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311 related items for PubMed ID: 15569527

  • 1. [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
    [Abstract] [Full Text] [Related]

  • 2. Molecular characterization of two novel mutations causing factor X deficiency in a Chinese pedigree.
    Wang WB, Fu QH, Zhou RF, Wu WM, Ding QL, Hu YQ, Wang XF, Wang HL, Wang ZY.
    Haemophilia; 2005 Jan; 11(1):31-7. PubMed ID: 15660986
    [Abstract] [Full Text] [Related]

  • 3. [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
    [Abstract] [Full Text] [Related]

  • 4. [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]

  • 5. [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 25; 26(3):129-32. PubMed ID: 15946520
    [Abstract] [Full Text] [Related]

  • 6. [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 25; 24(9):449-51. PubMed ID: 14575584
    [Abstract] [Full Text] [Related]

  • 7. Analysis of the novel factor X gene mutation Glu51Lys in two families with factor X-Riyadh anomaly.
    Al-Hilali A, Wulff K, Abdel-Razeq H, Saud KA, Al-Gaili F, Herrmann FH.
    Thromb Haemost; 2007 Apr 25; 97(4):542-5. PubMed ID: 17393015
    [Abstract] [Full Text] [Related]

  • 8. Molecular defects in the factor X gene caused by novel heterozygous mutations IVS5+1G>A and Asp409del.
    Zhou JW, Liang Q, Chen Q, Xie Y, Ding QL, Wang XF, Xi XD, Wang HL.
    Haemophilia; 2013 Jan 25; 19(1):94-9. PubMed ID: 22931370
    [Abstract] [Full Text] [Related]

  • 9. [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 25; 31(1):16-20. PubMed ID: 24510554
    [Abstract] [Full Text] [Related]

  • 10. [Homozygous missense mutation p.Val298Met of F10 gene causing hereditary coagulation factor X deficiency in a Chinese pedigree].
    Jin Y, Hao X, Cheng X, Yang L, Chen Y, Xie H, Wang Y, Wang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun 25; 33(3):296-9. PubMed ID: 27264807
    [Abstract] [Full Text] [Related]

  • 11. Characterization of a homozygous Gly11Val mutation in the Gla domain of coagulation factor X.
    Chafa O, Tagzirt M, Tapon-Bretaudière J, Reghis A, Fischer AM, LeBonniec BF.
    Thromb Res; 2009 May 25; 124(1):144-8. PubMed ID: 19135706
    [Abstract] [Full Text] [Related]

  • 12. [Double heterozygous mutations of non-canonical splice (IVS1a + 5g > a) and His348Gln caused inherited coagulation factor VII deficiency].
    Ding QL, Wang HL, Wang XF, Wang MS, Fu QH, Wu WM, Hu YQ, Wang ZY.
    Zhonghua Xue Ye Xue Za Zhi; 2004 Mar 25; 25(3):139-42. PubMed ID: 15182580
    [Abstract] [Full Text] [Related]

  • 13. The impact of Glu102Lys on the factor X function in a patient with a doubly homozygous factor X deficiency (Gla14Lys and Glu102Lys).
    Forberg E, Huhmann I, Jimenez-Boj E, Watzke HH.
    Thromb Haemost; 2000 Feb 25; 83(2):234-8. PubMed ID: 10739379
    [Abstract] [Full Text] [Related]

  • 14. Factor X deficiency.
    Menegatti M, Peyvandi F.
    Semin Thromb Hemost; 2009 Jun 25; 35(4):407-15. PubMed ID: 19598069
    [Abstract] [Full Text] [Related]

  • 15. Severe factor X deficiency in three unrelated Palestinian patients is caused by homozygosity for the mutation c302delG-correlation with thrombin generation and thromboelastometry.
    Livnat T, Shenkman B, Kenet G, Tamarin I, Gillis S, Varon D, Iijima K, Zivelin A, Salomon O.
    Blood Coagul Fibrinolysis; 2011 Dec 25; 22(8):673-9. PubMed ID: 22008904
    [Abstract] [Full Text] [Related]

  • 16. [Clotting factor X deficiency resulted from an T 58-->G mutation within exon 1 of human factor X gene].
    Yin J, Wang H, Wang X.
    Zhonghua Xue Ye Xue Za Zhi; 2001 Sep 25; 22(9):481-3. PubMed ID: 11758231
    [Abstract] [Full Text] [Related]

  • 17. Reduced activation of the Gla19Ala FX variant via the extrinsic coagulation pathway results in symptomatic CRMred FX deficiency.
    Pinotti M, Marchetti G, Baroni M, Cinotti F, Morfini M, Bernardi F.
    Thromb Haemost; 2002 Aug 25; 88(2):236-41. PubMed ID: 12195695
    [Abstract] [Full Text] [Related]

  • 18. [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]

  • 19. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 25; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 20. [Hereditary hemorrhagic telangiectasia resulted from a nonsense mutation Arg479 Stop in the ALK-1 gene].
    Xie BS, Xie S, Chen P, Zhu MY, Zheng JY, Wang XF, Fu QH, Zhou RF, Wang WB, Wu WM, Ding QL, Wang HL, Hu LM.
    Zhonghua Xue Ye Xue Za Zhi; 2004 Sep 25; 25(9):536-9. PubMed ID: 15569532
    [Abstract] [Full Text] [Related]

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