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Page 1
Nomenclature for kidney function and disease: report of a Kidney Disease: Improving Global Outcomes (KDIGO) Consensus Conference.
Levey AS, Eckardt KU, Dorman NM, Christiansen SL, Hoorn EJ, Ingelfinger JR, Inker LA, Levin A, Mehrotra R, Palevsky PM, Perazella MA, Tong A, Allison SJ, Bockenhauer D, Briggs JP, Bromberg JS, Davenport A, Feldman HI, Fouque D, Gansevoort RT, Gill JS, Greene EL, Hemmelgarn BR, Kretzler M, Lambie M, Lane PH, Laycock J, Leventhal SE, Mittelman M, Morrissey P, Ostermann M, Rees L, Ronco P, Schaefer F, St Clair Russell J, Vinck C, Walsh SB, Weiner DE, Cheung M, Jadoul M, Winkelmayer WC. Levey AS, et al. Among authors: walsh sb. Kidney Int. 2020 Jun;97(6):1117-1129. doi: 10.1016/j.kint.2020.02.010. Epub 2020 Mar 9. Kidney Int. 2020. PMID: 32409237 Free article.
Pathogenesis of calcineurin inhibitor-induced hypertension.
Hoorn EJ, Walsh SB, McCormick JA, Zietse R, Unwin RJ, Ellison DH. Hoorn EJ, et al. Among authors: walsh sb. J Nephrol. 2012 May-Jun;25(3):269-75. doi: 10.5301/jn.5000174. J Nephrol. 2012. PMID: 22573529 Free PMC article. Review.
On the Origin of Urinary Renin: A Translational Approach.
Roksnoer LC, Heijnen BF, Nakano D, Peti-Peterdi J, Walsh SB, Garrelds IM, van Gool JM, Zietse R, Struijker-Boudier HA, Hoorn EJ, Danser AH. Roksnoer LC, et al. Among authors: walsh sb. Hypertension. 2016 May;67(5):927-33. doi: 10.1161/HYPERTENSIONAHA.115.07012. Epub 2016 Feb 29. Hypertension. 2016. PMID: 26928805 Free PMC article.
Genetic causes of hypomagnesemia, a clinical overview.
Viering DHHM, de Baaij JHF, Walsh SB, Kleta R, Bockenhauer D. Viering DHHM, et al. Among authors: walsh sb. Pediatr Nephrol. 2017 Jul;32(7):1123-1135. doi: 10.1007/s00467-016-3416-3. Epub 2016 May 27. Pediatr Nephrol. 2017. PMID: 27234911 Free PMC article. Review.
Genetic, pathophysiological, and clinical aspects of nephrocalcinosis.
Oliveira B, Kleta R, Bockenhauer D, Walsh SB. Oliveira B, et al. Among authors: walsh sb. Am J Physiol Renal Physiol. 2016 Dec 1;311(6):F1243-F1252. doi: 10.1152/ajprenal.00211.2016. Epub 2016 Sep 7. Am J Physiol Renal Physiol. 2016. PMID: 27605580 Free article. Review.
Fainting Fanconi syndrome clarified by proxy: a case report.
Walsh SB, Unwin R, Kleta R, Van't Hoff W, Bass P, Hussain K, Ellard S, Bockenhauer D. Walsh SB, et al. BMC Nephrol. 2017 Jul 11;18(1):230. doi: 10.1186/s12882-017-0649-8. BMC Nephrol. 2017. PMID: 28693455 Free PMC article.
Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies.
Ashton EJ, Legrand A, Benoit V, Roncelin I, Venisse A, Zennaro MC, Jeunemaitre X, Iancu D, Van't Hoff WG, Walsh SB, Godefroid N, Rotthier A, Del Favero J, Devuyst O, Schaefer F, Jenkins LA, Kleta R, Dahan K, Vargas-Poussou R, Bockenhauer D. Ashton EJ, et al. Among authors: walsh sb. Kidney Int. 2018 Apr;93(4):961-967. doi: 10.1016/j.kint.2017.10.016. Epub 2018 Feb 15. Kidney Int. 2018. PMID: 29398133 Free article.
Magnesium Balance in Chronic and End-Stage Kidney Disease.
Oliveira B, Cunningham J, Walsh SB. Oliveira B, et al. Among authors: walsh sb. Adv Chronic Kidney Dis. 2018 May;25(3):291-295. doi: 10.1053/j.ackd.2018.01.004. Adv Chronic Kidney Dis. 2018. PMID: 29793669 Review.
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