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Journal Abstract Search

302 related items for PubMed ID: 3535160

  • 1. Megakaryocytes from the marrow of a patient with Glanzmann's thrombasthenia lacked GP IIb-IIIa complexes.
    Hourdillé P, Fialon P, Belloc F, Namur M, Boisseau MR, Nurden AT.
    Thromb Haemost; 1986 Aug 20; 56(1):66-70. PubMed ID: 3535160
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  • 3. A variant of Glanzmann's thrombasthenia characterized by abnormal glycoprotein IIb/IIIa complex formation.
    Fournier DJ, Kabral A, Castaldi PA, Berndt MC.
    Thromb Haemost; 1989 Nov 24; 62(3):977-83. PubMed ID: 2512684
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  • 7. Role of platelet membrane glycoproteins Ib/IX and IIb/IIIa, and of platelet alpha-granule proteins in platelet aggregation induced by human osteosarcoma cells.
    Clezardin P, Drouin J, Morel-Kopp MC, Hanss M, Kehrel B, Serre CM, Kaplan C, Delmas PD.
    Cancer Res; 1993 Oct 01; 53(19):4695-700. PubMed ID: 7691402
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  • 10. [The immunodiagnosis of thrombocyte membrane glycoprotein deficiencies: Glanzmann's thrombasthenia, Bernard-Soulier syndrome and GMP-140 protein deficiency].
    Agafonova OG, Vinogradov DV, Khaspekova SG, Lagutina NIa, Labinskaia TA, Vasil'ev SA, Mazurov AV.
    Biull Eksp Biol Med; 1992 Dec 01; 114(12):635-7. PubMed ID: 1284039
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  • 11. Detection of carriers in Glanzmann's thrombasthenia.
    Zonneveld GT, van Leeuwen EF, Sturk A, ten Cate JW.
    Thromb Haemost; 1983 Jun 28; 49(3):182-6. PubMed ID: 6224309
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  • 12. Normal synthesis and expression of endothelial IIb/IIIa in Glanzmann's thrombasthenia.
    Giltay JC, Leeksma OC, Breederveld C, van Mourik JA.
    Blood; 1987 Mar 28; 69(3):809-12. PubMed ID: 3545321
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  • 14. Immunochemical evidence for protein abnormalities in platelets from patients with Glanzmann's thrombasthenia and Bernard-Soulier syndrome.
    Hagen I, Nurden A, Bjerrum OJ, Solum NO, Caen J.
    J Clin Invest; 1980 Mar 28; 65(3):722-31. PubMed ID: 7354135
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  • 15. [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 28; 37(12):1344-52. PubMed ID: 2614964
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  • 17. [The fluorescence flow cytometry technique in the diagnosis of hereditary platelet disorders--a case of Glanzmann's thrombasthenia].
    Holada K, Kruzík P, Mikolajová M, Rosipal S, Suttnar J, Kvasnicka J.
    Cas Lek Cesk; 1994 Dec 05; 133(23):734-6. PubMed ID: 7834672
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  • 18. [Familial occurrence of Glanzmann thrombasthenia].
    Musiał J, Krzanowski M, Judkiewicz L, Cierniewski C.
    Pol Tyg Lek; 1994 Dec 05; 47(5-6):138-40. PubMed ID: 1437802
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  • 19. Expression of the alloantigen Zwa (or P1A1) on human vascular smooth muscle cells and foreskin fibroblasts: a study on normal individuals and a patient with Glanzmann's thrombasthenia.
    Giltay JC, Brinkman HJ, von dem Borne AE, van Mourik JA.
    Blood; 1989 Aug 15; 74(3):965-70. PubMed ID: 2473812
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  • 20. Biochemical and molecular basis of Glanzmann's thrombasthenia.
    Perutelli P, Mori PG.
    Haematologica; 1992 Aug 15; 77(5):421-6. PubMed ID: 1483593
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