https://doi.org/10.1007/s10875-014-9989-3 ·
Journal: Journal of Clinical Immunology, 2014, №2, p.138-141
Publisher: Springer Science and Business Media LLC
Authors:
- Abbas Khalili
- Alessandro Plebani
- Massimiliano Vitali
- Hassan Abolhassani
- Vassilios Lougaris
- Babak Mirminachi
- Nima Rezaei
- Asghar Aghamohammadi
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https://doi.org/10.1007/s11882-008-0078-7
- Winkelstein JA, Marino MC, Lederman HM, Jones SM, Sullivan K, Burks AW, et al. X-linked agammaglobulinemia: report on a United States registry of 201 patients. Medicine. 2006;85(4):193–202. doi: 10.1097/01.md.0000229482.27398.ad .
https://doi.org/10.1097/01.md.0000229482.27398.ad
- Conley ME, Dobbs AK, Farmer DM, Kilic S, Paris K, Grigoriadou S, et al. Primary B cell immunodeficiencies: comparisons and contrasts. Annu Rev Immunol. 2009;27:199–227. doi: 10.1146/annurev.immunol.021908.132649 .
https://doi.org/10.1146/annurev.immunol.021908.132649
- Wang Y, Kanegane H, Sanal O, Tezcan I, Ersoy F, Futatani T, et al. Novel Igalpha (CD79a) gene mutation in a Turkish patient with B cell-deficient agammaglobulinemia. Am J Med Genet. 2002;108(4):333–6.
https://doi.org/10.1002/ajmg.10296
- Minegishi Y, Coustan-Smith E, Rapalus L, Ersoy F, Campana D, Conley ME. Mutations in Igalpha (CD79a) result in a complete block in B-cell development. J Clin Investig. 1999;104(8):1115–21. doi: 10.1172/JCI7696 .
https://doi.org/10.1172/JCI7696
- Bousfiha AA, Jeddane L, Ailal F, Al Herz W, Conley ME, Cunningham-Rundles C, et al. A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedside. J Clin Immunol. 2013;33(6):1078–87. doi: 10.1007/s10875-013-9901-6 .
https://doi.org/10.1007/s10875-013-9901-6
- Aghamohammadi A, Bahrami A, Mamishi S, Mohammadi B, Abolhassani H, Parvaneh N, et al. Impact of delayed diagnosis in children with primary antibody deficiencies. J Microbiol Immunol Infect. 2011;44(3):229–34. doi: 10.1016/j.jmii.2011.01.026 .
https://doi.org/10.1016/j.jmii.2011.01.026
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