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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 36401403)

  • 1. A low-dose therapy of fibrinogen supplement during perioperative period of total knee arthroplasty in an asymptomatic man with congenital dysfibrinogenemia: A case report.
    Meng D; Zhang R; Ji C; Gao S; Wang J
    Medicine (Baltimore); 2022 Nov; 101(46):e31644. PubMed ID: 36401403
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Management of dysfibrinogenemia in pregnancy: A case report.
    Yan J; Deng D; Cheng P; Liao L; Luo M; Lin F
    J Clin Lab Anal; 2018 Mar; 32(3):. PubMed ID: 28948631
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Pedigree Analysis and Diagnosis of Congenital Dysfibrinogenemia: A Case Report].
    Luo J; Duan SR; Wang H
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2022 Jan; 53(1):171-174. PubMed ID: 35048620
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Misdiagnosis of a patient with congenital dysfibrinogenemia: A case report and literature review.
    Chen X; Yan J; Xiang L; Lin F
    J Clin Lab Anal; 2022 Sep; 36(9):e24624. PubMed ID: 35949040
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congenital dysfibrinogenemia in major surgery: A description of four cases and review of the literature.
    Yan J; Luo M; Xiang L; Wu Y; Lin F
    Clin Chim Acta; 2022 Mar; 528():1-5. PubMed ID: 35063457
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Three cases of congenital dysfibrinogenemia in unrelated Chinese families: heterozygous missense mutation in fibrinogen alpha chain Argl6His.
    Luo M; Deng D; Xiang L; Cheng P; Liao L; Deng X; Yan J; Lin F
    Medicine (Baltimore); 2016 Sep; 95(39):e4864. PubMed ID: 27684817
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel mutation in the fibrinogen Aα chain (Gly13Arg, fibrinogen Nanning) causes congenital dysfibrinogenemia associated with defective peptide A release.
    Yan J; Luo M; Cheng P; Liao L; Deng X; Deng D; Lin F
    Int J Hematol; 2017 Apr; 105(4):506-514. PubMed ID: 27933517
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Diagnosis of congenital fibrinogen disorders.
    Lebreton A; Casini A
    Ann Biol Clin (Paris); 2016 Aug; 74(4):405-12. PubMed ID: 27492693
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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; 33(2):160-3. PubMed ID: 27060305
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Two novel mutations in the fibrinogen γ nodule.
    Kotlín R; Pastva O; Stikarová J; Hlaváčková A; Suttnar J; Chrastinová L; Riedel T; Salaj P; Dyr JE
    Thromb Res; 2014 Oct; 134(4):901-8. PubMed ID: 25074738
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fibrinogen Baltimore IV: congenital dysfibrinogenemia with delayed fibrin monomer polymerization.
    Ebert RF; Bell WR
    Thromb Res; 1985 Apr; 38(2):121-8. PubMed ID: 4002201
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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; 36(9):901-904. PubMed ID: 31515786
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Whole Blood Thromboelastometry by ROTEM and Thrombin Generation by Genesia According to the Genotype and Clinical Phenotype in Congenital Fibrinogen Disorders.
    Szanto T; Lassila R; Lemponen M; Lehtinen E; Neerman-Arbez M; Casini A
    Int J Mol Sci; 2021 Feb; 22(5):. PubMed ID: 33668986
    [TBL] [Abstract][Full Text] [Related]  

  • 15. One Hundred Years of Congenital Fibrinogen Disorders.
    Casini A; Moerloose P; Neerman-Arbez M
    Semin Thromb Hemost; 2022 Nov; 48(8):880-888. PubMed ID: 36055263
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dysfibrinogenemia in childhood: two cases of congenital dysfibrinogens.
    Kotlín R; Blažek B; Suttnar J; Malý M; Kvasnička J; Dyr JE
    Blood Coagul Fibrinolysis; 2010 Oct; 21(7):640-8. PubMed ID: 20829681
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dysfibrinogenemia in a patient undergoing artificial abortion after misdiagnosis and review of the literature.
    Yan J; Deng D; Luo M; Cheng P; Chi B; Yuan Y; Liao L; Lin F
    Clin Chim Acta; 2015 Jul; 447():86-9. PubMed ID: 26057201
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Thrombosis-associated hypofibrinogenemia: novel abnormal fibrinogen variant FGG c.8G>A with oxidative posttranslational modifications.
    Ceznerová E; Kaufmanová J; Stikarová J; Pastva O; Loužil J; Chrastinová L; Suttnar J; Kotlín R; Dyr JE
    Blood Coagul Fibrinolysis; 2022 Jun; 33(4):228-237. PubMed ID: 35067535
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 143():11-6. PubMed ID: 27164460
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Fibrinogen Alès: a homozygous case of dysfibrinogenemia (gamma-Asp(330)-->Val) characterized by a defective fibrin polymerization site "a".
    Lounes KC; Soria C; Mirshahi SS; Desvignes P; Mirshahi M; Bertrand O; Bonnet P; Koopman J; Soria J
    Blood; 2000 Nov; 96(10):3473-9. PubMed ID: 11071644
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.