Refine your research by the most used items
Author / Editor
- Ansermet, Camille (1)
- Auberson, Muriel (1)
- Baron, Roland (1)
- Bonny, Olivier (1)
- Centeno, Gabriel (1)
- Dirlewanger, Mijam (1)
- Firsov, Dmitri (1)
- Gautschi, Ivan (1)
- Girardin, Eric (1)
- Haenzi, Barbara (1)

Document type
Full text accessibility
Full text version
Subject
Highlights
Show items per page
Title | Authors / Editors | Date | |
---|---|---|---|
![]() |
Renal Fanconi Syndrome and Hypophosphatemic Rickets in the Absence of Xenotropic and Polytropic Retroviral Receptor in the Nephron | Ansermet, Camille; Moor, Matthias B.; Centeno, Gabriel; Auberson, Muriel; ... Firsov, Dmitri | 2017 |
![]() |
A homozygous missense mutation in SCNN1A is responsible for a transient neonatal form of pseudohypoaldosteronism type 1 | Dirlewanger, Mijam; Huser, Delphine; Zennaro, Maria-Christina; Girardin, Eric; ... Schwitzgebel Luscher, Valérie | 2011 |