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Journal Abstract Search

639 related items for PubMed ID: 21526886

  • 1. 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; 22(5):321-7. PubMed ID: 21526886
    [Abstract] [Full Text] [Related]

  • 2. 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; 24(6):613-8. PubMed ID: 23912132
    [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. Glanzmann's thrombasthenia in North Indians: sub classification and carrier detection by flow cytometry.
    Kannan M, Ahmad F, Yadav BK, Anand M, Jain P, Kumar R, Saxena R.
    Platelets; 2009 Feb; 20(1):12-5. PubMed ID: 19172516
    [Abstract] [Full Text] [Related]

  • 5. Evaluation of platelet surface glycoproteins in patients with Glanzmann thrombasthenia: Association with bleeding symptoms.
    Mutreja D, Sharma RK, Purohit A, Aggarwal M, Saxena R.
    Indian J Med Res; 2017 May; 145(5):629-634. PubMed ID: 28948953
    [Abstract] [Full Text] [Related]

  • 6. Identification of Clinicopathological Spectrum, Platelet Glycoprotein IIb/IIIa complex and Platelet Antibodies in Egyptian Children with Glanzmann's Thrombasthenia.
    Zahran AM, Saad K, Elsayh KI, Alblihed MA, Embaby M.
    Arch Immunol Ther Exp (Warsz); 2017 Dec; 65(6):565-571. PubMed ID: 28161816
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. [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]

  • 9. 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]

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

  • 11. Type I Glanzmann thrombasthenia: most common subtypes in North Indians.
    Kannan M, Ahmed RP, Jain P, Kumar R, Choudhry VP, Saxena R.
    Am J Hematol; 2003 Oct; 74(2):139-41. PubMed ID: 14508803
    [Abstract] [Full Text] [Related]

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

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

  • 14. Homozygous point mutations in platelet glycoprotein ITGA2B gene as cause of Glanzmann thrombasthenia in 2 families.
    Sandrock K, Halimeh S, Wiegering V, Kappert G, Sauer K, Deeg N, Busse E, Zieger B.
    Klin Padiatr; 2012 Apr; 224(3):174-8. PubMed ID: 22513797
    [Abstract] [Full Text] [Related]

  • 15. 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; 105(2):523-31. PubMed ID: 10233432
    [Abstract] [Full Text] [Related]

  • 16. Novel mutations of integrin αIIb and β3 genes in Turkish children with Glanzmann's thrombasthenia.
    Tokgoz H, Torun Ozkan D, Caliskan U, Akar N.
    Platelets; 2015 May; 26(8):779-82. PubMed ID: 25734216
    [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; 20(1):35-40. PubMed ID: 19172520
    [Abstract] [Full Text] [Related]

  • 18. A new case of acquired Glanzmann's thrombasthenia: diagnostic value of flow cytometry.
    Giannini S, Mezzasoma AM, Guglielmini G, Rossi R, Falcinelli E, Gresele P.
    Cytometry B Clin Cytom; 2008 May; 74(3):194-9. PubMed ID: 18200593
    [Abstract] [Full Text] [Related]

  • 19. Acquired Glanzmann's thrombasthenia caused by glycoprotein IIb/IIIa autoantibodies of the immunoglobulin G1 (IgG1), IgG2 or IgG4 subclass: a study in six cases.
    Porcelijn L, Huiskes E, Maatman R, de Kreuk A, de Haas M.
    Vox Sang; 2008 Nov; 95(4):324-30. PubMed ID: 19138263
    [Abstract] [Full Text] [Related]

  • 20. Human platelet alloantigen polymorphism in Glanzmann's thrombasthenia and its impact on the severity of the disease.
    Ghosh K, Kulkarni B, Nair S, Shetty S, Mohanty D.
    Br J Haematol; 2002 Nov; 119(2):348-53. PubMed ID: 12406067
    [Abstract] [Full Text] [Related]

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