189 related articles for article (PubMed ID: 22275392)
21. The prevalence of factor V (G1691A), MTHFR (C677T) and PT (G20210A) gene mutations in arterial thrombosis.
Ozmen F; Ozmen MM; Ozalp N; Akar N
Ulus Travma Acil Cerrahi Derg; 2009 Mar; 15(2):113-9. PubMed ID: 19353312
[TBL] [Abstract][Full Text] [Related]
22. Evaluation of the interactions of common genetic mutations in stroke subtypes.
Szolnoki Z; Somogyvári F; Kondacs A; Szabó M; Fodor L
J Neurol; 2002 Oct; 249(10):1391-7. PubMed ID: 12382154
[TBL] [Abstract][Full Text] [Related]
23. Stroke in children: inherited and acquired factors and age-related variations in the presentation of 48 paediatric patients.
Del Balzo F; Spalice A; Ruggieri M; Greco F; Properzi E; Iannetti P
Acta Paediatr; 2009 Jul; 98(7):1130-6. PubMed ID: 19432826
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. Case-control Study of methylenetetrahydrofolate reductase mutations and hyperhomocysteinemia and risk of stroke.
Almawi WY; Khan A; Al-Othman SS; Bakhiet M
J Stroke Cerebrovasc Dis; 2009; 18(5):407-8. PubMed ID: 19717029
[TBL] [Abstract][Full Text] [Related]
27. Posterior ocular involvement in Behçet's disease and thrombophilic mutations.
Vayá A; De la Fuente JM; Suescun M; España E; Ricart JM
Clin Hemorheol Microcirc; 2012; 51(3):225-8. PubMed ID: 22495315
[TBL] [Abstract][Full Text] [Related]
28. Genetic and acquired prothrombotic risk factors and sudden hearing loss.
Capaccio P; Ottaviani F; Cuccarini V; Bottero A; Schindler A; Cesana BM; Censuales S; Pignataro L
Laryngoscope; 2007 Mar; 117(3):547-51. PubMed ID: 17334320
[TBL] [Abstract][Full Text] [Related]
29. [Genetics of blood coagulation in young stroke patients].
Pongrácz E; Tordai A; Csornai M; Nagy Z
Ideggyogy Sz; 2002 Mar; 55(3-4):111-7. PubMed ID: 12122980
[TBL] [Abstract][Full Text] [Related]
30. Analysis of thrombophilic genetic mutations in patients with Sheehan's syndrome: is thrombophilia responsible for the pathogenesis of Sheehan's syndrome?
Gokalp D; Tuzcu A; Bahceci M; Ayyildiz O; Yurt M; Celik Y; Alpagat G
Pituitary; 2011 Jun; 14(2):168-73. PubMed ID: 21107737
[TBL] [Abstract][Full Text] [Related]
31. Factor V Leiden, prothrombin gene G20210A variant, and methylenetetrahydrofolate reductase C677T genotype in young adults with ischemic stroke.
Lopaciuk S; Bykowska K; Kwiecinski H; Mickielewicz A; Czlonkowska A; Mendel T; Kuczynska-Zardzewialy A; Szelagowska D; Windyga J; Schröder W; Herrmann FH; Jedrzejowska H
Clin Appl Thromb Hemost; 2001 Oct; 7(4):346-50. PubMed ID: 11697722
[TBL] [Abstract][Full Text] [Related]
32. Thrombophilia in young patients with acute myocardial infarction.
Celik M; Altintas A; Celik Y; Karabulut A; Ayyildiz O
Saudi Med J; 2008 Jan; 29(1):48-54. PubMed ID: 18176672
[TBL] [Abstract][Full Text] [Related]
33. Inherited prothrombotic risk factors in children with stroke, transient ischemic attack, or migraine.
Herak DC; Antolic MR; Krleza JL; Pavic M; Dodig S; Duranovic V; Brkic AB; Zadro R
Pediatrics; 2009 Apr; 123(4):e653-60. PubMed ID: 19336355
[TBL] [Abstract][Full Text] [Related]
34. Thrombophilic mutations as risk factor for retinal vein occlusion: a case-control study.
Russo PD; Damante G; Pasca S; Turello M; Barillari G
Clin Appl Thromb Hemost; 2015 May; 21(4):373-7. PubMed ID: 24569626
[TBL] [Abstract][Full Text] [Related]
35. MTHFR (C677T, A1298C), FV Leiden polymorphisms, and the prothrombin G20210A mutation in arterial ischemic stroke among young tunisian adults.
M'barek L; Sakka S; Meghdiche F; Turki D; Maalla K; Dammak M; Kallel C; Mhiri C
Metab Brain Dis; 2021 Mar; 36(3):421-428. PubMed ID: 33400068
[TBL] [Abstract][Full Text] [Related]
36. Thrombophilic polymorphisms - factor V Leiden G1691A, prothrombin G20210A and MTHFR C677T - in Tunisian patients with cerebral venous thrombosis.
Ben Salem-Berrabah O; Fekih-Mrissa N; N'siri B; Ben Hamida A; Benammar-Elgaaied A; Gritli N; Mrissa R
J Clin Neurosci; 2012 Sep; 19(9):1326-7. PubMed ID: 22721898
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Role of genetic and acquired prothrombotic risk factors in genesis of sudden sensorineural hearing loss.
Fusconi M; Chistolini A; Angelosanto N; Pignoloni P; Tombolini M; De Virgilio A; Pagliarella M; de Vincentiis M
Audiol Neurootol; 2011; 16(3):185-90. PubMed ID: 20798492
[TBL] [Abstract][Full Text] [Related]
39. The prevalence of factor V Leiden (G1691A), prothrombin G20210A and methylenetetrahydrofolate reductase C677T mutations in Jordanian patients with beta-thalassemia major.
Al-Sweedan SA; Jaradat S; Iraqi M; Beshtawi M
Blood Coagul Fibrinolysis; 2009 Dec; 20(8):675-8. PubMed ID: 19710606
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]