Is autosomal dominant polycystic kidney disease an early sweet disease?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00467-021-05406-z.pdf
Reference84 articles.
1. Rowe I, Boletta A (2014) Defective metabolism in polycystic kidney disease: potential for therapy and open questions. Nephrol Dial Transplant 29:1480–1486. https://doi.org/10.1093/ndt/gft521
2. Rowe I, Chiaravalli M, Mannella V, Ulisse V et al (2013) Defective glucose metabolism in polycystic kidney disease identifies a new therapeutic strategy. Nat Med 19:488–493. https://doi.org/10.1038/nm.3092
3. Nowak KL, Hopp K (2020) Metabolic reprogramming in autosomal dominant polycystic kidney disease evidence and therapeutic potential. Clin J Am Soc Nephrol 15:577–584. https://doi.org/10.2215/CJN.13291019
4. Podrini C, Rowe I, Pagliarini R, Costa ASH et al (2018) Dissection of metabolic reprogramming in polycystic kidney disease reveals coordinated rewiring of bioenergetic pathways. Commun Biol 1:194. https://doi.org/10.1038/s42003-018-0200-x
5. Kipp KR, Rezaei M, Lin L, Dewey EC, Weimbs T (2016) A mild reduction of food intake slows disease progression in an orthologous mouse model of polycystic kidney disease. Am J Physiol Physiol 310:F726–F731. https://doi.org/10.1152/ajprenal.00551.2015
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5. Correction to: Is autosomal dominant polycystic kidney disease an early sweet disease?;Pediatric Nephrology;2022-06-21
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