Zystische Nierenerkrankungen im Kindesalter
Author:
Publisher
Springer Berlin Heidelberg
Link
https://link.springer.com/content/pdf/10.1007/978-3-662-65248-0_26
Reference14 articles.
1. Bockenhauer D, Jaureguiberry G (2016) HNF1B-associated clinical phenotypes: the kidney and beyond. Pediatr Nephrol 31(5):707–714. https://doi.org/10.1007/s00467-015-3142-2
2. Burgmaier K, Kunzmann K, Ariceta G, Bergmann C, Buescher AK, Burgmaier M et al (2018) Risk factors for early dialysis dependency in autosomal recessive polycystic kidney disease. J Pediatr 199:22–28.e6. https://doi.org/10.1016/j.jpeds.2018.03.052
3. Burgmaier K, Ariceta G, Bald M, Buescher AK, Burgmaier M, Erger F et al (2020) Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD). Sci Rep 10(1):16025. https://doi.org/10.1038/s41598-020-71956-1
4. Cochat P, Febvey O, Bacchetta J, Bérard E, Cabrera N, Dubourg L (2019) Towards adulthood with a solitary kidney. Pediatr Nephrol 34(11):2311–2323. https://doi.org/10.1007/s00467-018-4085-1
5. Eickmeyer AB, Casanova NF, He C, Smith EA, Wan J, Bloom DA, Dillman JR (2014) The natural history of the multicystic dysplastic kidney–is limited follow-up warranted? J Pediatr Urol 10(4):655–661. https://doi.org/10.1016/j.jpurol.2014.06.001
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