Polycystic Kidney Disease: ADPKD and ARPKD
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Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-11665-0_10
Reference198 articles.
1. Bergmann C, Guay-Woodford LM, Harris PC, et al. Polycystic kidney disease. Nat Rev Dis Primer. 2018;4:50. https://doi.org/10.1038/s41572-018-0047-y.
2. De Rechter S, Bammens B, Schaefer F, et al. Unmet needs and challenges for follow-up and treatment of autosomal dominant polycystic kidney disease: the paediatric perspective. Clin Kidney J. 2018;11:i14–26. https://doi.org/10.1093/ckj/sfy088.
3. Burgmaier K, Kilian S, Bammens B, et al. Clinical courses and complications of young adults with autosomal recessive polycystic kidney disease (ARPKD). Sci Rep. 2019;9:7919. https://doi.org/10.1038/s41598-019-43488-w.
4. Liebau MC. Early clinical management of autosomal recessive polycystic kidney disease. Pediatr Nephrol Berl Ger. 2021;36:3561–70. https://doi.org/10.1007/s00467-021-04970-8.
5. Osathanondh V, Potter EL. Pathogenesis of polycystic kidneys. Type 4 due to urethral obstruction. Arch Pathol. 1964;77:502–9.
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