Lee WI - Search Results

1

Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination.

Imai K, Slupphaug G, Lee WI, Revy P, Nonoyama S, Catalan N, Yel L, Forveille M, Kavli B, Krokan HE, Ochs HD, Fischer A, Durandy A. Imai K, et al. Among authors: lee wi. Nat Immunol. 2003 Oct;4(10):1023-8. doi: 10.1038/ni974. Epub 2003 Sep 7. Nat Immunol. 2003. PMID: 12958596

2

Molecular analysis of a large cohort of patients with the hyper immunoglobulin M (IgM) syndrome.

Lee WI, Torgerson TR, Schumacher MJ, Yel L, Zhu Q, Ochs HD. Lee WI, et al. Blood. 2005 Mar 1;105(5):1881-90. doi: 10.1182/blood-2003-12-4420. Epub 2004 Sep 9. Blood. 2005. PMID: 15358621 Free article.

3

Inducible CO-stimulator molecule, a candidate gene for defective isotype switching, is normal in patients with hyper-IgM syndrome of unknown molecular diagnosis.

Lee WI, Zhu Q, Gambineri E, Jin Y, Welcher AA, Ochs HD. Lee WI, et al. J Allergy Clin Immunol. 2003 Nov;112(5):958-64. doi: 10.1016/s0091-6749(03)02021-9. J Allergy Clin Immunol. 2003. PMID: 14610488

4

Current Perspectives and Unmet Needs of Primary Immunodeficiency Care in Asia Pacific.

Leung D, Chua GT, Mondragon AV, Zhong Y, Nguyen-Ngoc-Quynh L, Imai K, Vignesh P, Suratannon N, Mao H, Lee WI, Kim YJ, Chan GCF, Liew WK, Huong LTM, Kanegane H, Muktiarti D, Zhao X, Santos-Ocampo FJ, Latiff AHA, Seger R, Ochs HD, Singh S, Lee PP, Lau YL. Leung D, et al. Among authors: lee pp, lee wi. Front Immunol. 2020 Aug 13;11:1605. doi: 10.3389/fimmu.2020.01605. eCollection 2020. Front Immunol. 2020. PMID: 32903579 Free PMC article.

5

X-linked hyper-immunoglobulin M syndrome: molecular genetic study and long-time follow-up of three generations of a Chinese family.

Lin SC, Shyur SD, Lee WI, Ma YC, Huang LH. Lin SC, et al. Among authors: lee wi. Int Arch Allergy Immunol. 2006;140(1):1-8. doi: 10.1159/000091744. Epub 2006 Feb 23. Int Arch Allergy Immunol. 2006. PMID: 16508335

6

Anti-IFN-γ autoantibodies are strongly associated with HLA-DR*15:02/16:02 and HLA-DQ*05:01/05:02 across Southeast Asia.

Ku CL, Lin CH, Chang SW, Chu CC, Chan JF, Kong XF, Lee CH, Rosen EA, Ding JY, Lee WI, Bustamante J, Witte T, Shih HP, Kuo CY, Chetchotisakd P, Kiertiburanakul S, Suputtamongkol Y, Yuen KY, Casanova JL, Holland SM, Doffinger R, Browne SK, Chi CY. Ku CL, et al. Among authors: lee ch, lee wi. J Allergy Clin Immunol. 2016 Mar;137(3):945-8.e8. doi: 10.1016/j.jaci.2015.09.018. Epub 2015 Oct 29. J Allergy Clin Immunol. 2016. PMID: 26522403 No abstract available.

7

Clinical aspects and genetic analysis of Taiwanese patients with the phenotype of hyper-immunoglobulin E recurrent infection syndromes (HIES).

Lee WI, Huang JL, Lin SJ, Yeh KW, Chen LC, Hsieh MY, Huang YC, Kuo HC, Yang KD, Yu HR, Jaing TH, Yang CH. Lee WI, et al. J Clin Immunol. 2011 Apr;31(2):272-80. doi: 10.1007/s10875-010-9479-1. Epub 2010 Dec 1. J Clin Immunol. 2011. PMID: 21120687

8

Analysis of genetic defects in patients with the common variable immunodeficiency phenotype in a single Taiwanese tertiary care hospital.

Lee WI, Huang JL, Kuo ML, Lin SJ, Chen LC, Chen MT, Jaing TH. Lee WI, et al. Ann Allergy Asthma Immunol. 2007 Nov;99(5):433-42. doi: 10.1016/S1081-1206(10)60569-8. Ann Allergy Asthma Immunol. 2007. PMID: 18051214

9

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. Lee WI, et al. J Clin Immunol. 2010 Jul;30(4):593-601. doi: 10.1007/s10875-010-9381-x. Epub 2010 Mar 16. J Clin Immunol. 2010. PMID: 20232122

10

De novo mutation causing X-linked hyper-IgM syndrome: a family study in Taiwan.

Ma YC, Lee WI, Shyur SD, Lin SC, Huang LH, Wu JY. Ma YC, et al. Among authors: lee wi. Asian Pac J Allergy Immunol. 2005 Mar;23(1):53-9. Asian Pac J Allergy Immunol. 2005. PMID: 15997875 Free article.

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