Epstein-Barr Virus–Negative Granulomatous Disease Due to SAP Deficiency
Author:
Funder
Japan Society for the Promotion of Science
Publisher
Springer Science and Business Media LLC
Subject
Immunology,Immunology and Allergy
Link
https://link.springer.com/content/pdf/10.1007/s10875-021-01032-4.pdf
Reference6 articles.
1. Park JH, Levinson AI. Granulomatous-lymphocytic interstitial lung disease (GLILD) in common variable immunodeficiency (CVID). Clin Immunol. 2010;134(2):97–103. https://doi.org/10.1016/j.clim.2009.10.002.
2. Xu T, Zhao QQ, Li W, Chen X, Xue X, Chen Z, et al. X-linked lymphoproliferative syndrome in mainland China: review of clinical, genetic, and immunological characteristic. Eur J Pediatr. 2020;179(2):327–38. https://doi.org/10.1007/s00431-019-03512-7.
3. Kanegane H, Yang X, Zhao M, Yamato K, Inoue M, Hamamoto K, et al. Clinical features and outcome of X-linked lymphoproliferative syndrome type 1 (SAP deficiency) in Japan identified by the combination of flow cytometric assay and genetic analysis. Pediatr Allergy Immunol. 2012;23(5):488–93. https://doi.org/10.1111/j.1399-3038.2012.01282.x.
4. Booth C, Gilmour KC, Veys P, Gennery AR, Slatter MA, Chapel H, et al. X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease. Blood. 2011;117(1):53–62. https://doi.org/10.1182/blood-2010-06-284935.
5. Liu J, Tian W, Wang F, Teng W, Zhang Y, Tong C, et al. Maternal onset de novo SH2D1A mutation and lymphocytic choriomeningitis virus infection in a patient with X-linked lymphoproliferative disease type 1: a case report. Mol Med Rep. 2015;11(5):3291–4. https://doi.org/10.3892/mmr.2015.3173.
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