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1.
Aschenbrenner, D.* et al.: Pathogenic interleukin-10 receptor alpha variants in humans - balancing natural selection and clinical implications. J. Clin. Immunol., DOI: 10.1007/s10875-022-01366-7 (2022)
2.
Schwierzeck, V. et al.: Molecular assessment of Staphylococcus Aureus strains in STAT3 Hyper-IgE syndrome patients. J. Clin. Immunol. 42, 1301-1309 (2022)
3.
Sefer, A.P.* et al.: Expanding the clinical and immunological phenotypes and natural history of MALT1 deficiency. J. Clin. Immunol. 42, 634-652 (2022)
4.
Lenz, D.* et al.: NBAS variants are associated with quantitative and qualitative NK and B cell deficiency. J. Clin. Immunol., DOI: 10.1007/s10875-021-01110-7 (2021)
5.
Daschkey, S.* et al.: Fatal lymphoproliferative disease in two siblings lacking functional FAAP24. J. Clin. Immunol. 36, 684-692 (2016)
6.
Poeck, H.* & Ruland, J.: ITAM receptor signaling and the NLRP3 inflammasome in antifungal immunity. J. Clin. Immunol. 30, 496-501 (2010)
7.
Hügle, B.* et al.: Persistent hypogammaglobulinemia following mononucleosis in boys is highly suggestive of X-linked lymphoproliferative disease--report of three cases. J. Clin. Immunol. 24, 515-522 (2005)
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