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 *

155 related articles for article (PubMed ID: 35417978)

  • 1. An unanticipated prolonged baseline ACT during cardiac surgery due to factor XII deficiency.
    L Apostel HJC; De Bie B; Kats S; Schreiber JU
    Ann Card Anaesth; 2022; 25(2):229-232. PubMed ID: 35417978
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Standard Point-of-Care Hemochron Jr. ACT+ Test in Monitoring Heparin Administration for Cardiopulmonary Bypass in Severe Factor XII Deficiency.
    Erkinaro T; Moilanen J; Lahtinen J; Mosorin M; Savolainen ER
    J Cardiothorac Vasc Anesth; 2022 Jul; 36(7):2031-2034. PubMed ID: 34130893
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cardiopulmonary bypass in a child with severe Factor XII deficiency.
    Shrimpton N; Patukale A; Rane M; Barbaro P; Alphonso N; Venugopal P
    Perfusion; 2022 Apr; 37(3):316-320. PubMed ID: 33663270
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Homozygous missense variant F12 (Gly506Asp) associated with severe factor XII deficiency: a case report.
    Aljabry M; Algazlan A; Alsubaie N; Dher SB; Aljabri HS; Alotaibi GS
    J Med Case Rep; 2023 Dec; 17(1):504. PubMed ID: 38057855
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Are we to pay attention to factor XII deficiency?].
    Remková A; Remko M
    Vnitr Lek; 2015 Dec; 61(12 Suppl 5):5S63-6. PubMed ID: 27124975
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Evaluation of thromboelastography in two factor XII-deficient cats.
    Blois SL; Holowaychuk MK; Wood RD
    JFMS Open Rep; 2015; 1(1):2055116915585025. PubMed ID: 28491358
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel homozygous missense mutation (Met527Ile) in a consanguineous marriage family with inherited factor XII deficiency.
    Liu M; Wang H; Lin M; Jin Y; Yang L; Wang M
    Hematology; 2020 Dec; 25(1):502-506. PubMed ID: 33317433
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel factor XII mutation, FXII R84P, causing factor XII deficiency in a patient with hereditary spastic paraplegia.
    Matsuki E; Miyakawa Y; Okamoto S
    Blood Coagul Fibrinolysis; 2011 Apr; 22(3):227-30. PubMed ID: 21297451
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Factor XII (Hageman Factor) Deficiency: a rare harbinger of life threatening complications.
    Chaudhry LA; El-Sadek WYM; Chaudhry GA; Al-Atawi FE
    Pan Afr Med J; 2019; 33():39. PubMed ID: 31384354
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular genetic analysis of Korean patients with coagulation factor XII deficiency.
    Kwon MJ; Kim HJ; Lee KO; Jung CW; Kim SH
    Blood Coagul Fibrinolysis; 2010 Jun; 21(4):308-12. PubMed ID: 20386432
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Is factor XII deficiency related to recurrent miscarriage?
    Matsuura T; Kobayashi T; Asahina T; Kanayama N; Terao T
    Semin Thromb Hemost; 2001; 27(2):115-20. PubMed ID: 11372764
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Global cerebral infarction after aortic arch replacement surgery in a patient with postoperatively revealed factor XII deficiency: a case report.
    Yoshida K; Tanaka S; Sato Y; Watanabe K; Muramatsu K; Murakawa M
    J Med Case Rep; 2020 Sep; 14(1):150. PubMed ID: 32912328
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel deleterious mutation in the F12 gene in a Korean family with severe coagulation factor XII deficiency.
    Kim HJ; Kim HJ; Kwon EH; Lee KO; Park IA; Kim SH
    Blood Coagul Fibrinolysis; 2010 Oct; 21(7):683-6. PubMed ID: 20729721
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Genetic analysis of a Chinese pedigree affected with Congenital coagulation factor XII deficiency due to a c.1A>G start codon variant of F12 gene].
    Ji W; Lin S; Chen J; Jin C; Lin X; Ye Z; Qiu L; Qian D
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 May; 40(5):547-551. PubMed ID: 37102287
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Incidence of factor XII deficiency in critically ill patients with a prolonged activated partial thromboplastin time: a prospective observational study.
    Mishra L; Lee D; Ho KM
    Blood Coagul Fibrinolysis; 2023 Sep; 34(6):364-369. PubMed ID: 37395184
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Analysis of a consanguineous pedigree affected with hereditary coagulation factor XII deficiency caused by homozygous Gly341Arg mutation].
    Yang L; Jin S; Ji W; Cheng X; Li X; Jin Y; Wang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Feb; 35(1):69-73. PubMed ID: 29419864
    [TBL] [Abstract][Full Text] [Related]  

  • 17. "Familial Multiple Coagulation Factor Deficiencies of FXI and FXII in an Asymptomatic Saudi Woman".
    Al-Ansari RY; Alruwaili AF; Alqahtani KM; Al-Harbi AF; Woodman A
    J Investig Med High Impact Case Rep; 2023; 11():23247096231199413. PubMed ID: 37705386
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Compound heterozygous mutations Glu502Lys and Met527Thr of the FXII gene in a patient with factor XII deficiency.
    Zhang H; Liu S; Lin C; Luo S; Yang L; Jin Y; Zhu L; Wang M
    Hematology; 2019 Dec; 24(1):420-425. PubMed ID: 30929639
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Identification of a novel mutation of factor XII gene in a family with coagulation FXII deficiency].
    Xie H; Lv M; Yang X; Zhu L; Yang L; Jin Y; Wang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Jun; 30(3):313-7. PubMed ID: 23744322
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of congenital factor XII deficiency in Taiwanese patients: identification of one novel and one common mutation.
    Chou SC; Lin CY; Lin HY; Pai CH; Yu CY; Kuo SF; Lin JS; Lin PT; Hung MH; Hsieh HN; Liu HC; Shen MC
    Int J Hematol; 2022 Oct; 116(4):528-533. PubMed ID: 35675023
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.