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PUBMED FOR HANDHELDS

Journal Abstract Search


225 related items for PubMed ID: 7878622

  • 1. Inherited diseases of platelet glycoproteins: considerations for rapid molecular characterization.
    Bray PF.
    Thromb Haemost; 1994 Oct; 72(4):492-502. PubMed ID: 7878622
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  • 2. Molecular abnormalities in Glanzmann's thrombasthenia, Bernard-Soulier syndrome, and platelet-type von Willebrand's disease.
    Clemetson KJ, Clemetson JM.
    Curr Opin Hematol; 1994 Sep; 1(5):388-93. PubMed ID: 9371310
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  • 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
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  • 4. Identification of a homozygous single base pair deletion in the gene coding for the human platelet glycoprotein Ib alpha causing Bernard-Soulier syndrome.
    Simsek S, Admiraal LG, Modderman PW, van der Schoot CE, von dem Borne AE.
    Thromb Haemost; 1994 Sep; 72(3):444-9. PubMed ID: 7855797
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  • 8. The use of fluorescence flow cytometry in the characterization of Bernard-Soulier syndrome and Glanzmann's thrombasthenia.
    Fabris F, Casonato A, Randi ML, Luzzatto G, De Silvestro G, Ongaro G, Girolami A.
    Haematologica; 1989 Sep; 74(1):39-44. PubMed ID: 2498181
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  • 9. Are patients with Glanzmann thrombasthenia and the Bernard-Soulier syndrome protected against atherosclerosis?
    Nurden AT, Nurden P, George JN.
    Adv Exp Med Biol; 2001 Sep; 489():13-29. PubMed ID: 11554587
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  • 12. [Membrane glycoproteins of human platelets: structures, functions, and abnormalities in Glanzmann's thrombasthenia and Bernard-Soulier syndrome].
    Ando Y, Fusegawa H, Kawada T, Tanaka Y, Watanabe K, Kobayashi N.
    Rinsho Byori; 1989 Dec; 37(12):1344-52. PubMed ID: 2614964
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  • 15. [Analysis of Glanzmann's thrombasthenia and Bernard-Soulier syndrome using flow cytometry].
    Nomura S, Nagata H, Kitada T, Sone N, Oda K, Kokawa T, Yasunaga K, Nakajima T, Endo K.
    Rinsho Ketsueki; 1987 Mar; 28(3):377-85. PubMed ID: 3613125
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  • 17. Evidence that an abnormality in the glycoprotein Ib alpha gene is not the cause of abnormal platelet function in a family with classic Bernard-Soulier disease.
    Finch CN, Miller JL, Lyle VA, Handin RI.
    Blood; 1990 Jun 15; 75(12):2357-62. PubMed ID: 1972029
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