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Results: 1 to 20 of 102

1.

Thrombophilic gene mutations in children with migraine.

Ferrara M, Capozzi L, Bertocco F, Ferrara D, Russo R.

Hematology. 2012 Mar;17(2):115-7. doi: 10.1179/102453312X13221316478010.

PMID:
22664050
[PubMed - indexed for MEDLINE]
2.

Thrombophilia and varicella zoster in children.

Ferrara M, Bertocco F, Ferrara D, Capozzi L.

Hematology. 2013 Mar;18(2):119-22. doi: 10.1179/1607845412Y.0000000055. Epub 2013 Jan 3.

PMID:
23321260
[PubMed - indexed for MEDLINE]
3.

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.

PMID:
10835445
[PubMed - indexed for MEDLINE]
Free Article
4.

Heritable thrombophilia and hypofibrinolysis. Possible causes of retinal vein occlusion.

Glueck CJ, Bell H, Vadlamani L, Gupta A, Fontaine RN, Wang P, Stroop D, Gruppo R.

Arch Ophthalmol. 1999 Jan;117(1):43-9.

PMID:
9930159
[PubMed - indexed for MEDLINE]
5.

Prevalence of thrombotic risk factors among beta-thalassemia patients from Western Iran.

Rahimi Z, Ghaderi M, Nagel RL, Muniz A.

J Thromb Thrombolysis. 2008 Dec;26(3):229-33. Epub 2007 Nov 4.

PMID:
17982733
[PubMed - indexed for MEDLINE]
6.

Lack of association between inherited thrombophilic risk factors and idiopathic sudden sensorineural hearing loss in Italian patients.

Cadoni G, Scipione S, Rocca B, Agostino S, La Greca C, Bonvissuto D, Paludetti G.

Ann Otol Rhinol Laryngol. 2006 Mar;115(3):195-200.

PMID:
16572609
[PubMed - indexed for MEDLINE]
7.

Impact of thrombophilic genetic factors on pulmonary embolism: early onset and recurrent incidences.

Ivanov P, Komsa-Penkova R, Kovacheva K, Ivanov Y, Stoyanova A, Ivanov I, Pavlov P, Glogovska P, Nojarov V.

Lung. 2008 Jan-Feb;186(1):27-36. Epub 2007 Dec 21.

PMID:
18097719
[PubMed - indexed for MEDLINE]
8.

Prevalence of factor V G1691A (Leiden), prothrombin G20210A, and methylene tetrahydrofolate reductase C677T thrombophilic mutations in children with inflammatory bowel disease.

Kader HA, Berman WF, Al-Seraihy AS, Ware RE, Ulshen MH, Treem WR.

J Pediatr Gastroenterol Nutr. 2002 Nov;35(5):629-35.

PMID:
12454577
[PubMed - indexed for MEDLINE]
9.

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
[PubMed - indexed for MEDLINE]
10.

Factor V Leiden and prothrombin gene mutation may predispose to paradoxical embolism in subjects with patent foramen ovale.

Karttunen V, Hiltunen L, Rasi V, Vahtera E, Hillbom M.

Blood Coagul Fibrinolysis. 2003 Apr;14(3):261-8.

PMID:
12695749
[PubMed - indexed for MEDLINE]
11.

Primary thrombophilia in Mexico. II. Factor V G1691A (Leiden), prothrombin G20210A, and methylenetetrahydrofolate reductase C677T polymorphism in thrombophilic Mexican mestizos.

Ruiz-Argüelles GJ, Garcés-Eisele J, Reyes-Núñez V, Ramírez-Cisneros FJ.

Am J Hematol. 2001 Jan;66(1):28-31.

PMID:
11426488
[PubMed - indexed for MEDLINE]
12.

Contribution of prothrombin 20210A allele and factor V Leiden mutation to thrombosis risk in thrombophilic families with other hemostatic deficiencies.

Tirado I, Mateo J, Soria JM, Oliver A, Borrell M, Coll I, Vallvé C, Souto JC, Martínez-Sánchez E, Fontcuberta J.

Haematologica. 2001 Nov;86(11):1200-8.

PMID:
11694407
[PubMed - indexed for MEDLINE]
Free Article
13.

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 10;342(6):374-80.

PMID:
10666427
[PubMed - indexed for MEDLINE]
Free Article
14.

Prediction of ischemic stroke in young Indians: is thrombophilia profiling a way out?

Chatterjee T, Gupta N, Choudhry VP, Behari M, Saxena R, Ashraf MZ.

Blood Coagul Fibrinolysis. 2013 Jun;24(4):449-53. doi: 10.1097/MBC.0b013e32835bfe21.

PMID:
23337710
[PubMed - indexed for MEDLINE]
15.

Thrombophilic polymorphisms--factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations--and preterm birth.

Resch B, Gallistl S, Kutschera J, Mannhalter C, Muntean W, Mueller WD.

Wien Klin Wochenschr. 2004 Sep 30;116(17-18):622-6.

PMID:
15515881
[PubMed - indexed for MEDLINE]
16.

Factor v Leiden and antiphospholipid antibodies in either mothers or infants increase the risk for perinatal arterial ischemic stroke.

Simchen MJ, Goldstein G, Lubetsky A, Strauss T, Schiff E, Kenet G.

Stroke. 2009 Jan;40(1):65-70. doi: 10.1161/STROKEAHA.108.527283. Epub 2008 Oct 16.

PMID:
18927445
[PubMed - indexed for MEDLINE]
Free Article
17.

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
[PubMed - indexed for MEDLINE]
18.

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
[PubMed - indexed for MEDLINE]
19.

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;55(5):360-8.

PMID:
16635210
[PubMed - indexed for MEDLINE]
20.

[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. Bulgarian.

PMID:
18333414
[PubMed - indexed for MEDLINE]

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