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Journal Abstract Search

159 related items for PubMed ID: 16787874

  • 1. 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; 83(5):426-8. PubMed ID: 16787874
    [Abstract] [Full Text] [Related]

  • 2. 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; 37(2):153-8. PubMed ID: 26277674
    [Abstract] [Full Text] [Related]

  • 3. A novel WASP gene mutation in a Chinese boy with Wiskott-Aldrich syndrome.
    Yu H, Liu T, Meng W, Hou L.
    Int J Hematol; 2010 Sep; 92(2):271-5. PubMed ID: 20683686
    [Abstract] [Full Text] [Related]

  • 4. Novel WASP mutation in a patient with Wiskott-Aldrich syndrome: Case report and review of the literature.
    Eghbali M, Sadeghi-Shabestari M, Najmi Varzaneh F, Zare Bidoki A, Rezaei N.
    Allergol Immunopathol (Madr); 2016 Sep; 44(5):450-4. PubMed ID: 26993433
    [Abstract] [Full Text] [Related]

  • 5. Wiskott-Aldrich syndrome in a girl caused by heterozygous WASP mutation and extremely skewed X-chromosome inactivation: a novel association with maternal uniparental isodisomy 6.
    Takimoto T, Takada H, Ishimura M, Kirino M, Hata K, Ohara O, Morio T, Hara T.
    Neonatology; 2015 Sep; 107(3):185-90. PubMed ID: 25633059
    [Abstract] [Full Text] [Related]

  • 6. [Identification of two novel WASP gene mutations in 3 boys with Wiskott-Aldrich syndrome].
    Jiang LP, Xu YH, Yang XQ, Liu EM, Wang LJ, Lau YL, Chan KW.
    Zhonghua Er Ke Za Zhi; 2003 Aug; 41(8):590-3. PubMed ID: 14744380
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. 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 Dec; 48(1):66-8. PubMed ID: 16562789
    [Abstract] [Full Text] [Related]

  • 9. 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]

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

  • 11. Clinical aspects and genetic analysis of taiwanese patients with wiskott-Aldrich syndrome protein mutation: the first identification of x-linked thrombocytopenia in the chinese with novel mutations.
    Lee WI, Huang JL, Jaing TH, Wu KH, Chien YH, Chang KW.
    J Clin Immunol; 2010 Jul 23; 30(4):593-601. PubMed ID: 20232122
    [Abstract] [Full Text] [Related]

  • 12. [Mutation analysis of WASP gene and prenatal diagnosis of Wiskott-Aldrich syndrome].
    Liu N, Shi H, Kong X, Wu Q, Xu X, Bai Q, Feng Y, Zhao Z.
    Zhonghua Er Ke Za Zhi; 2014 Sep 23; 52(9):662-6. PubMed ID: 25476427
    [Abstract] [Full Text] [Related]

  • 13. 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 23; 58(2):297-9. PubMed ID: 22038941
    [Abstract] [Full Text] [Related]

  • 14. 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 23; 11(4):345-8. PubMed ID: 23264413
    [Abstract] [Full Text] [Related]

  • 15. Recurrent V75M mutation within the Wiskott-Aldrich syndrome protein: description of a homozygous female patient.
    Proust A, Guillet B, Pellier I, Rachieru P, Hoarau C, Claeyssens S, Léonard C, Charrier S, Vainchenker W, Tchernia G, Delaunay J.
    Eur J Haematol; 2005 Jul 23; 75(1):54-9. PubMed ID: 15946311
    [Abstract] [Full Text] [Related]

  • 16. A familial case of Wiskott-Aldrich Syndrome with a hotspot mutation in exon 2 of the WAS Gene.
    Park SK, Kim CS, Song DK, Kim JY, Choi IJ, Kim DK.
    J Korean Med Sci; 2007 Dec 23; 22(6):998-1001. PubMed ID: 18162713
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Wiskott-Aldrich syndrome with macrothrombocytopenia.
    Skoric D, Dimitrijevic A, Cuturilo G, Ivanovski P.
    Indian Pediatr; 2014 Dec 26; 51(12):1015-6. PubMed ID: 25560165
    [Abstract] [Full Text] [Related]

  • 19. 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 26; 34(5):286-291. PubMed ID: 29200320
    [Abstract] [Full Text] [Related]

  • 20. Clinical and molecular characteristics of Wiskott-Aldrich Syndrome in five unrelated Chinese families.
    Jiang J, Zhou J, Wei M, Singh S, Nikuze L, Huang L, Li Y, Jiang J, Wei H.
    Scand J Immunol; 2022 Jan 26; 95(1):e13115. PubMed ID: 34758123
    [Abstract] [Full Text] [Related]

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