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Genetic studies of IgA nephropathy.
Maxwell PH, Wang Y. Maxwell PH, et al. Nephron Exp Nephrol. 2006;102(3-4):e76-80. doi: 10.1159/000089685. Epub 2005 Nov 11. Nephron Exp Nephrol. 2006. PMID: 16282702 Review.
C3 glomerulonephritis and CFHR5 nephropathy.
Gale DP, Maxwell PH. Gale DP, et al. Among authors: maxwell ph. Nephrol Dial Transplant. 2013 Feb;28(2):282-8. doi: 10.1093/ndt/gfs441. Epub 2012 Nov 2. Nephrol Dial Transplant. 2013. PMID: 23125424 Review.
Homozygous p.Ser267Phe in SLC10A1 is associated with a new type of hypercholanemia and implications for personalized medicine.
Liu R, Chen C, Xia X, Liao Q, Wang Q, Newcombe PJ, Xu S, Chen M, Ding Y, Li X, Liao Z, Li F, Du M, Huang H, Dong R, Deng W, Wang Y, Zeng B, Pan Q, Jiang D, Zeng H, Sham P, Cao Y, Maxwell PH, Gao ZL, Peng L, Wang Y. Liu R, et al. Among authors: maxwell ph. Sci Rep. 2017 Aug 23;7(1):9214. doi: 10.1038/s41598-017-07012-2. Sci Rep. 2017. PMID: 28835676 Free PMC article.
Renal replacement therapy for autosomal dominant polycystic kidney disease (ADPKD) in Europe: prevalence and survival--an analysis of data from the ERA-EDTA Registry.
Spithoven EM, Kramer A, Meijer E, Orskov B, Wanner C, Abad JM, Aresté N, de la Torre RA, Caskey F, Couchoud C, Finne P, Heaf J, Hoitsma A, de Meester J, Pascual J, Postorino M, Ravani P, Zurriaga O, Jager KJ, Gansevoort RT; ERA-EDTA Registry; EuroCYST Consortium; WGIKD. Spithoven EM, et al. Nephrol Dial Transplant. 2014 Sep;29 Suppl 4(Suppl 4):iv15-25. doi: 10.1093/ndt/gfu017. Nephrol Dial Transplant. 2014. PMID: 25165182 Free PMC article.
326 results