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339 related items for PubMed ID: 18957855
1. Repeated in vitro fertilization failure and its relation with thrombophilia. Simur A, Ozdemir S, Acar H, Colakoğlu MC, Görkemli H, Balci O, Nergis S. Gynecol Obstet Invest; 2009; 67(2):109-12. PubMed ID: 18957855 [Abstract] [Full Text] [Related]
2. Acquired and inherited thrombophilia: implication in recurrent IVF and embryo transfer failure. Qublan HS, Eid SS, Ababneh HA, Amarin ZO, Smadi AZ, Al-Khafaji FF, Khader YS. Hum Reprod; 2006 Oct; 21(10):2694-8. PubMed ID: 16835215 [Abstract] [Full Text] [Related]
3. Embryo implantation after assisted reproductive procedures and maternal thrombophilia. Martinelli I, Taioli E, Ragni G, Levi-Setti P, Passamonti SM, Battaglioli T, Lodigiani C, Mannucci PM. Haematologica; 2003 Jul; 88(7):789-93. PubMed ID: 12857558 [Abstract] [Full Text] [Related]
4. [Risk of thrombophilia in carriers of thrombophilic genetic factors in unsuccessful assisted reproduction]. Ivanov P, Komsa-Penkova R, Kovacheva K, Konova E, Todorova K, Simeonova M, Ivanov I, Stoĭkov S, Popov I, Tanchev S, Bozhinova S. Akush Ginekol (Sofiia); 2007 Jul; 46(6):3-8. PubMed ID: 17974163 [Abstract] [Full Text] [Related]
5. Prevalence of thrombophilia in women with severe ovarian hyperstimulation syndrome and cost-effectiveness of screening. Fábregues F, Tàssies D, Reverter JC, Carmona F, Ordinas A, Balasch J. Fertil Steril; 2004 Apr; 81(4):989-95. PubMed ID: 15066453 [Abstract] [Full Text] [Related]
6. [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 Apr; 46(7):10-6. PubMed ID: 18333414 [Abstract] [Full Text] [Related]
7. Factor V Leiden and prothrombin gene G20210A mutation and in vitro fertilization: prospective cohort study. Ricci G, Bogatti P, Fischer-Tamaro L, Giolo E, Luppi S, Montico M, Ronfani L, Morgutti M. Hum Reprod; 2011 Nov; 26(11):3068-77. PubMed ID: 21868400 [Abstract] [Full Text] [Related]
9. 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 [Abstract] [Full Text] [Related]
10. Inherited thrombophilia: a possible cause of in utero vascular thrombosis in children with intestinal atresia. Johnson SM, Meyers RL. J Pediatr Surg; 2001 Aug; 36(8):1146-9. PubMed ID: 11479844 [Abstract] [Full Text] [Related]
11. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians. Eid SS, Rihani G. Clin Lab Sci; 2004 Aug; 17(4):200-2. PubMed ID: 15559724 [Abstract] [Full Text] [Related]
12. [Genomic diagnosis of thrombophilia in women: clinical relevance]. Luxembourg B, Lindhoff-Last E. Hamostaseologie; 2007 Feb; 27(1):22-31. PubMed ID: 17279273 [Abstract] [Full Text] [Related]
13. Low-molecular-weight heparin in the treatment of recurrent IVF-ET failure and thrombophilia: a prospective randomized placebo-controlled trial. Qublan H, Amarin Z, Dabbas M, Farraj AE, Beni-Merei Z, Al-Akash H, Bdoor AN, Nawasreh M, Malkawi S, Diab F, Al-Ahmad N, Balawneh M, Abu-Salim A. Hum Fertil (Camb); 2008 Dec; 11(4):246-53. PubMed ID: 19085261 [Abstract] [Full Text] [Related]
14. 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 [Abstract] [Full Text] [Related]
15. The prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian antenatal population. Said JM, Brennecke SP, Moses EK, Walker SP, Monagle PT, Campbell J, Bryant VJ, Borg AJ, Higgins JR. Aust N Z J Obstet Gynaecol; 2008 Dec; 48(6):536-41. PubMed ID: 19133039 [Abstract] [Full Text] [Related]
16. 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 [Abstract] [Full Text] [Related]
17. 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 [Abstract] [Full Text] [Related]
18. Multiple thrombophilic single nucleotide polymorphisms lack a significant effect on outcomes in fresh IVF cycles: an analysis of 1717 patients. Patounakis G, Bergh E, Forman EJ, Tao X, Lonczak A, Franasiak JM, Treff N, Scott RT. J Assist Reprod Genet; 2016 Jan; 33(1):67-73. PubMed ID: 26545911 [Abstract] [Full Text] [Related]
19. [IVF failures: maternal thrombophilia as a possible cause]. Dzhandzhgava ZhG, Bitsadze VO. Georgian Med News; 2005 Jan; (124-125):23-6. PubMed ID: 16148370 [Abstract] [Full Text] [Related]
20. Frequency of selected thrombophilias in women with placental abruption. Procházka M, Lubuský M, Slavík L, Hrachovec P, Zielina P, Kudela M, Lindqvist PG. Aust N Z J Obstet Gynaecol; 2007 Aug; 47(4):297-301. PubMed ID: 17627684 [Abstract] [Full Text] [Related] Page: [Next] [New Search]