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158 related items for PubMed ID: 33957723

  • 1. Flow cytometric analysis of platelet surface glycoproteins in the diagnosis of thirty-two Turkish patients with Glanzmann thrombasthenia: a multicenter experience.
    Saraymen B, Muhtaroğlu S, Köker MY, Sarper N, Zengin E, Albayrak C, Albayrak D, Zülfikar B, Koç Şenol B, Bentli E, Yılmaz S, Çetin A, Eser B, Çetin M.
    Turk J Med Sci; 2021 Aug 30; 51(4):2135-2141. PubMed ID: 33957723
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  • 2. 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 30; 145(5):629-634. PubMed ID: 28948953
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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 30; 22(5):321-7. PubMed ID: 21526886
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  • 4. Diagnosis of Glanzmann thrombasthenia by whole blood impedance analyzer (MEA) vs. light transmission aggregometry.
    Albanyan A, Al-Musa A, AlNounou R, Al Zahrani H, Nasr R, AlJefri A, Saleh M, Malik A, Masmali H, Owaidah T.
    Int J Lab Hematol; 2015 Aug 30; 37(4):503-8. PubMed ID: 25537026
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  • 6. Two homozygous missense mutations in ITGB3 gene as a cause of Glanzmann Thrombasthenia in four consanguineous Pakistani pedigrees.
    Ali T, Gul S, Amar A, Shakoor M, Farhan S, Mohsin S, Khaliq S.
    Int J Lab Hematol; 2020 Oct 30; 42(5):628-635. PubMed ID: 32558238
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  • 7. 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 30; 74(2):139-41. PubMed ID: 14508803
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  • 12. A point mutation in the cysteine-rich domain of glycoprotein (GP) IIIa results in the expression of a GPIIb-IIIa (alphaIIbbeta3) integrin receptor locked in a high-affinity state and a Glanzmann thrombasthenia-like phenotype.
    Ruiz C, Liu CY, Sun QH, Sigaud-Fiks M, Fressinaud E, Muller JY, Nurden P, Nurden AT, Newman PJ, Valentin N.
    Blood; 2001 Oct 15; 98(8):2432-41. PubMed ID: 11588040
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  • 13. Identification of one novel pathogenic ITGB3 mutation and two known mutations in two Chinese pedigrees with hereditary Glanzmann thrombasthenia.
    Lu Z, Nikuze L, Zhong Z, Li F, Zhang F, Liang K, Wei M, Wei H.
    Platelets; 2020 Oct 15; 31(3):355-359. PubMed ID: 31088191
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  • 15. Glanzmann thrombasthenia: genetic basis and clinical correlates.
    Botero JP, Lee K, Branchford BR, Bray PF, Freson K, Lambert MP, Luo M, Mohan S, Ross JE, Bergmeier W, Di Paola J, ClinGen Platelet Disorder Variant Curation Expert Panel.
    Haematologica; 2020 Apr 15; 105(4):888-894. PubMed ID: 32139434
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  • 16. Diversity of Glanzmann thrombasthenia in southern India: 10 novel mutations identified among 15 unrelated patients.
    Nelson EJ, Nair SC, Peretz H, Coller BS, Seligsohn U, Chandy M, Srivastava A.
    J Thromb Haemost; 2006 Aug 15; 4(8):1730-7. PubMed ID: 16879215
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  • 18. Immunization against αIIb β3 and αv β3 in Glanzmann thrombasthenia patients carrying the French Gypsy mutation.
    Fiore M, Bayat B, Phuangtham R, Blouin L, Huguenin Y, Bein G, Santoso S.
    J Thromb Haemost; 2021 Jan 15; 19(1):255-261. PubMed ID: 33090654
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