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Journal Abstract Search

320 related items for PubMed ID: 19172520

  • 1. 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]

  • 2. 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
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  • 3. 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 May; 22(5):321-7. PubMed ID: 21526886
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  • 4. Role of RFLP using TspRI for carrier detection in Glanzmann's thrombasthenia: a report on two families.
    Kannan M, Yadav BK, Ahmad F, Saxena R.
    Int J Lab Hematol; 2010 Feb; 32(1 Pt 1):e158-62. PubMed ID: 19170775
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  • 5. Glanzmann's thrombasthenia: identification of 19 new mutations in 30 patients.
    D'Andrea G, Colaizzo D, Vecchione G, Grandone E, Di Minno G, Margaglione M, GLAnzmann's Thrombasthenia Italian Team (GLATIT).
    Thromb Haemost; 2002 Jun; 87(6):1034-42. PubMed ID: 12083483
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  • 6. 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; 12(8):486-95. PubMed ID: 11798398
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  • 7. 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 Dec; 26(8):779-82. PubMed ID: 25734216
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  • 11. 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
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  • 12. 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
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  • 13. Nonsense mutation in exon-19 of GPIIb associated with thrombasthenic phenotype. Failure of GPIIb(delta597-1008) to form stable complexes with GPIIIa.
    Arias-Salgado EG, Tao J, González-Manchón C, Butta N, Vicente V, Ayuso MS, Parrilla R.
    Thromb Haemost; 2002 Apr; 87(4):684-91. PubMed ID: 12008952
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  • 14. Glanzmann's thrombasthenia: updated.
    Nair S, Ghosh K, Kulkarni B, Shetty S, Mohanty D.
    Platelets; 2002 Nov; 13(7):387-93. PubMed ID: 12487785
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  • 15. [Novel frame-shift mutation of 540 A deletion in GP IIb gene from a patient with Glanzmann thrombasthenia].
    Jian ZF, Tang FQ, Chen FP, Xie QZ, Wang GP.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2008 Feb; 33(2):165-8. PubMed ID: 18326913
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  • 16. Biochemical and molecular basis of Glanzmann's thrombasthenia.
    Perutelli P, Mori PG.
    Haematologica; 1992 Feb; 77(5):421-6. PubMed ID: 1483593
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  • 17. Prenatal diagnosis of Glanzmann thrombasthenia.
    Srivastava A, Usher S, Nelson EJ, Jayandharan G, Shaji RV, Chandy M, Seligsohn U, Peretz H.
    Natl Med J India; 2003 Feb; 16(4):207-8. PubMed ID: 14606769
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  • 20. 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; 73(5):756-62. PubMed ID: 7482399
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