174 related articles for article (PubMed ID: 38674167)
1. 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]
2. 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]
3. Variant alleles in factor V, prothrombin, plasminogen activator inhibitor-1, methylenetetrahydrofolate reductase and risk of thromboembolism in metastatic colorectal cancer patients treated with first-line chemotherapy plus bevacizumab.
Falvella FS; Cremolini C; Miceli R; Nichetti F; Cheli S; Antoniotti C; Infante G; Martinetti A; Marmorino F; Sottotetti E; Berenato R; Caporale M; Colombo A; de Braud F; Di Bartolomeo M; Clementi E; Loupakis F; Pietrantonio F
Pharmacogenomics J; 2017 Jul; 17(4):331-336. PubMed ID: 27001121
[TBL] [Abstract][Full Text] [Related]
4. Analysis of thrombophilic genetic mutations in patients with Sheehan's syndrome: is thrombophilia responsible for the pathogenesis of Sheehan's syndrome?
Gokalp D; Tuzcu A; Bahceci M; Ayyildiz O; Yurt M; Celik Y; Alpagat G
Pituitary; 2011 Jun; 14(2):168-73. PubMed ID: 21107737
[TBL] [Abstract][Full Text] [Related]
5. Plasminogen activator inhibitor-1, factor V, factor II and methylenetetrahydrofolate reductase polymorphisms in women with recurrent miscarriage.
Pietropolli A; Giuliani E; Bruno V; Patrizi L; Piccione E; Ticconi C
J Obstet Gynaecol; 2014 Apr; 34(3):229-34. PubMed ID: 24484533
[TBL] [Abstract][Full Text] [Related]
6. Prothrombin polymorphism A19911G, factor V HR2 haplotype A4070G, and plasminogen activator-inhibitor-1 polymorphism 4G/5G and the risk of retinal vein occlusion.
Kuhli-Hattenbach C; Hellstern P; Nägler DK; Kohnen T; Hattenbach LO
Ophthalmic Genet; 2017; 38(5):413-417. PubMed ID: 28085526
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Prevalence of factor V G1691A (Leiden), prothrombin G20210A, and methylene tetrahydrofolate reductase C677T thrombophilic mutations in children with inflammatory bowel disease.
Kader HA; Berman WF; Al-Seraihy AS; Ware RE; Ulshen MH; Treem WR
J Pediatr Gastroenterol Nutr; 2002 Nov; 35(5):629-35. PubMed ID: 12454577
[TBL] [Abstract][Full Text] [Related]
9. Interaction of thrombophilic SNPs in patients with unexplained infertility-multifactor dimensionality reduction (MDR) model analysis.
Milenkovic J; Milojkovic M; Mitic D; Stoimenov TJ; Smelcerovic Z; Stojanovic D; Vujic S; Bojanic N
J Assist Reprod Genet; 2020 Jun; 37(6):1449-1458. PubMed ID: 32399796
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Multiple thrombophilic gene mutations rather than specific gene mutations are risk factors for recurrent miscarriage.
Coulam CB; Jeyendran RS; Fishel LA; Roussev R
Am J Reprod Immunol; 2006 May; 55(5):360-8. PubMed ID: 16635210
[TBL] [Abstract][Full Text] [Related]
12. Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations.
Ozdemir O; Yenicesu GI; Silan F; Köksal B; Atik S; Ozen F; Göl M; Cetin A
Genet Test Mol Biomarkers; 2012 Apr; 16(4):279-86. PubMed ID: 22047507
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. A prospective case-control study analyzes 12 thrombophilic gene mutations in Turkish couples with recurrent pregnancy loss.
Yenicesu GI; Cetin M; Ozdemir O; Cetin A; Ozen F; Yenicesu C; Yildiz C; Kocak N
Am J Reprod Immunol; 2010 Feb; 63(2):126-36. PubMed ID: 19906129
[TBL] [Abstract][Full Text] [Related]
15. The effects of genetic polymorphisms and diabetes mellitus on the development of peripheral artery disease.
Yalım Z; Tutgun Onrat S; Alan S; Aldemir M; Avşar A; Doğan İ; Onrat E
Turk Kardiyol Dern Ars; 2020 Jul; 48(5):484-493. PubMed ID: 32633259
[TBL] [Abstract][Full Text] [Related]
16. Comparison of thrombophilic gene mutations among patients experiencing recurrent miscarriage and deep vein thrombosis.
Coulam CB; Wallis D; Weinstein J; DasGupta DS; Jeyendran RS
Am J Reprod Immunol; 2008 Nov; 60(5):426-31. PubMed ID: 18803625
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. [Genetic thrombophilic defects (Factor V Leiden, prothrombin G20210A, MTHFR C677T) in women with recurrent fetal loss].
Kovacheva K; Ivanov P; Konova E; Simeonova M; Komsa-Penkova R
Akush Ginekol (Sofiia); 2007; 46(7):10-6. PubMed ID: 18333414
[TBL] [Abstract][Full Text] [Related]
19. The factor V Leiden mutation, high factor VIII, and high plasminogen activator inhibitor activity: etiologies for sporadic miscarriage.
Glueck CJ; Pranikoff J; Aregawi D; Haque M; Zhu B; Tracy T; Wang P
Metabolism; 2005 Oct; 54(10):1345-9. PubMed ID: 16154434
[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]
