A rare cause of primary adrenal insufficiency due to a homozygous Arg188Cys mutation in the STAR gene

por Burget, Lukas, Parera, Laura Audí, Fernandez-Cancio, Monica, Gräni, Rolf, Henzen, Christoph, Flück, Christa E
Publicado 2018

Copeptin levels and commonly used laboratory parameters in hospitalised patients with severe hypernatraemia - the “Co-MED study”

por Nigro, Nicole, Winzeler, Bettina, Suter-Widmer, Isabelle, Schuetz, Philipp, Arici, Birsen, Bally, Martina, Refardt, Julie, Betz, Matthias, Gashi, Gani, Urwyler, Sandrine A., Burget, Lukas, Blum, Claudine A., Bock, Andreas, Huber, Andreas, Müller, Beat, Christ-Crain, Mirjam
Publicado 2018