apr; 30(2):161-4. PubMed ID: 23568726
[TBL] [Abstract][Full Text] [Related]
14. [Prothrombin deficiency resulted from a homozygous Glu29 to Gly mutation in the prothrombin gene].
Wang WB; Wang HL; Huang CY; Fang Y; Fu QH; Zhou RF; Xie S; Ding QL; Wu WM; Wang XF; Hu YQ; Wang ZY
Zhonghua Xue Ye Xue Za Zhi; 2003 Sep; 24(9):449-51. PubMed ID: 14575584
[TBL] [Abstract][Full Text] [Related]
15. Factor 5 mutation profile in German patients with homozygous and heterozygous factor V deficiency.
Delev D; Pavlova A; Heinz S; Seifried E; Oldenburg J
Haemophilia; 2009 Sep; 15(5):1143-53. PubMed ID: 19486170
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Factor V deficiency.
Asselta R; Peyvandi F
Semin Thromb Hemost; 2009 Jun; 35(4):382-9. PubMed ID: 19598066
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Phenotype and genotype analysis for a consanguineous pedigree with combined coagulation factor VII and X deficiency].
Jin Y; Wang M; Wang Y; Yang X; Yang L; Xie Y; Xie H; Zhu L; Yu F
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):16-20. PubMed ID: 24510554
[TBL] [Abstract][Full Text] [Related]
20. Molecular characterization of a type I quantitative factor V deficiency in a thrombosis patient that is "pseudo homozygous" for activated protein C resistance.
Guasch JF; Lensen RP; Bertina RM
Thromb Haemost; 1997 Feb; 77(2):252-7. PubMed ID: 9157576
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
