179 related articles for article (PubMed ID: 38674167)
21. Hyperbaric oxygen treatment results in a group of Turkish central retinal artery occlusion patients with a combined presence of thrombophilic mutations.
Çevik MÖ; Bagli BS; Çevik SG
Undersea Hyperb Med; 2020; 47(1):65-73. PubMed ID: 32176948
[TBL] [Abstract][Full Text] [Related]
22. [Impact of inherited thrombophilia on the development of some pregnancy complications].
Koleva R; Dimitrova V; Chernev T; Savov A; Karag'ozova Zh; Mazneŭkova V; Kremenski I
Akush Ginekol (Sofiia); 2005; 44(5):18-26. PubMed ID: 16313049
[TBL] [Abstract][Full Text] [Related]
23. Factor V Leiden, prothrombin G20210A, and methylene tetrahydrofolate reductase mutations and stillbirth: the Stillbirth Collaborative Research Network.
Silver RM; Saade GR; Thorsten V; Parker CB; Reddy UM; Drews-Botsch C; Conway D; Coustan D; Dudley DJ; Bukowski R; Rowland Hogue CJ; Pinar H; Varner MW; Goldenberg R; Willinger M
Am J Obstet Gynecol; 2016 Oct; 215(4):468.e1-468.e17. PubMed ID: 27131585
[TBL] [Abstract][Full Text] [Related]
24. CENTRAL RETINAL VEIN OCCLUSION IN OTHERWISE HEALTHY CHILDREN AND ADOLESCENTS: Association With Multigenetic Variants of Thrombophilia.
Bremond-Gignac D; Daruich A; Gallet M; Menoud PA; Nowomiejska K; Rejdak R; Behar-Cohen F; Benkhalifa M; Copin H
Retina; 2020 Jul; 40(7):1339-1343. PubMed ID: 31095065
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. [Inherited thrombophilic factors in women with secondary infertility].
Ivanov P; Gecheva S; Tsvyatkovska T; Georgieva G; Komsa-Penkova R; Konova E; Simeonova M; Tanchev S
Akush Ginekol (Sofiia); 2012; 51(4):3-7. PubMed ID: 23234018
[TBL] [Abstract][Full Text] [Related]
27. [Prevalence of thrombophilic mutations of FV Leiden, prothrombin G20210A and PAl-1 4G/5G and their combinations in a group of 1450 healthy middle-aged individuals in the Prague and Central Bohemian regions (results of FRET real-time PCR assay)].
Kvasnicka J; Hájková J; Bobcíková P; Kvasnicka T; Dusková D; Poletínová S; Kieferová V
Cas Lek Cesk; 2012; 151(2):76-82. PubMed ID: 22515013
[TBL] [Abstract][Full Text] [Related]
28. Association of single nucleotide polymorphisms (4G/5G) of plasminogen activator inhibitor-1 and the risk factors for placenta-related obstetric complications.
Donmez HG; Beksac MS
Blood Coagul Fibrinolysis; 2023 Sep; 34(6):396-402. PubMed ID: 37577872
[TBL] [Abstract][Full Text] [Related]
29. Which thrombophilic gene mutations are risk factors for recurrent pregnancy loss?
Goodman CS; Coulam CB; Jeyendran RS; Acosta VA; Roussev R
Am J Reprod Immunol; 2006 Oct; 56(4):230-6. PubMed ID: 16938111
[TBL] [Abstract][Full Text] [Related]
30. Early pregnancy loss in celiac women: The role of genetic markers of thrombophilia.
Ciacci C; Tortora R; Scudiero O; Di Fiore R; Salvatore F; Castaldo G
Dig Liver Dis; 2009 Oct; 41(10):717-20. PubMed ID: 19395327
[TBL] [Abstract][Full Text] [Related]
31. The role of hypercoagulability in ischemic colitis.
Tsimperidis AG; Kapsoritakis AN; Linardou IA; Psychos AK; Papageorgiou AA; Vamvakopoulos NC; Kyriakou DS; Potamianos SP
Scand J Gastroenterol; 2015 Jul; 50(7):848-55. PubMed ID: 25656775
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. 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]
34. Interaction of heritable and estrogen-induced thrombophilia: possible etiologies for ischemic optic neuropathy and ischemic stroke.
Glueck CJ; Fontaine RN; Wang P
Thromb Haemost; 2001 Feb; 85(2):256-9. PubMed ID: 11246543
[TBL] [Abstract][Full Text] [Related]
35. The early-onset preeclampsia is associated with MTHFR and FVL polymorphisms.
Salimi S; Saravani M; Yaghmaei M; Fazlali Z; Mokhtari M; Naghavi A; Farajian-Mashhadi F
Arch Gynecol Obstet; 2015 Jun; 291(6):1303-12. PubMed ID: 25480409
[TBL] [Abstract][Full Text] [Related]
36. Correlation with Platelet Parameters and Genetic Markers of Thrombophilia Panel (Factor II g.20210G>A, Factor V Leiden, MTHFR (C677T, A1298C), PAI-1, β-Fibrinogen, Factor XIIIA (V34L), Glycoprotein IIIa (L33P)) in Ischemic Strokes.
Tasdemir S; Erdem HB; Sahin I; Ozel L; Ozdemir G; Eroz R; Tatar A
Neuromolecular Med; 2016 Jun; 18(2):170-6. PubMed ID: 26951304
[TBL] [Abstract][Full Text] [Related]
37. Prevalence of genetic markers for thrombophilia in recurrent pregnancy loss.
Carp H; Salomon O; Seidman D; Dardik R; Rosenberg N; Inbal A
Hum Reprod; 2002 Jun; 17(6):1633-7. PubMed ID: 12042290
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. 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]
40. 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]
[Previous] [Next] [New Search]
