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SON haploinsufficiency causes impaired pre-mRNA splicing of CAKUT genes and heterogeneous renal phenotypes.
Kim JH, Park EY, Chitayat D, Stachura DL, Schaper J, Lindstrom K, Jewett T, Wieczorek D, Draaisma JM, Sinnema M, Hoeberigs C, Hempel M, Bachman KK, Seeley AH, Stone JK, Kong HK, Vukadin L, Richard A, Shinde DN, McWalter K, Si YC, Douglas G, Lim ST, Vissers LELM, Lemaire M, Ahn EE. Kim JH, et al. Among authors: lemaire m. Kidney Int. 2019 Jun;95(6):1494-1504. doi: 10.1016/j.kint.2019.01.025. Epub 2019 Mar 15. Kidney Int. 2019. PMID: 31005274 Free PMC article.
A novel disease-causing mutation in AVPR2: Q96H.
Lemaire M, Chitayat D, Geary DF, Bichet DG, Licht C. Lemaire M, et al. NDT Plus. 2009 Feb;2(1):20-2. doi: 10.1093/ndtplus/sfn163. Epub 2008 Oct 31. NDT Plus. 2009. PMID: 25949277 Free PMC article.
Management of Severe Hyponatremia With a Custom Continuous Renal Replacement Therapy in an Infant With Newly Diagnosed Chronic Kidney Disease.
Gaudreault-Tremblay MM, Faqeehi H, Langlois V, Hébert D, Parra DA, Annich G, Harvey E, Lemaire M. Gaudreault-Tremblay MM, et al. Among authors: lemaire m. Kidney Int Rep. 2017 Jul 20;2(6):1254-1258. doi: 10.1016/j.ekir.2017.07.003. eCollection 2017 Nov. Kidney Int Rep. 2017. PMID: 29270536 Free PMC article. No abstract available.
Management of Canadian Pediatric Patients With Glomerular Diseases During the COVID-19 Pandemic: Recommendations From the Canadian Association of Pediatric Nephrologists COVID-19 Rapid Response Team.
Robinson C, Ruhl M, Kirpalani A, Alabbas A, Noone D, Teoh CW, Langlois V, Phan V, Lemaire M, Chanchlani R; authors of the CCRRT recommendations for adults with glomerulonephritis. Robinson C, et al. Among authors: lemaire m. Can J Kidney Health Dis. 2020 Nov 13;7:2054358120970713. doi: 10.1177/2054358120970713. eCollection 2020. Can J Kidney Health Dis. 2020. PMID: 33240518 Free PMC article.
528 results