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Journal Abstract Search

151 related items for PubMed ID: 10605738

  • 1.
    ; . PubMed ID:
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  • 2. Inherited diseases of platelet glycoproteins: considerations for rapid molecular characterization.
    Bray PF.
    Thromb Haemost; 1994 Oct; 72(4):492-502. PubMed ID: 7878622
    [Abstract] [Full Text] [Related]

  • 3. Platelet-vessel wall interaction: from the bedside to molecules.
    Caen JP, Rosa JP.
    Thromb Haemost; 1995 Jul; 74(1):18-24. PubMed ID: 8578453
    [Abstract] [Full Text] [Related]

  • 4. Congenital disorders associated with platelet dysfunctions.
    Nurden P, Nurden AT.
    Thromb Haemost; 2008 Feb; 99(2):253-63. PubMed ID: 18278172
    [Abstract] [Full Text] [Related]

  • 5. Molecular pathology of the Bernard-Soulier syndrome, platelet-type von Willebrand's disease and Glanzmann's thrombasthenia.
    Clemetson KJ, Clemetson JM.
    Beitr Infusionsther; 1993 Feb; 31():168-73. PubMed ID: 7693249
    [No Abstract] [Full Text] [Related]

  • 6. Congenital disorders of platelet function.
    Rao AK, Holmsen H.
    Semin Hematol; 1986 Apr; 23(2):102-18. PubMed ID: 3010468
    [No Abstract] [Full Text] [Related]

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  • 8. Polymorphisms of human platelet membrane glycoproteins: structure and clinical significance.
    Nurden AT.
    Thromb Haemost; 1995 Jul; 74(1):345-51. PubMed ID: 8578482
    [Abstract] [Full Text] [Related]

  • 9.
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  • 10. Qualitative disorders of platelets and megakaryocytes.
    Nurden AT.
    J Thromb Haemost; 2005 Aug; 3(8):1773-82. PubMed ID: 16102044
    [Abstract] [Full Text] [Related]

  • 11. Are patients with Glanzmann thrombasthenia and the Bernard-Soulier syndrome protected against atherosclerosis?
    Nurden AT, Nurden P, George JN.
    Adv Exp Med Biol; 2001 Aug; 489():13-29. PubMed ID: 11554587
    [No Abstract] [Full Text] [Related]

  • 12. Inherited platelet disorders and oral health.
    Valera MC, Kemoun P, Cousty S, Sie P, Payrastre B.
    J Oral Pathol Med; 2013 Feb; 42(2):115-24. PubMed ID: 22583386
    [Abstract] [Full Text] [Related]

  • 13. [Constitutional thrombopathies: from the clinical description of rare diseases (Glanzmann thrombasthenia and Bernard-Soulier syndrome) to the development of new antithrombotic agents].
    Caen J, Bellucci S.
    Bull Acad Natl Med; 1998 Feb; 182(7):1493-502; discussion 1502-3. PubMed ID: 9916343
    [Abstract] [Full Text] [Related]

  • 14. Genetic testing in the diagnostic evaluation of inherited platelet disorders.
    Nurden AT, Fiore M, Pillois X, Nurden P.
    Semin Thromb Hemost; 2009 Mar; 35(2):204-12. PubMed ID: 19408193
    [Abstract] [Full Text] [Related]

  • 15. [Gene analysis of congenital platelet disorders].
    Tomiyama Y.
    Nihon Naika Gakkai Zasshi; 2000 Jun 10; 89(6):1093-9. PubMed ID: 10892183
    [No Abstract] [Full Text] [Related]

  • 16. Platelet receptor structures and polymorphisms.
    Kunicki TJ, Head S, Salomon DR.
    Methods Mol Biol; 2004 Jun 10; 273():455-78. PubMed ID: 15308818
    [No Abstract] [Full Text] [Related]

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  • 19. Platelet receptor polymorphisms and thrombotic risk.
    Santoso S, Kunicki T.
    Ital Heart J; 2001 Nov 10; 2(11):811-5. PubMed ID: 11770864
    [Abstract] [Full Text] [Related]

  • 20. Pseudo-Bernard-Soulier syndrome: thrombocytopenia caused by autoantibody to platelet glycoprotein Ib.
    Devine DV, Currie MS, Rosse WF, Greenberg CS.
    Blood; 1987 Aug 10; 70(2):428-31. PubMed ID: 3607280
    [Abstract] [Full Text] [Related]

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