119 related articles for article (PubMed ID: 17426795)
1. Prevalence of inherited thrombophilia in patients with severe ovarian hyperstimulation syndrome.
Machac S; Lubusky M; Prochazka M; Streda R
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub; 2006 Nov; 150(2):289-92. PubMed ID: 17426795
[TBL] [Abstract][Full Text] [Related]
2. 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
[TBL] [Abstract][Full Text] [Related]
3. [Prevalence of thrombophilia in patients with severe ovarian hyperstimulation syndrome].
Machac S; Procházka M; Lubuský M
Ceska Gynekol; 2005 Jul; 70(4):254-7. PubMed ID: 16128122
[TBL] [Abstract][Full Text] [Related]
4. Increased prevalence of thrombophilia among women with severe ovarian hyperstimulation syndrome.
Dulitzky M; Cohen SB; Inbal A; Seidman DS; Soriano D; Lidor A; Mashiach S; Rabinovici J
Fertil Steril; 2002 Mar; 77(3):463-7. PubMed ID: 11872195
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. Thrombophilia and ovarian hyperstimulation syndrome: a case report.
Levy G; Lucidi RS
Hawaii Med J; 2011 May; 70(5):97-8. PubMed ID: 21857739
[TBL] [Abstract][Full Text] [Related]
9. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR G677A among 594 thrombotic Jordanian patients.
Eid SS; Shubeilat T
Blood Coagul Fibrinolysis; 2005 Sep; 16(6):417-21. PubMed ID: 16093732
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. [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]
13. 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]
14. Inherited thrombophilia polymorphisms and pregnancy outcomes in nulliparous women.
Said JM; Higgins JR; Moses EK; Walker SP; Borg AJ; Monagle PT; Brennecke SP
Obstet Gynecol; 2010 Jan; 115(1):5-13. PubMed ID: 20027027
[TBL] [Abstract][Full Text] [Related]
15. -455G/A beta-fibrinogen gene polymorphism, factor V Leiden, prothrombin G20210A mutation and MTHFR C677T, and placental vascular complications.
Camilleri RS; Peebles D; Portmann C; Everington T; Cohen H
Blood Coagul Fibrinolysis; 2004 Mar; 15(2):139-47. PubMed ID: 15091001
[TBL] [Abstract][Full Text] [Related]
16. Factor V Leiden and antiphospholipid antibodies are significant risk factors for ischemic stroke in children.
Kenet G; Sadetzki S; Murad H; Martinowitz U; Rosenberg N; Gitel S; Rechavi G; Inbal A
Stroke; 2000 Jun; 31(6):1283-8. PubMed ID: 10835445
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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
[TBL] [Abstract][Full Text] [Related]
19. Impact of thrombophilic genes mutations on thrombosis risk in Egyptian nonmetastatic cancer patients.
Wahba MA; Ismail MA; Saad AA; Habashy DM; Hafeez ZM; Boshnak NH
Blood Coagul Fibrinolysis; 2015 Apr; 26(3):309-15. PubMed ID: 25565385
[TBL] [Abstract][Full Text] [Related]
20. Prevalence of genetic mutations that predispose to thrombophilia in a Greek Cypriot population.
Angelopoulou K; Nicolaides A; Constantinou Deltas C
Clin Appl Thromb Hemost; 2000 Apr; 6(2):104-7. PubMed ID: 10775032
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
