Abstract Netherton syndrome is a rare and severe genodermatosis caused by pathogenic variants in SPINK5, leading to epidermal barrier dysfunction, immune dysregulation, and prominent atopic manifestations. Therapeutic options remain limited, and long-term real-world data on biologic treatment are scarce. We report a re...
Kamila Zawadzińska-Halat, Magdalena Stec, Katarzyna Poznańska-Kurowska et al.· Biologics : Targets & Therap...· 0 citations
HLA class II associations and metal–peptide–MHC/T-cell receptor interactions provide a plausible molecular basis for interindividual susceptibility, but available genetic data remain insufficient for clinical risk stratification or implant selection.
Nikodem Kuczyński, B. Szewczyk, M. Niedźwiedź et al.· International Journal of Mol...· 0 citations
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