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Autor:
Fiona André, Martha Bujak, Nina Frischhut, Andreas Kronbichler, Norbert Sepp, Gudrun Ratzinger, Barbara Böckle
Publikováno v:
JEADV Clinical Practice, Vol 3, Iss 5, Pp 1478-1486 (2024)
Abstract Background Sjögren syndrome (SS) is a systemic autoimmune disease characterised by oral and ocular mucosal dryness. Objectives Our study focused on skin manifestations of SS. The differences between primary SS (pSS) and secondary SS (sSS) w
Externí odkaz:
https://doaj.org/article/6f2f90ce039945eaaed88971f7c7b7f9