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182 related items for PubMed ID: 1635160

  • 1. [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]

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

  • 3. 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]

  • 4. Biochemical and molecular basis of Glanzmann's thrombasthenia.
    Perutelli P, Mori PG.
    Haematologica; 1992 Jan 11; 77(5):421-6. PubMed ID: 1483593
    [Abstract] [Full Text] [Related]

  • 5. 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 11; 87(1):270-6. PubMed ID: 1702098
    [Abstract] [Full Text] [Related]

  • 6. [Glanzmann's thrombasthenia: a rare example of an integrin deficit].
    Perutelli P, Mori PG.
    Recenti Prog Med; 1992 Oct 11; 83(10):577-81. PubMed ID: 1462042
    [Abstract] [Full Text] [Related]

  • 7. Glanzmann's thrombasthenia: updated.
    Nair S, Ghosh K, Kulkarni B, Shetty S, Mohanty D.
    Platelets; 2002 Nov 11; 13(7):387-93. PubMed ID: 12487785
    [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 11; 222(3):150-3. PubMed ID: 20514618
    [Abstract] [Full Text] [Related]

  • 9. [Carrier detection of Glanzmann's thrombasthenia by Taq I restriction fragment length polymorphism of GPIIIa gene].
    Gu J.
    Zhonghua Yi Xue Za Zhi; 1991 Dec 11; 71(12):680-2, 46. PubMed ID: 1687449
    [Abstract] [Full Text] [Related]

  • 10. 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 Dec 11; 22(5):321-7. PubMed ID: 21526886
    [Abstract] [Full Text] [Related]

  • 11. Homozygous Cys542-->Arg substitution in GPIIIa in a Swiss patient with type I Glanzmann's thrombasthenia.
    Ruan J, Schmugge M, Clemetson KJ, Cazes E, Combrie R, Bourre F, Nurden AT.
    Br J Haematol; 1999 May 11; 105(2):523-31. PubMed ID: 10233432
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. 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 15; 73(5):756-62. PubMed ID: 7482399
    [Abstract] [Full Text] [Related]

  • 14. Glanzmann's thrombasthenia: an overview.
    Kannan M, Saxena R.
    Clin Appl Thromb Hemost; 2009 May 15; 15(2):152-65. PubMed ID: 18930954
    [Abstract] [Full Text] [Related]

  • 15. Molecular basis for Glanzmann's thrombasthenia (GT) in a compound heterozygote with glycoprotein IIb gene: a proposal for the classification of GT based on the biosynthetic pathway of glycoprotein IIb-IIIa complex.
    Kato A, Yamamoto K, Miyazaki S, Jung SM, Moroi M, Aoki N.
    Blood; 1992 Jun 15; 79(12):3212-8. PubMed ID: 1317725
    [Abstract] [Full Text] [Related]

  • 16. [Rapid detection of platelet glycoprotein IIb, IIIA gene variety by single strand conformation polymorphism analysis].
    Chen F, Coller B, French D.
    Zhonghua Yi Xue Za Zhi; 1995 Jun 15; 75(6):341-3, 382. PubMed ID: 7553144
    [Abstract] [Full Text] [Related]

  • 17. 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 15; 24(6):613-8. PubMed ID: 23912132
    [Abstract] [Full Text] [Related]

  • 18. An exon 28 mutation resulting in alternative splicing of the glycoprotein IIb transcript and Glanzmann's thrombasthenia.
    Iwamoto S, Nishiumi E, Kajii E, Ikemoto S.
    Blood; 1994 Feb 15; 83(4):1017-23. PubMed ID: 8111043
    [Abstract] [Full Text] [Related]

  • 19. 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 15; 12(8):486-95. PubMed ID: 11798398
    [Abstract] [Full Text] [Related]

  • 20. Mutations in the alphaIIb and beta3 genes that cause Glanzmann thrombasthenia can be distinguished by a simple procedure using transformed B-lymphocytes.
    Rosenberg N, Dardik R, Rosenthal E, Zivelin A, Seligsohn U.
    Thromb Haemost; 1998 Feb 15; 79(2):244-8. PubMed ID: 9493569
    [Abstract] [Full Text] [Related]

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