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Journal Abstract Search

194 related items for PubMed ID: 21382213

  • 1. [Congenital thrombocytopenia in adults].
    van Zweeden A, Bot P, Smets Y, Terpstra W.
    Ned Tijdschr Geneeskd; 2011; 155():A2634. PubMed ID: 21382213
    [Abstract] [Full Text] [Related]

  • 2. Two novel mutations identified in the Wiskott-Aldrich syndrome protein gene cause Wiskott-Aldrich syndrome and thrombocytopenia.
    Andreu N, Matamoros N, Escudero A, Fillat C.
    Int J Mol Med; 2007 May; 19(5):777-82. PubMed ID: 17390083
    [Abstract] [Full Text] [Related]

  • 3. A unique presentation of Wiskott-Aldrich syndrome in relation to platelet size.
    Patel PD, Samanich JM, Mitchell WB, Manwani D.
    Pediatr Blood Cancer; 2011 Jul 01; 56(7):1127-9. PubMed ID: 21488158
    [Abstract] [Full Text] [Related]

  • 4. 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 Jul 01; 39(1):102-6. PubMed ID: 17400488
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  • 5. 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 01; 48(1):66-8. PubMed ID: 16562789
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  • 6. IVS6+5G>A found in Wiskott-Aldrich syndrome and X-linked thrombocytopenia in a Korean family.
    Yoon SH, Cho T, Kim HJ, Kim SY, Ko JH, Baek HS, Lee HJ, Lee CH.
    Pediatr Blood Cancer; 2012 Feb 01; 58(2):297-9. PubMed ID: 22038941
    [Abstract] [Full Text] [Related]

  • 7. [WASP gene mutation analysis of a family of X-linked thrombocytopenia].
    Shi RM, Liu ZG, Yang YH.
    Zhongguo Dang Dai Er Ke Za Zhi; 2010 Oct 01; 12(10):784-7. PubMed ID: 20959042
    [Abstract] [Full Text] [Related]

  • 8. Wiskott-Aldrich syndrome with macrothrombocytopenia.
    Skoric D, Dimitrijevic A, Cuturilo G, Ivanovski P.
    Indian Pediatr; 2014 Dec 01; 51(12):1015-6. PubMed ID: 25560165
    [Abstract] [Full Text] [Related]

  • 9. 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 01; 11(4):345-8. PubMed ID: 23264413
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Mutations of the WASP gene in 10 Japanese patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
    Itoh S, Nonoyama S, Morio T, Imai K, Okawa H, Ochs HD, Shimadzu M, Yata J.
    Int J Hematol; 2000 Jan 26; 71(1):79-83. PubMed ID: 10729999
    [Abstract] [Full Text] [Related]

  • 12. Two cases of Wiskott-Aldrich syndrome in neonates due to gene mutations.
    Zhang S, Zhang R, Chen C, Sun J.
    Fetal Pediatr Pathol; 2013 Jul 26; 32(4):312-5. PubMed ID: 23301916
    [Abstract] [Full Text] [Related]

  • 13. [The Wiskott-Aldrich syndrome in adulthood].
    Matzdorff A, Meindl A, Pralle H.
    Dtsch Med Wochenschr; 2000 Feb 11; 125(6):147-50. PubMed ID: 10700878
    [Abstract] [Full Text] [Related]

  • 14. Wiskott-Aldrich syndrome; an x-linked primary immunodeficiency disease with unique and characteristic features.
    Ariga T.
    Allergol Int; 2012 Jun 11; 61(2):183-9. PubMed ID: 22361515
    [Abstract] [Full Text] [Related]

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