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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; 22(5):321-7. PubMed ID: 21526886 [TBL] [Abstract][Full Text] [Related]
4. [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 [TBL] [Abstract][Full Text] [Related]
5. 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 [TBL] [Abstract][Full Text] [Related]
6. [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 [TBL] [Abstract][Full Text] [Related]
7. Biochemical and molecular basis of Glanzmann's thrombasthenia. Perutelli P; Mori PG Haematologica; 1992; 77(5):421-6. PubMed ID: 1483593 [TBL] [Abstract][Full Text] [Related]
8. Molecular abnormalities in Glanzmann's thrombasthenia, Bernard-Soulier syndrome, and platelet-type von Willebrand's disease. Clemetson KJ; Clemetson JM Curr Opin Hematol; 1994 Sep; 1(5):388-93. PubMed ID: 9371310 [TBL] [Abstract][Full Text] [Related]
9. Glanzmann's thrombasthenia (defective platelet integrin alphaIIb-beta3): proposals for management between evidence and open issues. Di Minno G; Coppola A; Di Minno MN; Poon MC Thromb Haemost; 2009 Dec; 102(6):1157-64. PubMed ID: 19967146 [TBL] [Abstract][Full Text] [Related]
10. Modulation of clinical phenotype of Glanzmann's thrombasthenia by thrombogenic mutations. Kannan M; Yadav BK; Ahmad F; Biswas A; Saxena R Clin Chim Acta; 2009 May; 403(1-2):156-8. PubMed ID: 19245802 [TBL] [Abstract][Full Text] [Related]
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13. A Cys374Tyr homozygous mutation of platelet glycoprotein IIIa (beta 3) in a Chinese patient with Glanzmann's thrombasthenia. Grimaldi CM; Chen F; Scudder LE; Coller BS; French DL Blood; 1996 Sep; 88(5):1666-75. PubMed ID: 8781422 [TBL] [Abstract][Full Text] [Related]
14. 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 [TBL] [Abstract][Full Text] [Related]
15. 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; 69(1):64-9. PubMed ID: 8095357 [TBL] [Abstract][Full Text] [Related]
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19. 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 [TBL] [Abstract][Full Text] [Related]
20. 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; 75(4):881-8. PubMed ID: 1967954 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]