119 related articles for article (PubMed ID: 17426795)
21. Metabolic characteristics of women who developed ovarian hyperstimulation syndrome.
Delvigne A; Kostyla K; De Leener A; Lejeune B; Cantiniaux B; Bergmann P; Rozenberg S
Hum Reprod; 2002 Aug; 17(8):1994-6. PubMed ID: 12151426
[TBL] [Abstract][Full Text] [Related]
22. The prevalence of methylenetetrahydrofolate reductase 677 C-T, factor V 1691 G-A, and prothrombin 20210 G-A mutations in healthy populations in Setif, Algeria.
Bourouba R; Houcher B; Djabi F; Egin Y; Akar N
Clin Appl Thromb Hemost; 2009 Oct; 15(5):529-34. PubMed ID: 18840629
[TBL] [Abstract][Full Text] [Related]
23. Prothrombin and factor V mutations in women with a history of thrombosis during pregnancy and the puerperium.
Gerhardt A; Scharf RE; Beckmann MW; Struve S; Bender HG; Pillny M; Sandmann W; Zotz RB
N Engl J Med; 2000 Feb; 342(6):374-80. PubMed ID: 10666427
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Impact of inherited thrombophilia on the risk of recurrent venous thromboembolism onset in Georgian population.
Pirtskhelani N; Kochiashvili N; Makhaldiani L; Pargalava N; Gaprindashvili E; Kartvelishvili K
Georgian Med News; 2014 Feb; (227):93-7. PubMed ID: 24632656
[TBL] [Abstract][Full Text] [Related]
26. [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; 44(5):18-26. PubMed ID: 16313049
[TBL] [Abstract][Full Text] [Related]
27. Evaluation of factor V Leiden, prothrombin and methylenetetrahydrofolate reductase gene mutations in patients with severe pregnancy complications in northern Finland.
Jarvenpaa J; Pakkila M; Savolainen ER; Perheentupa A; Jarvela I; Ryynanen M
Gynecol Obstet Invest; 2006; 62(1):28-32. PubMed ID: 16514238
[TBL] [Abstract][Full Text] [Related]
28. Transient focal neurological deficits during pregnancy in carriers of inherited thrombophilia.
Kupferminc MJ; Yair D; Bornstein NM; Lessing JB; Eldor A
Stroke; 2000 Apr; 31(4):892-5. PubMed ID: 10753994
[TBL] [Abstract][Full Text] [Related]
29. The association between inherited thrombophilias and pregnancy-related hypertension recurrence.
Mendilcioglu I; Bilgen T; Arikan Y; Keser I; Simsek M; Timuragaoglu A
Arch Gynecol Obstet; 2011 Oct; 284(4):837-41. PubMed ID: 21072525
[TBL] [Abstract][Full Text] [Related]
30. Screening for inherited thrombophilia might be warranted among Eastern Mediterranean sickle-beta-0 thalassemia patients.
Isma'eel H; Arnaout MS; Shamseddeen W; Mahfouz R; Zeineh N; Jradi O; Taher A
J Thromb Thrombolysis; 2006 Oct; 22(2):121-3. PubMed ID: 17008978
[TBL] [Abstract][Full Text] [Related]
31. 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
[TBL] [Abstract][Full Text] [Related]
32. Prevalence of genetic markers for thrombophilia in recurrent pregnancy loss.
Carp H; Salomon O; Seidman D; Dardik R; Rosenberg N; Inbal A
Hum Reprod; 2002 Jun; 17(6):1633-7. PubMed ID: 12042290
[TBL] [Abstract][Full Text] [Related]
33. Multiplex primer extension reaction and capillary electrophoresis to study the frequency of thrombophilia-related mutations in a spanish population.
Zafra-Ceres M; de Haro T; Gómez-Capilla JA; Farez-Vidal E; Poyatos A; Gómez-Llorente C
Clin Chim Acta; 2012 Aug; 413(15-16):1255-8. PubMed ID: 22521752
[TBL] [Abstract][Full Text] [Related]
34. 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
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. [Factor V Leiden, FII G20210A, MTHFR C677T mutations as risk factors for venous thrombosis during pregnancy and puerperium].
Dordević V; Rakićević L; Spasić M; Miković D; Kovać M; Radojković D
Vojnosanit Pregl; 2005 Mar; 62(3):201-5. PubMed ID: 15790048
[TBL] [Abstract][Full Text] [Related]
37. 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
[TBL] [Abstract][Full Text] [Related]
38. [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; 46(6):3-8. PubMed ID: 17974163
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Legg-perthes disease and heritable thrombophilia.
López-Franco M; González-Morán G; De Lucas JC; Llamas P; de Velasco JF; Vivancos JC; Epeldegui-Torre T
J Pediatr Orthop; 2005; 25(4):456-9. PubMed ID: 15958894
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
