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148 related items for PubMed ID: 10753994
21. Polycystic ovarian syndrome and thrombophilia. Tsanadis G, Vartholomatos G, Korkontzelos I, Avgoustatos F, Kakosimos G, Sotiriadis A, Tatsioni A, Eleftheriou A, Lolis D. Hum Reprod; 2002 Feb; 17(2):314-9. PubMed ID: 11821270 [Abstract] [Full Text] [Related]
22. Preconception counseling for women with thrombophilia. Silver RM, Warren JE. Clin Obstet Gynecol; 2006 Dec; 49(4):906-19. PubMed ID: 17082685 [Abstract] [Full Text] [Related]
23. Hereditary Thrombophilia and thrombotic events in pregnancy: single-center experience. Coriu L, Ungureanu R, Talmaci R, Uscatescu V, Cirstoiu M, Coriu D, Copaciu E. J Med Life; 2014 Dec; 7(4):567-71. PubMed ID: 25713624 [Abstract] [Full Text] [Related]
24. Maternal and fetal inherited thrombophilias are not related to the development of severe preeclampsia. Livingston JC, Barton JR, Park V, Haddad B, Phillips O, Sibai BM. Am J Obstet Gynecol; 2001 Jul; 185(1):153-7. PubMed ID: 11483920 [Abstract] [Full Text] [Related]
25. Factor V leiden and prothrombin G20210A mutations, but not methylenetetrahydrofolate reductase C677T, are associated with recurrent miscarriages. Foka ZJ, Lambropoulos AF, Saravelos H, Karas GB, Karavida A, Agorastos T, Zournatzi V, Makris PE, Bontis J, Kotsis A. Hum Reprod; 2000 Feb; 15(2):458-62. PubMed ID: 10655323 [Abstract] [Full Text] [Related]
26. 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]
27. Renal vascular sclerosis is associated with inherited thrombophilias. Goforth RL, Rennke H, Sethi S. Kidney Int; 2006 Aug; 70(4):743-50. PubMed ID: 16760910 [Abstract] [Full Text] [Related]
28. Absence of association of thrombophilia polymorphisms with intrauterine growth restriction. Infante-Rivard C, Rivard GE, Yotov WV, Génin E, Guiguet M, Weinberg C, Gauthier R, Feoli-Fonseca JC. N Engl J Med; 2002 Jul 04; 347(1):19-25. PubMed ID: 12097536 [Abstract] [Full Text] [Related]
29. Prevalence of three prothrombotic polymorphisms. Factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase (MTHFR) C 677T in Argentina. On behalf of the Grupo Cooperativo Argentino de Hemostasia y Trombosis. Genoud V, Castañon M, Annichino-Bizzacchi J, Korin J, Kordich L. Thromb Res; 2000 Nov 01; 100(3):127-31. PubMed ID: 11108898 [No Abstract] [Full Text] [Related]
30. Inherited risk factors for thrombophilia among children with Legg-Calvé-Perthes disease. Arruda VR, Belangero WD, Ozelo MC, Oliveira GB, Pagnano RG, Volpon JB, Annichino-Bizzacchi JM. J Pediatr Orthop; 1999 Nov 01; 19(1):84-7. PubMed ID: 9890294 [Abstract] [Full Text] [Related]
31. 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 01; 55(5):360-8. PubMed ID: 16635210 [Abstract] [Full Text] [Related]
32. [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 May 01; 44(5):18-26. PubMed ID: 16313049 [Abstract] [Full Text] [Related]
33. Risk of venous thrombosis in carriers of the prothrombin G20210A variant and factor V Leiden and their interaction with oral contraceptives. Aznar J, Vayá A, Estellés A, Mira Y, Seguí R, Villa P, Ferrando F, Falcó C, Corella D, España F. Haematologica; 2000 Dec 01; 85(12):1271-6. PubMed ID: 11114134 [Abstract] [Full Text] [Related]
34. Increased frequency of genetic thrombophilia in women with complications of pregnancy. Kupferminc MJ, Eldor A, Steinman N, Many A, Bar-Am A, Jaffa A, Fait G, Lessing JB. N Engl J Med; 1999 Jan 07; 340(1):9-13. PubMed ID: 9878639 [Abstract] [Full Text] [Related]
35. 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 07; 81(4):989-95. PubMed ID: 15066453 [Abstract] [Full Text] [Related]
36. Risk factors for clinical manifestations in carriers of Factor V Leiden and prothrombin gene mutations. DeSancho MT, Berlus N, Christos PJ, Rand J. Blood Coagul Fibrinolysis; 2010 Jan 07; 21(1):11-5. PubMed ID: 19474699 [Abstract] [Full Text] [Related]
37. Frequency of factor V, prothrombin and methylenetetrahydrofolate reductase gene variants in preeclampsia. D'Elia AV, Driul L, Giacomello R, Colaone R, Fabbro D, Di Leonardo C, Florio P, Petraglia F, Marchesoni D, Damante G. Gynecol Obstet Invest; 2002 Jan 07; 53(2):84-7. PubMed ID: 11961379 [Abstract] [Full Text] [Related]
38. The relationship between thrombophilic mutations and preeclampsia: a prospective case-control study. Yalinkaya A, Erdemoglu M, Akdeniz N, Kale A, Kale E. Ann Saudi Med; 2006 Jan 07; 26(2):105-9. PubMed ID: 16761446 [Abstract] [Full Text] [Related]
39. 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 07; 63(2):126-36. PubMed ID: 19906129 [Abstract] [Full Text] [Related]
40. The association of inherited thrombophilia and intrauterine fetal death: a case-control study. Helgadottir LB, Skjeldestad FE, Jacobsen AF, Sandset PM, Jacobsen EM. Blood Coagul Fibrinolysis; 2011 Dec 07; 22(8):651-6. PubMed ID: 22198364 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]