365 related articles for article (PubMed ID: 16450127)
1. Thrombophilic mutations in Iranian patients with infertility and recurrent spontaneous abortion.
Behjati R; Modarressi MH; Jeddi-Tehrani M; Dokoohaki P; Ghasemi J; Zarnani AH; Aarabi M; Memariani T; Ghaffari M; Akhondi MA
Ann Hematol; 2006 Apr; 85(4):268-71. PubMed ID: 16450127
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. 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]
4. [Relationship between three thrombophilic gene mutations and unexplained recurrent early spontaneous abortion].
Xu L; Liu XM; Zhang HY; Zhao J; Qi QW; Chang YF
Zhonghua Fu Chan Ke Za Zhi; 2007 Mar; 42(3):180-3. PubMed ID: 17537304
[TBL] [Abstract][Full Text] [Related]
5. MTHFR C677T Polymorphism and factor V Leiden mutation are not associated with recurrent spontaneous abortion of unexplained etiology in Japanese women.
Kobashi G; Kato EH; Morikawa M; Shimada S; Ohta K; Fujimoto S; Minakami H; Yamada H
Semin Thromb Hemost; 2005 Jun; 31(3):266-71. PubMed ID: 16052395
[TBL] [Abstract][Full Text] [Related]
6. Combined thrombophilic mutations in women with unexplained recurrent miscarriage.
Sotiriadis A; Vartholomatos G; Pavlou M; Kolaitis N; Dova L; Stefos T; Paraskevaidis E; Kalantaridou SN
Am J Reprod Immunol; 2007 Feb; 57(2):133-41. PubMed ID: 17217367
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. Genetic thrombophilic mutations among couples with recurrent miscarriage.
Jivraj S; Rai R; Underwood J; Regan L
Hum Reprod; 2006 May; 21(5):1161-5. PubMed ID: 16431900
[TBL] [Abstract][Full Text] [Related]
11. Thrombophilia-related genetic variations in patients with pulmonary embolism in the main teaching hospital in Jordan.
Obeidat NM; Awidi A; Sulaiman NA; Abu-Khader IB
Saudi Med J; 2009 Jul; 30(7):921-5. PubMed ID: 19618008
[TBL] [Abstract][Full Text] [Related]
12. Molecular analysis of factor V Leiden, factor V Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients.
Dölek B; Eraslan S; Eroğlu S; Kesim BE; Ulutin T; Yalçiner A; Laleli YR; Gözükirmizi N
Clin Appl Thromb Hemost; 2007 Oct; 13(4):435-8. PubMed ID: 17911197
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Inherited thrombophilia in infertile women: implication in unexplained infertility.
Casadei L; Puca F; Privitera L; Zamaro V; Emidi E
Fertil Steril; 2010 Jul; 94(2):755-7. PubMed ID: 19939360
[TBL] [Abstract][Full Text] [Related]
15. Cerebral venous and sinus thrombosis and thrombophilic mutations in Western Iran: association with factor V Leiden.
Rahimi Z; Mozafari H; Bigvand AH; Doulabi RM; Vaisi-Raygani A; Afshari D; Razazian N; Rezaei M
Clin Appl Thromb Hemost; 2010 Aug; 16(4):430-4. PubMed ID: 19703820
[TBL] [Abstract][Full Text] [Related]
16. Thrombophilic genes alterations as risk factor for recurrent pregnancy loss.
Farahmand K; Totonchi M; Hashemi M; Reyhani Sabet F; Kalantari H; Gourabi H; Mohseni Meybodi A
J Matern Fetal Neonatal Med; 2016; 29(8):1269-73. PubMed ID: 26135458
[TBL] [Abstract][Full Text] [Related]
17. Paternal thrombophilic gene mutations are not associated with recurrent miscarriage.
Toth B; Vocke F; Rogenhofer N; Friese K; Thaler CJ; Lohse P
Am J Reprod Immunol; 2008 Oct; 60(4):325-32. PubMed ID: 18754836
[TBL] [Abstract][Full Text] [Related]
18. Factor V Leiden G1691A and factor II G20210A point mutations and pregnancy in North-West of Iran.
Bagheri M; Rad IA; Nanbakhsh F
Arch Gynecol Obstet; 2011 Nov; 284(5):1311-5. PubMed ID: 21773779
[TBL] [Abstract][Full Text] [Related]
19. [C677T and A1298C mutation of the methylenetetrahydrofolate reductase gene in unexplained recurrent spontaneous abortion].
Wang XP; Lin QD; Ma ZW; Zhao AM
Zhonghua Fu Chan Ke Za Zhi; 2004 Apr; 39(4):238-41. PubMed ID: 15130349
[TBL] [Abstract][Full Text] [Related]
20. [Prothrombotic gene mutations in women with recurrent abortions and intrauterine fetal death].
Santoro R; Iannaccaro P; Sottilotta G
Minerva Ginecol; 2005 Aug; 57(4):447-50. PubMed ID: 16170289
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]