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pro vyhledávání: '"Martin Siegenthaler"'
Autor:
Albina Nowak, Gilbert Koch, Uyen Huynh-Do, Martin Siegenthaler, Hans-Peter Marti, Marc Pfister
Publikováno v:
Kidney & Blood Pressure Research, Vol 42, Iss 1, Pp 1-15 (2017)
Background/Aims: Fabry disease (FD) is a rare inherited lysosomal storage disease with common and serious kidney complications. Enzyme replacement therapies (ERT) with agalsidase-α and -β were investigated to characterize their therapeutic effect o
Externí odkaz:
https://doaj.org/article/b8cd9f854ad947928b30c9f7fd23400d
Autor:
Martin Siegenthaler, Maas Ole Christopher, Frida Renstrom, Thomas Clerici, Flavio Forrer, Walter Kolb, Stefanie Sinz, Stefan Bilz
Publikováno v:
Endocrine Abstracts.
Publikováno v:
International journal of cardiology. 258