Defective glycolysis and the use of 2-deoxy-d-glucose in polycystic kidney disease: from animal models to humans
Author:
Funder
Ministero della Salute
PKD Foundation
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
http://link.springer.com/article/10.1007/s40620-017-0395-9/fulltext.html
Reference65 articles.
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2. Willey CJ, Blais JD, Hall AK, Krasa HB, Makin AJ, Czerwiec FS (2016) Prevalence of autosomal dominant polycystic kidney disease in the European Union. Nephrol Dial Transplant. doi: 10.1093/ndt/gfw240
3. Ong AC, Devuyst O, Knebelmann B, Walz G, Diseases E-EWGfIK (2015) Autosomal dominant polycystic kidney disease: the changing face of clinical management. Lancet 385(9981):1993–2002. doi: 10.1016/S0140-6736(15)60907-2
4. Grantham JJ (2008) Clinical practice. Autosomal dominant polycystic kidney disease. N Engl J Med 359(14):1477–1485. doi: 10.1056/NEJMcp0804458
5. Peters DJ, Sandkuijl LA (1992) Genetic heterogeneity of polycystic kidney disease in Europe. Contrib Nephrol 97:128–139
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