These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

534 related items for 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
    [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 25; 83(4):312-5. PubMed ID: 12812650
    [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 25; 10(3):264-70. PubMed ID: 15086325
    [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 25; 23(5):515-8. PubMed ID: 17029198
    [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 25; 24(9):455-9. PubMed ID: 14575586
    [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 25; 29(3):145-8. PubMed ID: 18788609
    [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; 25(9):519-22. PubMed ID: 15569527
    [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 25; 32(12):854-7. PubMed ID: 22339961
    [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 25; 18(1):185-90. PubMed ID: 20137144
    [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 25; 24(3):119-21. PubMed ID: 12697120
    [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 25; 12(2):172-8. PubMed ID: 16476093
    [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 10; 86(2):124-7. PubMed ID: 16620721
    [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 10; 30(2):161-4. PubMed ID: 23568726
    [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 10; 24(9):449-51. PubMed ID: 14575584
    [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 10; 15(5):1143-53. PubMed ID: 19486170
    [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 10; 82(3):1097-9. PubMed ID: 10494770
    [Abstract] [Full Text] [Related]

  • 17. Factor V deficiency.
    Asselta R, Peyvandi F.
    Semin Thromb Hemost; 2009 Jun 10; 35(4):382-9. PubMed ID: 19598066
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No 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 10; 31(1):16-20. PubMed ID: 24510554
    [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 10; 77(2):252-7. PubMed ID: 9157576
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 27.