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Journal Abstract Search

128 related items for PubMed ID: 10823289

  • 21.
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  • 22. Deep vein thrombosis followed by internal jugular vein thrombosis as a complication of in vitro fertilization in a woman heterozygous for the prothrombin 3' UTR and factor V Leiden mutations.
    McGowan BM, Kay LA, Perry DJ.
    Am J Hematol; 2003 Aug; 73(4):276-8. PubMed ID: 12879433
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  • 23. Factor V Leiden (G1691A) and prothrombin gene G20210A mutations as potential risk factors for venous thromboembolism after total hip or total knee replacement surgery.
    Wåhlander K, Larson G, Lindahl TL, Andersson C, Frison L, Gustafsson D, Bylock A, Eriksson BI.
    Thromb Haemost; 2002 Apr; 87(4):580-5. PubMed ID: 12008938
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  • 24. [Phenprocoumon-associated necrotizing hepatitis].
    Weber T, Hinterreiter M, Knoflach P.
    Dtsch Med Wochenschr; 2001 Sep 21; 126(38):1060. PubMed ID: 11565062
    [No Abstract] [Full Text] [Related]

  • 25. [Resistance to warfarin in a patient with hereditary thrombophilia].
    Haastrup P, Rudbæk T, Bove J.
    Ugeskr Laeger; 2013 Oct 21; 175(43):2572-3. PubMed ID: 24629157
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  • 28. Venous thromboembolism in a young woman with combined homozygosity for factor V Leiden and prothrombin G20210A mutations.
    Leonard M, Gala JL, Verschuren F, Coche E, Deneys V, Hainaut P.
    Haematologica; 2005 Nov 21; 90 Suppl():ECR30. PubMed ID: 16266921
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  • 29. [Portal-splenic-mesenteric venous thrombosis secondary to a mutation of the prothrombin gene].
    Frutos Bernal MD, Fernández Hernández JA, Carrasco Prats M, Soria Cogollos T, Luján Mompeán JA, Hernández Agüera Q, Parrilla Paricio P.
    Gastroenterol Hepatol; 2005 Nov 21; 28(6):329-32. PubMed ID: 15989814
    [Abstract] [Full Text] [Related]

  • 30. Renal failure due to renal vein thrombosis in a fetus with growth restriction and thrombophilia.
    Has R, Corbacioglu Esmer A, Kalelioglu IH, Yumru H, Yüksel A, Ziylan O.
    J Obstet Gynaecol Res; 2014 Apr 21; 40(4):1124-7. PubMed ID: 24612313
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  • 31.
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  • 32.
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  • 33.
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  • 34. Phenprocoumon-induced liver disease ranges from mild acute hepatitis to (sub-) acute liver failure.
    Schimanski CC, Burg J, Möhler M, Höhler T, Kanzler S, Otto G, Galle PR, Lohse AW.
    J Hepatol; 2004 Jul 21; 41(1):67-74. PubMed ID: 15246210
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  • 35.
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  • 36. Thrombophilia: a genetic predisposition to thrombosis.
    Sacher RA.
    Trans Am Clin Climatol Assoc; 1999 Jul 21; 110():51-60; discussion 60-1. PubMed ID: 10344006
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  • 37. Primary upper-extremity deep vein thrombosis: high prevalence of thrombophilic defects.
    Hendler MF, Meschengieser SS, Blanco AN, Alberto MF, Salviú MJ, Gennari L, Lazzari MA.
    Am J Hematol; 2004 Aug 21; 76(4):330-7. PubMed ID: 15282664
    [Abstract] [Full Text] [Related]

  • 38. Inherited and acquired thrombophilic alterations in patients with superficial vein thrombosis of lower limbs.
    Legnani C, Cini M, Cosmi B, Filippini M, Favaretto E, Palareti G.
    Thromb Haemost; 2014 Jun 21; 111(6):1194-6. PubMed ID: 24500135
    [No Abstract] [Full Text] [Related]

  • 39. [Off-label use in long-term anticoagulation after liver transplantation due to phenprocoumon-induced hepatic failure].
    Bertsche T, Fritz R, Sauer P, Encke J, Haefeli WE, Walter-Sack I.
    Med Klin (Munich); 2005 Dec 15; 100(12):820-4. PubMed ID: 16453097
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  • 40.
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