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Items: 1 to 20 of 160

1.

Prothrombotic genetic risk factors in stroke: a possible different role in pediatric and adult patients.

Djordjevic V, Stankovic M, Brankovic-Sreckovic V, Rakicevic L, Damnjanovic T, Antonijevic N, Radojkovic D.

Clin Appl Thromb Hemost. 2012 Nov;18(6):658-61. doi: 10.1177/1076029611432136. Epub 2012 Jan 23.

PMID:
22275392
2.

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.

PMID:
11697722
3.

The role of classic risk factors and prothrombotic factor gene mutations in ischemic stroke risk development in young and middle-aged individuals.

Supanc V, Sonicki Z, Vukasovic I, Solter VV, Zavoreo I, Kes VB.

J Stroke Cerebrovasc Dis. 2014 Mar;23(3):e171-6. doi: 10.1016/j.jstrokecerebrovasdis.2013.09.025. Epub 2013 Nov 1.

PMID:
24189452
4.
5.

Inherited thrombophilia as a risk factor for the development of ischemic stroke in young adults.

Voetsch B, Damasceno BP, Camargo EC, Massaro A, Bacheschi LA, Scaff M, Annichino-Bizzacchi JM, Arruda VR.

Thromb Haemost. 2000 Feb;83(2):229-33.

PMID:
10739378
6.

Genetic risk factors for arterial ischemic stroke in children: a possible MTHFR and eNOS gene-gene interplay?

Djordjevic V, Stankovic M, Brankovic-Sreckovic V, Rakicevic L, Radojkovic D.

J Child Neurol. 2009 Jul;24(7):823-7. doi: 10.1177/0883073808330164. Epub 2009 Apr 15.

PMID:
19372095
7.
8.

Inherited thrombophilia in childhood arterial stroke: data from Lebanon.

Muwakkit SA, Majdalani M, Hourani R, Mahfouz RA, Otrock ZK, Bilalian C, Chan AK, Abboud M, Mikati MA.

Pediatr Neurol. 2011 Sep;45(3):155-8. doi: 10.1016/j.pediatrneurol.2011.03.002.

PMID:
21824561
9.

Prothrombotic conditions, oral contraceptives, and the risk of ischemic stroke.

Slooter AJ, Rosendaal FR, Tanis BC, Kemmeren JM, van der Graaf Y, Algra A.

J Thromb Haemost. 2005 Jun;3(6):1213-7.

10.

Factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations are not associated with chronic limb ischemia: the Linz Peripheral Arterial Disease (LIPAD) study.

Mueller T, Marschon R, Dieplinger B, Haidinger D, Gegenhuber A, Poelz W, Webersinke G, Haltmayer M.

J Vasc Surg. 2005 May;41(5):808-15.

11.

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. doi: 10.1097/MBC.0b013e3283255487.

PMID:
19349859
12.

Lipoprotein (a) and genetic polymorphisms of clotting factor V, prothrombin, and methylenetetrahydrofolate reductase are risk factors of spontaneous ischemic stroke in childhood.

Nowak-Göttl U, Sträter R, Heinecke A, Junker R, Koch HG, Schuierer G, von Eckardstein A.

Blood. 1999 Dec 1;94(11):3678-82.

PMID:
10572079
13.

Role of thrombophilic risk factors in children with non-stroke cerebral palsy.

Fattal-Valevski A, Kenet G, Kupferminc MJ, Mesterman R, Leitner Y, Rimon E, Harel S, Hassner A.

Thromb Res. 2005;116(2):133-7. Epub 2004 Dec 29.

PMID:
15907528
14.

Prevalence of thrombophilic mutations and ACE I/D polymorphism in Turkish ischemic stroke patients.

Celiker G, Can U, Verdi H, Yazici AC, Ozbek N, Atac FB.

Clin Appl Thromb Hemost. 2009 Jul-Aug;15(4):415-20. doi: 10.1177/1076029608315163. Epub 2008 Apr 2.

PMID:
18387982
15.

Genetic background of nontraumatic osteonecrosis of the femoral head in the Korean population.

Chang JD, Hur M, Lee SS, Yoo JH, Lee KM.

Clin Orthop Relat Res. 2008 May;466(5):1041-6. doi: 10.1007/s11999-008-0147-1. Epub 2008 Mar 19.

16.

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. doi: 10.1007/s11102-010-0276-x.

PMID:
21107737
17.

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;63(2):126-36. doi: 10.1111/j.1600-0897.2009.00770.x. Epub 2009 Nov 10.

PMID:
19906129
19.

[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. Bulgarian.

PMID:
17974163
20.

Factor V Leiden G1691A, prothrombin G20210A, and MTHFR C677T mutations in Turkish inflammatory bowel disease patients.

Yasa MH, Bolaman Z, Yukselen V, Kadikoylu G, Karaoglul AO, Batun S.

Hepatogastroenterology. 2007 Jul-Aug;54(77):1438-42.

PMID:
17708272

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