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Journal Abstract Search

286 related items for PubMed ID: 23033889

  • 1. Clinical and molecular characterization of Thai patients with Wiskott-Aldrich syndrome.
    Amarinthnukrowh P, Ittiporn S, Tongkobpetch S, Chatchatee P, Sosothikul D, Shotelersuk V, Suphapeetiporn K.
    Scand J Immunol; 2013 Jan; 77(1):69-74. PubMed ID: 23033889
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  • 2. Detection of six novel mutations in WASP gene in fifteen Iranian Wiskott-Aldrich patients.
    Safaei S, Fazlollahi MR, Houshmand M, Hamidieh AA, Bemanian MH, Alavi S, Mousavi F, Pourpak Z, Moin M.
    Iran J Allergy Asthma Immunol; 2012 Dec; 11(4):345-8. PubMed ID: 23264413
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  • 3. Wiskott-Aldrich syndrome; an x-linked primary immunodeficiency disease with unique and characteristic features.
    Ariga T.
    Allergol Int; 2012 Jun; 61(2):183-9. PubMed ID: 22361515
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  • 7. 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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  • 8. The genotype of the original Wiskott phenotype.
    Binder V, Albert MH, Kabus M, Bertone M, Meindl A, Belohradsky BH.
    N Engl J Med; 2006 Oct 26; 355(17):1790-3. PubMed ID: 17065640
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  • 9. Identification of six novel WASP gene mutations in patients suffering from Wiskott-Aldrich syndrome.
    Brooimans RA, van den Berg AJ, Tamminga RY, Revesz T, Wulffraat NM, Zegers BJ.
    Hum Mutat; 2000 Apr 26; 15(4):386-7. PubMed ID: 10737997
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  • 13. 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 26; 12(6):939-41. PubMed ID: 14612970
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  • 14. [Wiskott-Aldrich syndrome].
    Gulácsy V, Maródi L.
    Orv Hetil; 2008 Jul 20; 149(29):1367-71. PubMed ID: 18617469
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  • 15. A case of Wiskott-Aldrich syndrome with de novo mutation at exon 4.
    Doğu F, Ariga T, Ikincioğullari A, Bozdoğan G, Aytekin C, Metin A, Babacan E.
    Turk J Pediatr; 2006 Jul 20; 48(1):66-8. PubMed ID: 16562789
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  • 17. Identification of WASP mutations in 10 Australian families with Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
    Bourne HC, Weston S, Prasad M, Edkins E, Benson EM.
    Pathology; 2004 Jun 20; 36(3):262-4. PubMed ID: 15203732
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  • 18. Wiskott-Aldrich syndrome in Argentina: 17 unique, including nine novel, mutations.
    El-Hakeh J, Rosenzweig S, Oleastro M, Basack N, Berozdnik L, Molina F, Rivas EM, Zelazko M, Danielian S.
    Hum Mutat; 2002 Feb 20; 19(2):186-7. PubMed ID: 11793485
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  • 19. Molecular characterization of two Malaysian patients with Wiskott-Aldrich syndrome.
    Baharin MF, Kader Ibrahim SB, Yap SH, Abdul Manaf AM, Mat Ripen A, Dhaliwal JS.
    Malays J Pathol; 2015 Aug 20; 37(2):153-8. PubMed ID: 26277674
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  • 20. Wiskott-Aldrich syndrome iPS cells produce megakaryocytes with defects in cytoskeletal rearrangement and proplatelet formation.
    Ingrungruanglert P, Amarinthnukrowh P, Rungsiwiwut R, Maneesri-le Grand S, Sosothikul D, Suphapeetiporn K, Israsena N, Shotelersuk V.
    Thromb Haemost; 2015 Apr 20; 113(4):792-805. PubMed ID: 25518736
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