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189 related items for PubMed ID: 33879693

  • 1. 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]

  • 2. Report of clinical presentations and two novel mutations in patients with Wiskott-Aldrich syndrome/X-linked Thrombocytopenia.
    Udomkittivorakul N, Wattanasirichaigoon D, Manuyakorn W, Pongphitcha P, Khongkraparn A, Tunlayadechanont P, Sirachainan N.
    Platelets; 2022 Jul 04; 33(5):792-796. PubMed ID: 34705590
    [Abstract] [Full Text] [Related]

  • 3. 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 04; 30(4):593-601. PubMed ID: 20232122
    [Abstract] [Full Text] [Related]

  • 4. Wiskott-Aldrich syndrome/X-linked thrombocytopenia in China: Clinical characteristic and genotype-phenotype correlation.
    Liu DW, Zhang ZY, Zhao Q, Jiang LP, Liu W, Tu WW, Song WX, Zhao XD.
    Pediatr Blood Cancer; 2015 Sep 04; 62(9):1601-8. PubMed ID: 25931402
    [Abstract] [Full Text] [Related]

  • 5. 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 Sep 04; 39(1):102-6. PubMed ID: 17400488
    [Abstract] [Full Text] [Related]

  • 6. [Clinical features and genotype analysis of 132 patients with Wiskott-Aldrich syndrome].
    Li W, Liu D, Zhang X, Ding Y, Zhao X.
    Zhonghua Er Ke Za Zhi; 2015 Dec 04; 53(12):925-30. PubMed ID: 26887548
    [Abstract] [Full Text] [Related]

  • 7. 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 04; 51(5):1272-1283. PubMed ID: 34098853
    [Abstract] [Full Text] [Related]

  • 8. Identification of a Novel Gene Mutation in a Chinese Pedigree with X-linked Thrombocytopenia.
    Zhang JW, Luo YX, Yang YL, Long B, Lu Y, Zhang XZ.
    Clin Lab; 2018 Oct 31; 64(11):. PubMed ID: 30549999
    [Abstract] [Full Text] [Related]

  • 9. Disruption of hSWI/SNF complexes in T cells by WAS mutations distinguishes X-linked thrombocytopenia from Wiskott-Aldrich syndrome.
    Sarkar K, Sadhukhan S, Han SS, Vyas YM.
    Blood; 2014 Nov 27; 124(23):3409-19. PubMed ID: 25253772
    [Abstract] [Full Text] [Related]

  • 10. Intermittent low platelet counts hampering diagnosis of X-linked thrombocytopenia in children: report of two unrelated cases and a novel mutation in the gene coding for the Wiskott-Aldrich syndrome protein.
    Medina SS, Siqueira LH, Colella MP, Yamaguti-Hayakawa GG, Duarte BKL, Dos Santos Vilela MM, Ozelo MC.
    BMC Pediatr; 2017 Jun 22; 17(1):151. PubMed ID: 28641574
    [Abstract] [Full Text] [Related]

  • 11. [Genetic screening in early diagnosis of neonatal WAS gene-related disorders].
    Liu X, Yang L, Wang XC, Wu BB, Wang HJ, Wang HS, Qian XW, Cheng GQ, Cao Y, Sun JQ, Zhou WH.
    Zhonghua Er Ke Za Zhi; 2019 Jun 02; 57(6):429-433. PubMed ID: 31216799
    [Abstract] [Full Text] [Related]

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  • 14. 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 Jun 02; 44(5):450-4. PubMed ID: 26993433
    [Abstract] [Full Text] [Related]

  • 15. 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 02; 11(4):345-8. PubMed ID: 23264413
    [Abstract] [Full Text] [Related]

  • 16. A Novel Mutation Leading to Wiskott-Aldrich Syndrome in an Ethiopian Boy: a Case Report and a Review of Literature.
    Alemayehu T, Vinh DC.
    J Clin Immunol; 2023 Aug 02; 43(6):1272-1277. PubMed ID: 37052865
    [Abstract] [Full Text] [Related]

  • 17. 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 02; 92(2):271-5. PubMed ID: 20683686
    [Abstract] [Full Text] [Related]

  • 18. Wiskott-Aldrich syndrome with macrothrombocytopenia.
    Skoric D, Dimitrijevic A, Cuturilo G, Ivanovski P.
    Indian Pediatr; 2014 Dec 02; 51(12):1015-6. PubMed ID: 25560165
    [Abstract] [Full Text] [Related]

  • 19. 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 02; 30(6):1051-1054. PubMed ID: 33883853
    [Abstract] [Full Text] [Related]

  • 20. [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
    [Abstract] [Full Text] [Related]

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