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Autor:
M I Akaeva, D.V. Andzhelova, L V Sherstneva, E.E. Kazaryan, A M Kuchieva, N L Kozlovskaya, T V Smirnova, V.M. Sheludchenko, I A Velieva
Publikováno v:
Vestnik oftalmologii. 134(5. Vyp. 2)
The article presents a clinical observation of ocular thrombotic microangiopathy in atypical hemolytic-uremic syndrome - a rare genetic disease characterized by systemic thrombosis caused by uncontrolled activation of alternative complement pathway.