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PUBMED FOR HANDHELDS

Journal Abstract Search


226 related items for PubMed ID: 3580299

  • 1. A new familial 'giant platelet syndrome' with structural, metabolic and functional abnormalities of platelets due to a primary megakaryocyte defect.
    Greaves M, Pickering C, Martin J, Cartwright I, Preston FE.
    Br J Haematol; 1987 Apr; 65(4):429-35. PubMed ID: 3580299
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  • 2. Bernard-Soulier syndrome: quantitative characterization of megakaryocytes and platelets by flow cytometric and platelet kinetic measurements.
    Tomer A, Scharf RE, McMillan R, Ruggeri ZM, Harker LA.
    Eur J Haematol; 1994 Apr; 52(4):193-200. PubMed ID: 8005229
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  • 3. Giant platelets, megakaryocytes and the expression of glycoprotein Ib-IX complexes.
    Nurden P, Nurden A.
    C R Acad Sci III; 1996 Aug; 319(8):717-26. PubMed ID: 8949396
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  • 4. Hereditary types of thrombocytopenia with giant platelets and inclusion bodies in the leukocytes.
    Greinacher A, Mueller-Eckhardt C.
    Blut; 1990 Feb; 60(2):53-60. PubMed ID: 2154271
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  • 5. [Hereditary hypogranular thrombocytopathic thrombocytopenia. Ultrastructural study of a megakaryocytopathy (author's transl)].
    Libánská J, Falcão L, Gautier A, Ammon J, Spahr A, Vainer H, Caen J.
    Nouv Rev Fr Hematol; 1975 Feb; 15(2):165-81. PubMed ID: 126429
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  • 6. Congenital disorders associated with platelet dysfunctions.
    Nurden P, Nurden AT.
    Thromb Haemost; 2008 Feb; 99(2):253-63. PubMed ID: 18278172
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  • 7. Megakaryocytes and inherited thrombocytopenias.
    Bellucci S.
    Baillieres Clin Haematol; 1997 Feb; 10(1):149-62. PubMed ID: 9154320
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  • 12. 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
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  • 13. Hereditary thrombocytopathy: a familial bleeding disorder due to impaired platelet coagulant activity.
    Ardlie NG, Coupland WW, Schoefl GI.
    Aust N Z J Med; 1976 Feb; 6(1):37-45. PubMed ID: 1065298
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  • 14. [Bernard-Soulier syndrome. An important differential diagnosis in chronic thrombocytopenia with bleeding complications].
    Greinacher A, Zellner A, Brangenberg R, Kiefel V, Mueller-Eckhardt C.
    Monatsschr Kinderheilkd; 1993 Jun; 141(6):483-6. PubMed ID: 8336744
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  • 15. Proplatelet formation in heterozygous Bernard-Soulier syndrome type Bolzano.
    Balduini A, Malara A, Pecci A, Badalucco S, Bozzi V, Pallotta I, Noris P, Torti M, Balduini CL.
    J Thromb Haemost; 2009 Mar; 7(3):478-84. PubMed ID: 19067792
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  • 16. Inherited thrombocytopenias: molecular mechanisms.
    Balduini CL, Savoia A.
    Semin Thromb Hemost; 2004 Oct; 30(5):513-23. PubMed ID: 15497094
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  • 17. Inherited giant platelet disorders. Classification and literature review.
    Mhawech P, Saleem A.
    Am J Clin Pathol; 2000 Feb; 113(2):176-90. PubMed ID: 10664620
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  • 19. Sustained thrombocytopenia in mice: serial studies of megakaryocytes and platelets.
    Stenberg PE, Levin J, Corash L.
    Exp Hematol; 1990 Feb; 18(2):124-32. PubMed ID: 2303104
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  • 20. Giant electron dense chains, clusters and granules in megakaryocytes and platelets with normal dense bodies: an inherited thrombocytopenic disorder IV. Ultrastructural cytochemistry and analytical electron microscopy.
    White JG, Ahlstrand GG.
    Platelets; 2003 Aug; 14(5):313-24. PubMed ID: 12944248
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