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Journal Abstract Search

342 related items for PubMed ID: 1483593

  • 21. [Familial occurrence of Glanzmann thrombasthenia].
    Musiał J, Krzanowski M, Judkiewicz L, Cierniewski C.
    Pol Tyg Lek; ; 47(5-6):138-40. PubMed ID: 1437802
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  • 23. Glanzmann's thrombasthenia associated with deletion-insertion and alternative splicing in the glycoprotein IIb gene.
    Peretz H, Rosenberg N, Usher S, Graff E, Newman PJ, Coller BS, Seligsohn U.
    Blood; 1995 Jan 15; 85(2):414-20. PubMed ID: 7529063
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  • 24. Glanzmann's thrombasthenia: an overview.
    Kannan M, Saxena R.
    Clin Appl Thromb Hemost; 2009 Jan 15; 15(2):152-65. PubMed ID: 18930954
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  • 25. [Platelet aggregations and glycoproteins].
    Yamamoto N, Arai M, Tanoue K.
    Rinsho Byori; 1992 Mar 15; 40(3):272-81. PubMed ID: 1518178
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  • 26. Asialo von Willebrand factor interactions with platelets. Interdependence of glycoproteins Ib and IIb/IIIa for binding and aggregation.
    Grainick HR, Williams SB, Coller BS.
    J Clin Invest; 1985 Jan 15; 75(1):19-25. PubMed ID: 2981249
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  • 29. A variant of Glanzmann's thrombasthenia with abnormal glycoprotein IIb-IIIa complexes in the platelet membrane.
    Nurden AT, Rosa JP, Fournier D, Legrand C, Didry D, Parquet A, Pidard D.
    J Clin Invest; 1987 Mar 15; 79(3):962-9. PubMed ID: 3818957
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  • 31. Characterization of an antibody to the integrin beta 3 subunit (GP IIIa) from a patient with neonatal thrombocytopenia and an inherited deficiency of GP IIb-IIIa complexes in platelets (Glanzmann's thrombasthenia).
    Jallu V, Pico M, Chevaleyre J, Vézon G, Kunicki TJ, Nurden AT.
    Hum Antibodies Hybridomas; 1992 Apr 15; 3(2):93-106. PubMed ID: 1633270
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  • 32. Diagnosis of Glanzmann's thrombasthenia and carrier detection using monoclonal antibodies to platelet glycoprotein IIb and IIIa in immunoblotting.
    Perutelli P, Marchese P, Mori PG.
    Haemostasis; 1992 Apr 15; 22(6):330-3. PubMed ID: 1478543
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  • 33. 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 15; 105(2):523-31. PubMed ID: 10233432
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  • 34. Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism.
    D'Andrea G, Margaglione M, Glansmann's Thrombasthemia Italian Team (GLATIT).
    Haematologica; 2003 Dec 15; 88(12):1378-82. PubMed ID: 14687991
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  • 35. 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
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  • 36. A 1063G-->A mutation in exon 12 of glycoprotein (GP)IIb associated with a thrombasthenic phenotype: mutation analysis of [324E]GPIIb.
    Tao J, Arias-Salgado EG, González-Manchón C, Iruín G, Butta N, Ayuso MS, Parrilla R.
    Br J Haematol; 2000 Dec 15; 111(3):965-73. PubMed ID: 11122161
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  • 37. A three amino acid deletion in glycoprotein IIIa is responsible for type I Glanzmann's thrombasthenia: importance of residues Ile325Pro326Gly327 for beta3 integrin subunit association.
    Morel-Kopp MC, Kaplan C, Proulle V, Jallu V, Melchior C, Peyruchaud O, Aurousseau MH, Kieffer N.
    Blood; 1997 Jul 15; 90(2):669-77. PubMed ID: 9226167
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  • 38. [Constitutional thrombopathies: from the clinical description of rare diseases (Glanzmann thrombasthenia and Bernard-Soulier syndrome) to the development of new antithrombotic agents].
    Caen J, Bellucci S.
    Bull Acad Natl Med; 1998 Jul 15; 182(7):1493-502; discussion 1502-3. PubMed ID: 9916343
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  • 39. Stimulated Glanzmann's thrombasthenia platelets produced microvesicles. Microvesiculation correlates better to exposure of procoagulant surface than to activation of GPIIb-IIIa.
    Holme PA, Solum NO, Brosstad F, Egberg N, Lindahl TL.
    Thromb Haemost; 1995 Dec 15; 74(6):1533-40. PubMed ID: 8772233
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  • 40. 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
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