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Journal Abstract Search

112 related items for PubMed ID: 8156036

  • 21. 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]

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

  • 23.
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  • 24. The use of fluorescence flow cytometry in the characterization of Bernard-Soulier syndrome and Glanzmann's thrombasthenia.
    Fabris F, Casonato A, Randi ML, Luzzatto G, De Silvestro G, Ongaro G, Girolami A.
    Haematologica; 1989 Feb; 74(1):39-44. PubMed ID: 2498181
    [Abstract] [Full Text] [Related]

  • 25. Molecular pathology of the Bernard-Soulier syndrome, platelet-type von Willebrand's disease and Glanzmann's thrombasthenia.
    Clemetson KJ, Clemetson JM.
    Beitr Infusionsther; 1993 Feb; 31():168-73. PubMed ID: 7693249
    [No Abstract] [Full Text] [Related]

  • 26. Functional platelet defects and their laboratory evaluation.
    Bowie EJ, Owen CA.
    Southeast Asian J Trop Med Public Health; 1979 Jun; 10(2):234-40. PubMed ID: 524147
    [Abstract] [Full Text] [Related]

  • 27. Factor X deficiency in North Pakistan.
    Anwar M, Hamdani SN, Ayyub M, Ali W.
    J Ayub Med Coll Abbottabad; 2004 Jun; 16(3):1-4. PubMed ID: 15631360
    [Abstract] [Full Text] [Related]

  • 28. 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]

  • 29. Bone marrow transplantation in severe Glanzmann's thrombasthenia with antiplatelet alloimmunization.
    Bellucci S, Damaj G, Boval B, Rocha V, Devergie A, Yacoub-Agha I, Garderet L, Ribaud P, Traineau R, Socié G, Gluckman E.
    Bone Marrow Transplant; 2000 Feb; 25(3):327-30. PubMed ID: 10673707
    [Abstract] [Full Text] [Related]

  • 30. [Glanzmann's thrombasthenia. Apropos of 22 cases].
    Meddeb B, Ben Abid H, Hafsia R, Hafsia A, Khaier R, Ben Hafsa R.
    Tunis Med; 1986 Jan; 64(1):29-34. PubMed ID: 3715990
    [No Abstract] [Full Text] [Related]

  • 31. Inherited disorders of platelet function in pediatric clinical practice: a diagnostic challenge.
    Streif W, Knöfler R, Eberl W.
    Klin Padiatr; 2010 May; 222(3):203-8. PubMed ID: 20514633
    [Abstract] [Full Text] [Related]

  • 32.
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  • 33. 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
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  • 35. Inherited bleeding syndromes in Iraq.
    Al-Mondhiry HA.
    Thromb Haemost; 1977 Jun 30; 37(3):549-55. PubMed ID: 302041
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  • 37. Congenital disorders of platelet function.
    Rao AK.
    Hematol Oncol Clin North Am; 1990 Feb 30; 4(1):65-86. PubMed ID: 2155905
    [Abstract] [Full Text] [Related]

  • 38. [Glanzmann's thrombasthenia: first case descriptions in sub-Saharan Africa].
    Dokekias AE, Galiba FO, Koko I.
    Tunis Med; 2008 Aug 30; 86(8):761-3. PubMed ID: 19472764
    [Abstract] [Full Text] [Related]

  • 39. [Glanzmann's disease: diagnostic study of 6 patients].
    Quiroga T, Mezzano D, Aranda E, Montesinos M, Foradori A, Bull P, Schuh W, Morales M, Vargas L.
    Rev Med Chil; 1985 Nov 30; 113(11):1076-83. PubMed ID: 3879773
    [No Abstract] [Full Text] [Related]

  • 40. [Membrane glycoproteins of human platelets: structures, functions, and abnormalities in Glanzmann's thrombasthenia and Bernard-Soulier syndrome].
    Ando Y, Fusegawa H, Kawada T, Tanaka Y, Watanabe K, Kobayashi N.
    Rinsho Byori; 1989 Dec 30; 37(12):1344-52. PubMed ID: 2614964
    [Abstract] [Full Text] [Related]

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