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342 related items for PubMed ID: 1483593

  • 1. Biochemical and molecular basis of Glanzmann's thrombasthenia.
    Perutelli P, Mori PG.
    Haematologica; 1992; 77(5):421-6. PubMed ID: 1483593
    [Abstract] [Full Text] [Related]

  • 2. [Glanzmann's thrombasthenia: a rare example of an integrin deficit].
    Perutelli P, Mori PG.
    Recenti Prog Med; 1992 Oct; 83(10):577-81. PubMed ID: 1462042
    [Abstract] [Full Text] [Related]

  • 3. Glanzmann's thrombasthenia: updated.
    Nair S, Ghosh K, Kulkarni B, Shetty S, Mohanty D.
    Platelets; 2002 Nov; 13(7):387-93. PubMed ID: 12487785
    [Abstract] [Full Text] [Related]

  • 4. A new variant of Glanzmann's thrombasthenia (Strasbourg I). Platelets with functionally defective glycoprotein IIb-IIIa complexes and a glycoprotein IIIa 214Arg----214Trp mutation.
    Lanza F, Stierlé A, Fournier D, Morales M, André G, Nurden AT, Cazenave JP.
    J Clin Invest; 1992 Jun; 89(6):1995-2004. PubMed ID: 1602006
    [Abstract] [Full Text] [Related]

  • 5. Classification of Iranian patients with Glanzmann's Thrombasthenia using a flow cytometric method.
    Farsinejad A, Abolghasemi H, Kazemi A, Aghaiipour M, Hadjati E, Faranoush M, Jazebi M, Ala F.
    Platelets; 2011 Jun; 22(5):321-7. PubMed ID: 21526886
    [Abstract] [Full Text] [Related]

  • 6. [Analysis of the GPIIb and GPIIIa genes in patients with Glanzmann's thrombasthenia].
    Yasunaga M, Ryo R, Adachi M, Sugano W, Yoshida A, Nakayama K, Saigo K, Yasunaga K, Yamaguchi N.
    Rinsho Ketsueki; 1992 Feb; 33(2):133-8. PubMed ID: 1635160
    [Abstract] [Full Text] [Related]

  • 7. A deletion in the gene for glycoprotein IIb associated with Glanzmann's thrombasthenia.
    Burk CD, Newman PJ, Lyman S, Gill J, Coller BS, Poncz M.
    J Clin Invest; 1991 Jan; 87(1):270-6. PubMed ID: 1702098
    [Abstract] [Full Text] [Related]

  • 8. Novel homozygous mutation (c.175delG) in platelet glycoprotein ITGA2B gene as cause of Glanzmann's thrombasthenia type I.
    Vannier C, Behnisch W, Bartsch I, Sandrock K, Ertle F, Schmidt K, Busse A, Superti-Furga A, Kulozik A, Santoso S, Zieger B.
    Klin Padiatr; 2010 May; 222(3):150-3. PubMed ID: 20514618
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. Application of GPIIIa gene Taq I polymorphism to determination of carrier status in Glanzmann's thrombasthenia families of Chinese origin.
    Ruan C, Gu J, Wang X, Chu X, Pan J.
    Thromb Haemost; 1993 Jan 11; 69(1):64-9. PubMed ID: 8095357
    [Abstract] [Full Text] [Related]

  • 11. Description of 10 new mutations in platelet glycoprotein IIb (alphaIIb) and glycoprotein IIIa (beta3) genes.
    Vinciguerra C, Bordet JC, Beaune G, Grenier C, Dechavanne M, Négrier C.
    Platelets; 2001 Dec 11; 12(8):486-95. PubMed ID: 11798398
    [Abstract] [Full Text] [Related]

  • 12. Abnormal processing of the glycoprotein IIb transcript due to a nonsense mutation in exon 17 associated with Glanzmann's thrombasthenia.
    Tomiyama Y, Kashiwagi H, Kosugi S, Shiraga M, Kanayama Y, Kurata Y, Matsuzawa Y.
    Thromb Haemost; 1995 May 11; 73(5):756-62. PubMed ID: 7482399
    [Abstract] [Full Text] [Related]

  • 13. Different biochemical expression pattern of platelet surface glycoproteins suggests molecular diversity of Glanzmann's thrombasthenia in Iran.
    Farsinejad A, Farajollahi MM, Kazemi A, Saemi N, Faranoush M.
    Blood Coagul Fibrinolysis; 2013 Sep 11; 24(6):613-8. PubMed ID: 23912132
    [Abstract] [Full Text] [Related]

  • 14. [Molecular pathology of inherited Glanzmann's thrombasthenia. Report of 11 cases].
    Ruan CG, Gu JM, Li JY.
    Zhonghua Nei Ke Za Zhi; 1992 Oct 11; 31(10):639-41, 659. PubMed ID: 1306460
    [Abstract] [Full Text] [Related]

  • 15. 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 11; 1(5):388-93. PubMed ID: 9371310
    [Abstract] [Full Text] [Related]

  • 16. Identification of an abnormal gene for the GPIIIa subunit of the platelet fibrinogen receptor resulting in Glanzmann's thrombasthenia.
    Bray PF, Shuman MA.
    Blood; 1990 Feb 15; 75(4):881-8. PubMed ID: 1967954
    [Abstract] [Full Text] [Related]

  • 17. Novel mutations in GP IIb gene in Glanzmann's thrombasthenia from India.
    Vijapurkar M, Ghosh K, Shetty S.
    Platelets; 2009 Feb 15; 20(1):35-40. PubMed ID: 19172520
    [Abstract] [Full Text] [Related]

  • 18. Clinical spectrum of Glanzmann's thrombasthenia.
    Badhe BA, Jayanthi S, Datta T.
    Indian J Pathol Microbiol; 2000 Jul 15; 43(3):297-302. PubMed ID: 11218676
    [Abstract] [Full Text] [Related]

  • 19. A Cys374Tyr homozygous mutation of platelet glycoprotein IIIa (beta 3) in a Chinese patient with Glanzmann's thrombasthenia.
    Grimaldi CM, Chen F, Scudder LE, Coller BS, French DL.
    Blood; 1996 Sep 01; 88(5):1666-75. PubMed ID: 8781422
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

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