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Journal Abstract Search

194 related items for PubMed ID: 21382213

  • 21.
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  • 22. Genetic characteristics of eighty-seven patients with the Wiskott-Aldrich syndrome.
    Gulácsy V, Freiberger T, Shcherbina A, Pac M, Chernyshova L, Avcin T, Kondratenko I, Kostyuchenko L, Prokofjeva T, Pasic S, Bernatowska E, Kutukculer N, Rascon J, Iagaru N, Mazza C, Tóth B, Erdos M, van der Burg M, Maródi L, J Project Study Group.
    Mol Immunol; 2011 Feb; 48(5):788-92. PubMed ID: 21185603
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  • 23. 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; 30(6):1051-1054. PubMed ID: 33883853
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  • 27. A novel termination codon mutation of the WAS gene in a Thai family with Wiskott-Aldrich syndrome.
    Chatchatee P, Srichomthong C, Chewatavorn A, Shotelersuk V.
    Int J Mol Med; 2003 Dec; 12(6):939-41. PubMed ID: 14612970
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  • 29. Inherited thrombocytopenia, elevated serum IgA and renal disease: identification as a variant of the Wiskott-Aldrich syndrome.
    Standen GR, Lillicrap DP, Matthews N, Bloom AL.
    Q J Med; 1986 Apr; 59(228):401-8. PubMed ID: 3749445
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  • 30. [Wiskott-Aldrich syndrome with platelets of normal size and c.295C>T mutation of the WAS gene. Case report].
    Cunha-Carneiro ML, Xavier-Andrade M, Bacarini-Leite LF, Mosca T, Carvalho Neves Forte W.
    Rev Alerg Mex; 2023 Apr 19; 69(4):228-231. PubMed ID: 37218050
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  • 31.
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  • 32. [Wiskott-Aldrich syndrome: A case report and literature review].
    Liu YZ, Zhong Y, Wang YJ.
    Zhongguo Dang Dai Er Ke Za Zhi; 2006 Dec 19; 8(6):499-501. PubMed ID: 17178045
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  • 33. [A diagnostic approach for inherited thrombocytopenia].
    Pondarre C.
    Arch Pediatr; 2007 Jun 19; 14(6):676-8. PubMed ID: 17419013
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  • 34. [Wiskott-Aldrich syndrome in a hetrozygous woman].
    Tornai I, Kiss A, Laczkó J, Nagy PM.
    Orv Hetil; 1989 Mar 26; 130(13):679-82. PubMed ID: 2657554
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  • 35. Clinical, Laboratory Features and Clinical Courses of Patients with Wiskott Aldrich Syndrome and X-linked Thrombocytopenia-A single center study.
    Bildik HN, Cagdas D, Ozturk Kura A, Oskay Halacli S, Sanal O, Tezcan I.
    Immunol Invest; 2022 Jul 26; 51(5):1272-1283. PubMed ID: 34098853
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  • 39. [Analysis of clinical features and gene mutations in 6 patients with Wiskott-Aldrich syndrome].
    Jiang MH, Wang ZY, Su J, Cao LJ, Li JQ, Sun XH, Bai X, Wang GF, Ruan CG.
    Zhonghua Xue Ye Xue Za Zhi; 2011 Sep 26; 32(9):577-82. PubMed ID: 22338148
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