Zobrazeno 1 - 1
of 1
pro vyhledávání: '"recombinant imiglucerase"'
Autor:
I. V. Lyagoskin, M. S. Pantyushenko, O. M. Strizhakova, N. K. Kudina, E. Yu. Prudnikova, P. V. Chichkanova, S. G. Abbasova
Publikováno v:
Биопрепараты: Профилактика, диагностика, лечение, Vol 20, Iss 1, Pp 42-49 (2020)
Enzyme replacement therapy (ERT) is one of the most efficient treatments for lysosomal storage diseases. Type 1 Gaucher disease is caused by β-glucocerebrosidase enzyme deficiency, which may be compensated for by intravenous infusions of imigluceras
Externí odkaz:
https://doaj.org/article/a507e5c6a71d4d2386c1c73253d6fa87
