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Journal Abstract Search

175 related items for PubMed ID: 10599098

  • 21. The risk of first venous thromboembolism during pregnancy and puerperium in double heterozygotes for factor V Leiden and prothrombin G20210A.
    Martinelli I, Battaglioli T, De Stefano V, Tormene D, Valdrè L, Grandone E, Tosetto A, Mannucci PM, GIT (Gruppo Italiano Trombofilia).
    J Thromb Haemost; 2008 Mar; 6(3):494-8. PubMed ID: 18182035
    [Abstract] [Full Text] [Related]

  • 22. A case of purpura fulminans secondary to transient protein C deficiency as a complication of chickenpox infection.
    Canpolat C, Bakir M.
    Turk J Pediatr; 2002 Mar; 44(2):148-51. PubMed ID: 12026205
    [Abstract] [Full Text] [Related]

  • 23. Risk factors and recurrence rate of primary deep vein thrombosis of the upper extremities.
    Martinelli I, Battaglioli T, Bucciarelli P, Passamonti SM, Mannucci PM.
    Circulation; 2004 Aug 03; 110(5):566-70. PubMed ID: 15262837
    [Abstract] [Full Text] [Related]

  • 24. Severe autoimmune protein S deficiency in a boy with idiopathic purpura fulminans.
    Bergmann F, Hoyer PF, D'Angelo SV, Mazzola G, Oestereich C, Barthels M, D'Angelo A.
    Br J Haematol; 1995 Mar 03; 89(3):610-4. PubMed ID: 7734361
    [Abstract] [Full Text] [Related]

  • 25. Purpura fulminans in a child as a complication of chickenpox infection.
    Campanelli A, Kaya G, Ozsahin AH, La Scala G, Jacquier C, Stauffer M, Boehlen F, de Moerloose P, Saurat JH.
    Dermatology; 2004 Mar 03; 208(3):262-4. PubMed ID: 15118384
    [Abstract] [Full Text] [Related]

  • 26. Basilar artery thrombosis in a child heterozygous for prothrombin gene G20210A mutation.
    Hüdaoglu O, Kurul S, Yis U, Dirik E, Cakmakçi H, Men S.
    J Child Neurol; 2007 Mar 03; 22(3):329-31. PubMed ID: 17621506
    [Abstract] [Full Text] [Related]

  • 27. AB0 blood group and risk of venous or arterial thrombosis in carriers of factor V Leiden or prothrombin G20210A polymorphisms.
    Miñano A, Ordóñez A, España F, González-Porras JR, Lecumberri R, Fontcuberta J, Llamas P, Marín F, Estellés A, Alberca I, Vicente V, Corral J.
    Haematologica; 2008 May 03; 93(5):729-34. PubMed ID: 18387978
    [Abstract] [Full Text] [Related]

  • 28. Concomitant heterozygous factor V Leiden mutation and homozygous prothrombin gene variant (G20210A) in patient with cerebral venous thrombosis.
    Kurkowska-Jastrzebska I, Wicha W, Dowzenko A, Vertun-Baranowska B, Pytlewski A, Bogusławska R, Członkowska A.
    Med Sci Monit; 2003 May 03; 9(5):CS41-5. PubMed ID: 12761462
    [Abstract] [Full Text] [Related]

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  • 30. Spontaneous superficial vein thrombosis in a young patient double heterozygous for factor V Leiden and the prothrombin G20210A mutation: a case report.
    Vayá A, Llopis I, Trenor R, Mira Y, Estellés A, Aznar J.
    Haematologica; 2000 May 03; 85(E-letters):E11. PubMed ID: 11114826
    [No Abstract] [Full Text] [Related]

  • 31. [Post-chickenpox purpura fulminans with transient reduction of C and S proteins].
    Angeles Fernández G, Villanueva Lamas J, Cambra FJ, Toll MT, Palomeque Rico A.
    An Esp Pediatr; 1998 Oct 03; 49(4):412-4. PubMed ID: 9859560
    [No Abstract] [Full Text] [Related]

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  • 33. Prevalence of factor V G1691A (factor V-Leiden) and prothrombin G20210A gene mutations in a recurrent miscarriage population.
    Finan RR, Tamim H, Ameen G, Sharida HE, Rashid M, Almawi WY.
    Am J Hematol; 2002 Dec 03; 71(4):300-5. PubMed ID: 12447960
    [Abstract] [Full Text] [Related]

  • 34. Ulcerative colitis presenting as purpura fulminans.
    Kempton CL, Bagby G, Collins JF.
    Inflamm Bowel Dis; 2001 Nov 03; 7(4):319-22. PubMed ID: 11720322
    [Abstract] [Full Text] [Related]

  • 35. The G20210A prothrombin polymorphism is not associated with increased thromboembolic risk in a large protein C deficient kindred.
    Bovill EG, Hasstedt SJ, Callas PW, Valliere JE, Scott BT, Bauer KA, Long GL.
    Thromb Haemost; 2000 Mar 03; 83(3):366-70. PubMed ID: 10744139
    [Abstract] [Full Text] [Related]

  • 36. Factor V Leiden and prothrombin gene G20210A mutations in Italian patients with Behçet's disease and deep vein thrombosis.
    Silingardi M, Salvarani C, Boiardi L, Accardo P, Iorio A, Olivieri I, Cantini F, Salvi F, La Corte R, Triolo G, Ciccia F, Ghirarduzzi A, Filippini D, Paolazzi G, Iori I.
    Arthritis Rheum; 2004 Apr 15; 51(2):177-83. PubMed ID: 15077257
    [Abstract] [Full Text] [Related]

  • 37. Hereditary angioedema associated with heterozygous factor V Leiden mutation in a patient with Purpura fulminans.
    Celikel S, Buyukasik Y, Karakaya G, Kalyoncu AF.
    Int Arch Allergy Immunol; 2007 Apr 15; 142(2):175-8. PubMed ID: 17068406
    [Abstract] [Full Text] [Related]

  • 38. The frequency of factor V Leiden and concomitance of factor V Leiden with prothrombin G20210A mutation and methylene tetrahydrofolate reductase C677T gene mutation in healthy population of Denizli, Aegean region of Turkey.
    Kabukcu S, Keskin N, Keskin A, Atalay E.
    Clin Appl Thromb Hemost; 2007 Apr 15; 13(2):166-71. PubMed ID: 17456626
    [Abstract] [Full Text] [Related]

  • 39. Anti-protein S antibodies following a varicella infection: detection, characterization and influence on thrombin generation.
    Regnault V, Boehlen F, Ozsahin H, Wahl D, de Groot PG, Lecompte T, de Moerloose P.
    J Thromb Haemost; 2005 Jun 15; 3(6):1243-9. PubMed ID: 15946215
    [Abstract] [Full Text] [Related]

  • 40. Prothrombin G20210A gene mutation with LightCycler polymerase chain reaction in venous thrombosis and healthy population in the southeast of Turkey.
    Ayyildiz O, Kalkanli S, Batun S, Aybak M, Isikdogan A, Tiftik N, Bolaman Z, Soker M, Muftuoglu E.
    Heart Vessels; 2004 Jul 15; 19(4):164-6. PubMed ID: 15278388
    [Abstract] [Full Text] [Related]

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