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 *

168 related articles for article (PubMed ID: 25153695)

  • 1. Evaluation of GenoFlow Thrombophilia Array Test Kit in its detection of mutations in Factor V Leiden (G1691A), prothrombin G20210A, MTHFR C677T and A1298C in blood samples from 113 Turkish female patients.
    Aytekin E; Ergun SG; Ergun MA; Percin FE
    Genet Test Mol Biomarkers; 2014 Nov; 18(11):717-21. PubMed ID: 25153695
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Factor V Leiden G1691A, prothrombin G20210A, and MTHFR C677T mutations in Turkish inflammatory bowel disease patients.
    Yasa MH; Bolaman Z; Yukselen V; Kadikoylu G; Karaoglul AO; Batun S
    Hepatogastroenterology; 2007; 54(77):1438-42. PubMed ID: 17708272
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The frequency of factor V Leiden and concomitance of factor V Leiden with prothrombin G20210A mutation and methylene tetrahydrofolate reductase C677T gene mutation in healthy population of Denizli, Aegean region of Turkey.
    Kabukcu S; Keskin N; Keskin A; Atalay E
    Clin Appl Thromb Hemost; 2007 Apr; 13(2):166-71. PubMed ID: 17456626
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Risk Factors of Thrombophilia-Related Mutations for Early and Late Pregnancy Loss.
    Borsi E; Potre O; Ionita I; Samfireag M; Secosan C; Potre C
    Medicina (Kaunas); 2024 Mar; 60(4):. PubMed ID: 38674167
    [No Abstract]   [Full Text] [Related]  

  • 5. Primary thrombophilia in Mexico. II. Factor V G1691A (Leiden), prothrombin G20210A, and methylenetetrahydrofolate reductase C677T polymorphism in thrombophilic Mexican mestizos.
    Ruiz-Argüelles GJ; Garcés-Eisele J; Reyes-Núñez V; Ramírez-Cisneros FJ
    Am J Hematol; 2001 Jan; 66(1):28-31. PubMed ID: 11426488
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations are not associated with chronic limb ischemia: the Linz Peripheral Arterial Disease (LIPAD) study.
    Mueller T; Marschon R; Dieplinger B; Haidinger D; Gegenhuber A; Poelz W; Webersinke G; Haltmayer M
    J Vasc Surg; 2005 May; 41(5):808-15. PubMed ID: 15886665
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inherited thrombophilia with recurrent pregnancy loss in Turkish women--a real phenomenon?
    Yildiz G; Yavuzcan A; Yildiz P; Süer N; Tandoğan N
    Ginekol Pol; 2012 Aug; 83(8):598-603. PubMed ID: 23342883
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Inherited Thrombophilia in a Lebanese Family of Four Generations: A Case Report of Recurrent Miscarriage.
    Khalife S; Bissar-Tadmouri N
    Vasc Health Risk Manag; 2020; 16():53-56. PubMed ID: 32021228
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran.
    Rahimi Z; Nomani H; Mozafari H; Vaisi-Raygani A; Madani H; Malek-Khosravi S; Parsian A
    Blood Coagul Fibrinolysis; 2009 Jun; 20(4):252-6. PubMed ID: 19349859
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Factor V Leiden G1691A, Prothrombin G20210A, and MTHFR C677T and A1298C Mutations in Patients With Sickle Cell Disease in Tunisia.
    Belhaj Nefissi R; Doggui R; Ouali F; Messaoud T; Gritli N
    Hemoglobin; 2018 Mar; 42(2):96-102. PubMed ID: 30200836
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evaluation of Factor V Leiden, Prothrombin G20210A, MTHFR C677T and MTHFR A1298C gene polymorphisms in retinopathy of prematurity in a Turkish cohort.
    Aydin H; Gunay M; Celik G; Gunay BO; Aydin UT; Karaman A
    Ophthalmic Genet; 2016 Dec; 37(4):415-418. PubMed ID: 27018927
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prevalence of factor V Leiden G1691A, MTHFR C677T, and prothrombin G20210A among Asian Indian sickle cell patients.
    Pandey SK; Meena A; Kishor K; Mishra RM; Pandey S; Saxena R
    Clin Appl Thromb Hemost; 2012 Jun; 18(3):320-3. PubMed ID: 22084413
    [TBL] [Abstract][Full Text] [Related]  

  • 13. MTHFR (C677T, A1298C), FV Leiden polymorphisms, and the prothrombin G20210A mutation in arterial ischemic stroke among young tunisian adults.
    M'barek L; Sakka S; Meghdiche F; Turki D; Maalla K; Dammak M; Kallel C; Mhiri C
    Metab Brain Dis; 2021 Mar; 36(3):421-428. PubMed ID: 33400068
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The association of factor V G1961A (factor V Leiden), prothrombin G20210A, MTHFR C677T and PAI-1 4G/5G polymorphisms with recurrent pregnancy loss in Bosnian women.
    Jusić A; Balić D; Avdić A; Pođanin M; Balić A
    Med Glas (Zenica); 2018 Aug; 15(2):158-163. PubMed ID: 29703881
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evaluation of Factor V G1691A, prothrombin G20210A, Factor XIII V34L, MTHFR A1298C, MTHFR C677T and PAI-1 4G/5G genotype frequencies of patients subjected to cardiovascular disease (CVD) panel in south-east region of Turkey.
    Oztuzcu S; Ergun S; Ulaşlı M; Nacarkahya G; Iğci YZ; Iğci M; Bayraktar R; Tamer A; Çakmak EA; Arslan A
    Mol Biol Rep; 2014 Jun; 41(6):3671-6. PubMed ID: 24532105
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Effects of inherited thrombophilia in women with recurrent pregnancy loss.
    Habibovic Z; Zeybek B; Sanhal C; Eroglu Z; Karaca E; Ulukus M
    Clin Exp Obstet Gynecol; 2011; 38(4):347-50. PubMed ID: 22268272
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Role of Factor V Leiden, Prothrombin G20210A, and MTHFR C677T Mutations in Neonatal Cerebral Sinovenous Thrombosis.
    Garrido-Barbero M; Arnaez J; Loureiro B; Arca G; Agut T; Garcia-Alix A
    Clin Appl Thromb Hemost; 2019; 25():1076029619834352. PubMed ID: 31025572
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis.
    Almawi WY; Tamim H; Kreidy R; Timson G; Rahal E; Nabulsi M; Finan RR; Irani-Hakime N
    J Thromb Thrombolysis; 2005 Jun; 19(3):189-96. PubMed ID: 16082606
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians.
    Eid SS; Rihani G
    Clin Lab Sci; 2004; 17(4):200-2. PubMed ID: 15559724
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association between FVL G1691A, FII G20210A, and MTHFR C677T and A1298C polymorphisms and Turkish women with recurrent pregnancy loss.
    Yengel I; Yorulmaz T; Api M
    Med Glas (Zenica); 2020 Feb; 17(1):129-135. PubMed ID: 31994856
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.