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Journal Abstract Search

524 related items for PubMed ID: 10835445

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  • 2. Sudden infant death syndrome, childhood thrombosis, and presence of genetic risk factors for thrombosis.
    Larsen TB, Nørgaard-Pedersen B, Lundemose JB, Rüdiger N, Gaustadnes M, Brandslund I.
    Thromb Res; 2000 May 15; 98(4):233-9. PubMed ID: 10822069
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  • 3. Factor V Leiden mutation and other thrombophilia markers in childhood ischemic stroke.
    Duran R, Biner B, Demir M, Celtik C, Karasalihoğlu S.
    Clin Appl Thromb Hemost; 2005 Jan 15; 11(1):83-8. PubMed ID: 15678277
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  • 4. 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 15; 40(1):65-70. PubMed ID: 18927445
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  • 5. 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 15; 66(1):28-31. PubMed ID: 11426488
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  • 8. A Study on Hereditary Thrombophilia and Stroke in a Cohort from Sri Lanka.
    Kalpage HA, Sumathipala DS, Goonasekara HW, Dissanayake VH.
    J Stroke Cerebrovasc Dis; 2016 Jan 15; 25(1):102-9. PubMed ID: 26522268
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  • 9. 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 15; 17(6):1633-7. PubMed ID: 12042290
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  • 10. 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 15; 35(5):629-35. PubMed ID: 12454577
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  • 11. 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 15; 7(4):346-50. PubMed ID: 11697722
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  • 13. Thrombophilia and immunological disorders in pregnancies as risk factors for small for gestational age infants.
    Verspyck E, Le Cam-Duchez V, Goffinet F, Tron F, Marpeau L, Borg JY.
    BJOG; 2002 Jan 15; 109(1):28-33. PubMed ID: 11843372
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  • 14. Thrombophilia as a multigenic disease.
    Zöller B, García de Frutos P, Hillarp A, Dahlbäck B.
    Haematologica; 1999 Jan 15; 84(1):59-70. PubMed ID: 10091393
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  • 15. 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 15; 6(2):104-7. PubMed ID: 10775032
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  • 18. 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 15; 19(3):189-96. PubMed ID: 16082606
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  • 19. Symptomatic ischemic stroke in full-term neonates : role of acquired and genetic prothrombotic risk factors.
    Günther G, Junker R, Sträter R, Schobess R, Kurnik K, Heller C, Kosch A, Nowak-Göttl U, Childhood Stroke Study Group.
    Stroke; 2000 Oct 15; 31(10):2437-41. PubMed ID: 11022077
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  • 20. 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 15; 83(2):229-33. PubMed ID: 10739378
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