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Journal Abstract Search

127 related items for PubMed ID: 16209239

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  • 5. 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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  • 6. Wiskott-Aldrich syndrome: review of literature and report of case.
    Perino KE, James RB.
    J Oral Surg; 1980 Apr; 38(4):297-303. PubMed ID: 6928459
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  • 8. Management of Wiskott-Aldrich syndrome.
    Srivastava A, Swaid HA, Kabra M, Verma IC.
    Indian J Pediatr; 1996 Apr; 63(5):709-12. PubMed ID: 10830048
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  • 9. Current and emerging treatment options for Wiskott-Aldrich syndrome.
    Worth AJ, Thrasher AJ.
    Expert Rev Clin Immunol; 2015 Apr; 11(9):1015-32. PubMed ID: 26159751
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  • 14. 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
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  • 15. Wiskott-Aldrich syndrome.
    al Mulhim I.
    Indian Pediatr; 1995 Nov 01; 32(11):1224-8. PubMed ID: 8772876
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  • 16. [Wiskott-Aldrich syndrome: recent progress in diagnosis and treatment].
    Nonoyama S.
    Rinsho Ketsueki; 2009 Oct 01; 50(10):1570-6. PubMed ID: 19915368
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  • 17. Wiskott-Aldrich syndrome: diagnosis, clinical and laboratory manifestations, and treatment.
    Ochs HD, Filipovich AH, Veys P, Cowan MJ, Kapoor N.
    Biol Blood Marrow Transplant; 2009 Jan 01; 15(1 Suppl):84-90. PubMed ID: 19147084
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  • 18. The Wiskott-Aldrich syndrome.
    Ochs HD.
    Clin Rev Allergy Immunol; 2001 Feb 01; 20(1):61-86. PubMed ID: 11269229
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  • 19. [Wiskott-Aldrich syndrome. Recent information apropos of 4 cases].
    Griscelli C, Phan-Huu-Trung, Herzog C, Mozziconacci P.
    Nouv Rev Fr Hematol; 1973 Feb 01; 13(4):554-68. PubMed ID: 4271105
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  • 20. A Novel Mutation in a Child with Atypical Wiskott-Aldrich Syndrome Complicated by Cytomegalovirus Infection.
    Kaya Z, Muluk C, Hakoloğlu Ş, Tufan LŞ.
    Turk J Haematol; 2019 Feb 07; 36(1):70-71. PubMed ID: 29983408
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