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Journal Abstract Search

557 related items for PubMed ID: 28164683

  • 1.
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  • 2. [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
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  • 3. [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
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  • 5. Congenital combined deficiency of factor VII and X in a patient due to accidental diphacinone intoxication.
    Zheng F, Jin Y, Wang M, Niu Z, Xu P, Xie H.
    Thromb Haemost; 2011 Jul; 106(1):180-1. PubMed ID: 21544315
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  • 6. Analysis of Phenotype and Genotypein an Inherited Coagulation Factor VII Deficiency Pedigree.
    Li M, Jin Y, Wang M, Ding H.
    Clin Lab; 2019 Dec 01; 65(12):. PubMed ID: 31850724
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  • 7. [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 01; 33(3):296-9. PubMed ID: 27264807
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  • 9. [Molecular analysis of two pedigrees with inherited coagulation factor VII deficiency].
    Liang WL, Wei HY, Lin FQ, Zhou JL.
    Zhonghua Er Ke Za Zhi; 2012 Nov 01; 50(11):817-20. PubMed ID: 23302610
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  • 10. [Genotypic and phenotypic analysis of a case with inherited coagulation factor X deficiency].
    Chen T, Li F, Shu K, Liu J, Shen C, Zhang Z, Jin S, Wang X, Jiang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Aug 10; 35(4):544-547. PubMed ID: 30098253
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  • 12. [Molecular genetics and clinical features of nine patients with inherited coagulation factor VII deficiency].
    Jin YH, Wang MS, Zheng FX, Xie YS, Xie HX, Xu PF.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug 10; 29(4):404-7. PubMed ID: 22875495
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  • 13. [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 10; 25(9):519-22. PubMed ID: 15569527
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  • 14. Japanese family with congenital factor VII deficiency.
    Sakakibara K, Okayama Y, Fukushima K, Kaji S, Muraoka M, Arao Y, Shimada A.
    Pediatr Int; 2015 Oct 10; 57(5):1023-4. PubMed ID: 26310716
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  • 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 10; 22(8):673-9. PubMed ID: 22008904
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  • 20. Pharmacokinetic properties of recombinant FVIIa in inherited FVII deficiency account for a large volume of distribution at steady state and a prolonged pharmacodynamic effect.
    Morfini M, Batorova A, Mariani G, Auerswald G, Bernardi F, Di Minno G, Dolce A, Fede C, Giansily-Blaizot M, Ingerslev J, Martinowitz U, Napolitano M, Pinotti M, Schved JF, International FVII [IF7] and Seven Treatment Evaluation Registry [STER] Study Groups.
    Thromb Haemost; 2014 Aug 10; 112(2):424-5. PubMed ID: 24763923
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