The effect of autosomal dominant polycystic kidney disease on mucociliary clearance
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Otorhinolaryngology
Link
https://link.springer.com/content/pdf/10.1007/s00405-023-07891-4.pdf
Reference32 articles.
1. Ghata J, Cowley BD Jr (2011) Polycystic kidney disease. Compr Physiol. 7:945–975. https://doi.org/10.1002/cphy.c160018
2. Perumareddi P, Trelka DP (2020) Autosomal dominant polycystic kidney disease. Prim Care 47:673–689. https://doi.org/10.1016/j.pop.2020.08.010
3. Cornec-Le Gall E, Alam A, Perrone RD (2019) Autosomal dominant polycystic kidney disease. Lancet 393:919–935. https://doi.org/10.1016/S0140-6736(18)32782-X
4. Bergmann C (2019) Early and severe polycystic kidney disease and related Ciliopathies: an emerging field of interest. Nephron 141:50–60. https://doi.org/10.1159/000493532
5. Gimpel C, Bergmann C, Bockenhauer D et al (2019) International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people. Nat Rev Nephrol 15:713–726. https://doi.org/10.1038/s41581-019-0155-2
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