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Autor:
V. N. Marchenko, E. A. Bruchkus, A. A. Lebedeva, D. A. Davydov, N. L. Shaporova, O. V. Dudina, O. A. Smul’skaya, M. K. Zinakova
Publikováno v:
Медицинская иммунология, Vol 22, Iss 2, Pp 383-392 (2020)
Eosinophilic granulomatosis with polyangiitis (EGPA), previously called Churg—Strauss syndrome, represents a rare form of ANCA-associated necrotising vasculitis which affects small vessels. This disease is characterized by typical combination of im
Externí odkaz:
https://doaj.org/article/1c89ad6d0c4f462da77115e0347432ce
