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Journal Abstract Search

149 related items for PubMed ID: 34397000

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  • 2. Wiskott-Aldrich syndrome with macrothrombocytopenia.
    Skoric D, Dimitrijevic A, Cuturilo G, Ivanovski P.
    Indian Pediatr; 2014 Dec; 51(12):1015-6. PubMed ID: 25560165
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  • 4. Microthrombocytopenia in a male infant with cytomegalovirus.
    Krishnan KR, Vega R.
    Ann Allergy Asthma Immunol; 2009 Sep; 103(3):268-9. PubMed ID: 19788027
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  • 6. Clinical and genetic analysis of 2 rare cases of Wiskott-Aldrich syndrome from Chinese minorities: Two case reports.
    Liu H, Wang Y, Li Y, Tao L, Zhang Y, He X, Zhou Y, Liu X, Wang Y, Li L.
    Medicine (Baltimore); 2021 Apr 23; 100(16):e25527. PubMed ID: 33879693
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  • 7. A Clinical Diagnosis of Wiskott Aldrich Syndrome in an Ethiopian Boy with Recurrent Sinopulmonary Infections: A Case Report.
    Deribssa SJ, Alemayehu T.
    Ethiop J Health Sci; 2020 Nov 23; 30(6):1051-1054. PubMed ID: 33883853
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  • 9. [Wiskott-Aldrich syndrome].
    Gulácsy V, Maródi L.
    Orv Hetil; 2008 Jul 20; 149(29):1367-71. PubMed ID: 18617469
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  • 16. A novel mutation W252X in the WAS gene in a Korean patient with Wiskott-Aldrich syndrome.
    Kim HJ, Yoo EH, Ki CS, Yoo GH, Koo HH, Kim JW, Kim SH.
    Int J Hematol; 2006 Jun 20; 83(5):426-8. PubMed ID: 16787874
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  • 17. Wiskott-Aldrich syndrome: Two case reports with a novel mutation.
    Kamuran K, Çetin M, Geylan H, Karaman S, Demir N, Yurekturk E, Yavuz İ, Yavuz G, Tuncer O.
    Pediatr Hematol Oncol; 2017 Aug 20; 34(5):286-291. PubMed ID: 29200320
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  • 20. Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR.
    Proust A, Guillet B, Picard C, de Saint Basile G, Pondarré C, Tamary H, Dreyfus M, Tchernia G, Fischer A, Delaunay J.
    Blood Cells Mol Dis; 2007 Aug 20; 39(1):102-6. PubMed ID: 17400488
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