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

214 related items for PubMed ID: 24844956

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. [Inherited dysfibrinogenemia caused by Arg275His in the beta chain of fibrinogen].
    Fang Y, Wang X, Qi H, Wu W, Ding Q, Dai J, Zhou R, Wang W, Xie S, Wang H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr; 22(2):201-3. PubMed ID: 15793786
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. [Inherited dysfibrinogenemia caused by Arg16His mutation in alpha chain of fibrinogen.].
    Zhao XJ, Wang ZY, Jiang MH, Zhang W, Cao LJ, Ma ZN, Dong NZ, Bai X, Yu ZQ, Ruan CG.
    Zhonghua Xue Ye Xue Za Zhi; 2010 Mar; 31(3):154-6. PubMed ID: 20510102
    [Abstract] [Full Text] [Related]

  • 6. [Genetic Analysis of A Case of Congenital Dysfibrinogenemia Caused by Arg16His Mutation in Exon 2 of FGA].
    Zhang YL, Liu SY, Zhang ZL, Tao XY, Peng XX, Kong YY.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2017 Oct; 25(5):1514-1517. PubMed ID: 29070135
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. [Analysis of a pedigree affected with congenital dysfibrinogenemia due to a novel Gly31Glu mutation of FGA gene].
    Wang X, Yang X, Yang W, Shu K, Li F, Liu J, Zhang Z, Li S, Jiang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Sep 10; 36(9):901-904. PubMed ID: 31515786
    [Abstract] [Full Text] [Related]

  • 9. [Genetic analysis of an inherited afibrinogenemia family caused by a novel frameshift mutation in FGA].
    Xue F, Ge J, Gu DS, DU WT, Sui T, Zhao HF, Zhang L, Yang RC.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2009 Aug 10; 17(4):1021-5. PubMed ID: 19698251
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. [Analysis of a family with congenital dysfibrinogenemia caused by an Arg275His mutation in the gamma chain of fibrinogen].
    Yan J, Deng D, Deng X, Luo M, Cheng P, Liao L, Lin F.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr 10; 33(2):160-3. PubMed ID: 27060305
    [Abstract] [Full Text] [Related]

  • 14. [A Family with Congenital Dysfibrinogenemia and Blood Transfusion].
    Liao XC, Zhang SS, Yang ZJ, Zhu CL, Huang HN, Luo RX, Li SN, Xie HQ, Li HL, Mo ZN.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2023 Oct 10; 31(5):1469-1474. PubMed ID: 37846702
    [Abstract] [Full Text] [Related]

  • 15. [Congenital Fibrinogen Deficiency Caused by Novel FGG Gene Mutation].
    Wang TT, Shao JR, Wang J, Cheng Y, Zhang XQ, Fang YH, Yao CF, Zhang XS.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2021 Apr 10; 29(2):586-590. PubMed ID: 33812435
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. [Genetic analysis of a Chinese pedigree affected with Congenital dysfibrinogenemia due to variant of FGG gene].
    Shao X, Ma J, Wang Z, Sun M, Huang Z, Jiang Z, Liu X, Li S, Liu Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Nov 10; 40(11):1324-1329. PubMed ID: 37906135
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. [Phenotype and genotype analyses of two pedigrees with inherited fibrinogen deficiency].
    Jia KQ, Su ZX, Chen HL, Zheng XY, Zeng ML, Zhang K, Ye LY, Yang LL, Jin YH, Wang MS.
    Zhonghua Xue Ye Xue Za Zhi; 2023 Nov 14; 44(11):930-935. PubMed ID: 38185523
    [Abstract] [Full Text] [Related]

  • 20. Congenital afibrinogenemia: Identification and characterization of two novel homozygous fibrinogen Aα and Bβ chain mutations in two Tunisian families.
    Amri Y, Toumi Nel H, Hadj Fredj S, de Moerloose P.
    Thromb Res; 2016 Jul 14; 143():11-6. PubMed ID: 27164460
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.