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Journal Abstract Search

209 related items for PubMed ID: 6495263

  • 21.
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  • 24. A missense mutation (Tyr88 to Cys) in the platelet membrane glycoprotein Ibbeta gene affects GPIb/IX complex expression--Bernard-Soulier syndrome in the homozygous form and giant platelets in the heterozygous form.
    Kurokawa Y, Ishida F, Kamijo T, Kunishima S, Kenny D, Kitano K, Koike K.
    Thromb Haemost; 2001 Nov; 86(5):1249-56. PubMed ID: 11816714
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  • 25. New morphological findings on platelets in Bernard-Soulier syndrome.
    Mori K, Suzuki S, Sugai K, Hisa S, Sakai H, Kobayashi Y.
    Tohoku J Exp Med; 1981 Apr; 133(4):479-80. PubMed ID: 7256741
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  • 26. The Bernard-Soulier syndrome: hereditary giant platelet disease.
    Jacobs P, Hougaard M, Bracher M, Hughes J.
    S Afr Med J; 1975 Nov 08; 49(47):1973-4. PubMed ID: 1198227
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  • 27. Platelet-vessel wall interaction: from the bedside to molecules.
    Caen JP, Rosa JP.
    Thromb Haemost; 1995 Jul 08; 74(1):18-24. PubMed ID: 8578453
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  • 28. Reevaluation of the presence of the major antigen Ca++ complex in Bernard-Soulier syndrome platelets. Elastase degradation of the complex in Bernard-Soulier syndrome platelet preparations.
    Shulman S, Wiesner R, Troll W, Karpatkin S.
    Thromb Res; 1983 Apr 01; 30(1):61-9. PubMed ID: 6190243
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  • 30. Bernard-Soulier syndrome in two Afrikaner families.
    Grové SS, Kromberg JG.
    S Afr Med J; 1985 Jun 29; 67(26):1050-2. PubMed ID: 4040267
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  • 32. Golgi complexes in hypogranular platelet syndromes.
    White JG.
    Platelets; 2005 Feb 29; 16(1):51-60. PubMed ID: 15763897
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  • 33. Platelets from "giant platelet syndrome (BSS)" are discocytes and normal sized.
    Frojmovic MM, Milton JG, Caen JP, Tobelem G.
    J Lab Clin Med; 1978 Jan 29; 91(1):109-16. PubMed ID: 618983
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  • 35. Bernard-Soulier syndrome: novel nonsense mutation in GPIbbeta gene affecting GPIb-IX complex expression.
    Hadjkacem B, Elleuch H, Gargouri J, Gargouri A.
    Ann Hematol; 2009 May 29; 88(5):465-72. PubMed ID: 18825380
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  • 36. Bernard-Soulier syndrome in pregnancy.
    Prabu P, Parapia LA.
    Clin Lab Haematol; 2006 Jun 29; 28(3):198-201. PubMed ID: 16706937
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  • 37. Novel point mutation in a leucine-rich repeat of the GPIbalpha chain of the platelet von Willebrand factor receptor, GPIb/IX/V, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: the N41H variant.
    Vettore S, Scandellari R, Moro S, Lombardi AM, Scapin M, Randi ML, Fabris F.
    Haematologica; 2008 Nov 29; 93(11):1743-7. PubMed ID: 18815197
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  • 39. Shape-changing agents produce abnormally large platelets in a hereditary "giant platelets syndrome (MPS)".
    Milton JG, Frojmovic MM.
    J Lab Clin Med; 1979 Jan 29; 93(1):154-61. PubMed ID: 759524
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  • 40. [Platelet shape in various clinical conditions. Its relation to the disease and significance (author's transl)].
    Hattori A, Sanada M, Kojima T, Ihzumi T, Shibata A.
    Nihon Ketsueki Gakkai Zasshi; 1979 Jun 29; 42(3):558-9. PubMed ID: 495020
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