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Page 1
Clinical and Genetic Spectrum of Bartter Syndrome Type 3.
Seys E, Andrini O, Keck M, Mansour-Hendili L, Courand PY, Simian C, Deschenes G, Kwon T, Bertholet-Thomas A, Bobrie G, Borde JS, Bourdat-Michel G, Decramer S, Cailliez M, Krug P, Cozette P, Delbet JD, Dubourg L, Chaveau D, Fila M, Jourde-Chiche N, Knebelmann B, Lavocat MP, Lemoine S, Djeddi D, Llanas B, Louillet F, Merieau E, Mileva M, Mota-Vieira L, Mousson C, Nobili F, Novo R, Roussey-Kesler G, Vrillon I, Walsh SB, Teulon J, Blanchard A, Vargas-Poussou R. Seys E, et al. Among authors: vrillon i. J Am Soc Nephrol. 2017 Aug;28(8):2540-2552. doi: 10.1681/ASN.2016101057. Epub 2017 Apr 5. J Am Soc Nephrol. 2017. PMID: 28381550 Free PMC article.
Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome.
Legrand A, Treard C, Roncelin I, Dreux S, Bertholet-Thomas A, Broux F, Bruno D, Decramer S, Deschenes G, Djeddi D, Guigonis V, Jay N, Khalifeh T, Llanas B, Morin D, Morin G, Nobili F, Pietrement C, Ryckewaert A, Salomon R, Vrillon I, Blanchard A, Vargas-Poussou R. Legrand A, et al. Among authors: vrillon i. Clin J Am Soc Nephrol. 2018 Feb 7;13(2):242-250. doi: 10.2215/CJN.05670517. Epub 2017 Nov 16. Clin J Am Soc Nephrol. 2018. PMID: 29146702 Free PMC article.
Patient and transplant outcome in infants starting renal replacement therapy before 2 years of age.
Hogan J, Bacchetta J, Charbit M, Roussey G, Novo R, Tsimaratos M, Terzic J, Ulinski T, Garnier A, Merieau E, Harambat J, Vrillon I, Dunand O, Morin D, Berard E, Nobili F, Couchoud C, Macher MA; French Pediatric Nephrology Society. Hogan J, et al. Among authors: vrillon i. Nephrol Dial Transplant. 2018 Aug 1;33(8):1459-1465. doi: 10.1093/ndt/gfy040. Nephrol Dial Transplant. 2018. PMID: 29617835
Quality of life in adolescents with chronic kidney disease who initiate haemodialysis treatment.
Clavé S, Tsimaratos M, Boucekine M, Ranchin B, Salomon R, Dunand O, Garnier A, Lahoche A, Fila M, Roussey G, Broux F, Harambat J, Cloarec S, Menouer S, Deschenes G, Vrillon I, Auquier P, Berbis J. Clavé S, et al. Among authors: vrillon i. BMC Nephrol. 2019 May 14;20(1):163. doi: 10.1186/s12882-019-1365-3. BMC Nephrol. 2019. PMID: 31088395 Free PMC article.
School level of children carrying a HNF1B variant or a deletion.
Laliève F, Decramer S, Heidet L, Baudouin V, Lahoche A, Llanas B, Cochat P, Tenenbaum J, Lavocat MP, Eckart P, Broux F, Roussey G, Cloarec S, Vrillon I, Dunand O, Bessenay L, Tsimaratos M, Nobili F, Pietrement C, De Parscau L, Bonneville V, Rodier N, Saint-Martin C, Chassaing N, Michel-Calemard L, Moriniere V, Bellanné-Chantelot C, Bahans C, Guigonis V. Laliève F, et al. Among authors: vrillon i. Eur J Hum Genet. 2020 Jan;28(1):56-63. doi: 10.1038/s41431-019-0490-6. Epub 2019 Sep 3. Eur J Hum Genet. 2020. PMID: 31481685 Free PMC article.
Efficacy and safety of intravenous immunoglobulin with rituximab versus rituximab alone in childhood-onset steroid-dependent and frequently relapsing nephrotic syndrome: protocol for a multicentre randomised controlled trial.
Hogan J, Perez A, Sellier-Leclerc AL, Vrillon I, Broux F, Nobili F, Harambat J, Bessenay L, Audard V, Faudeux C, Morin D, Pietrement C, Tellier S, Djeddi D, Eckart P, Lahoche A, Roussey-Kesler G, Ulinski T, Boyer O, Plaisier E, Cloarec S, Jolivot A, Guigonis V, Guilmin-Crepon S, Baudouin V, Dossier C, Deschênes G. Hogan J, et al. Among authors: vrillon i. BMJ Open. 2020 Sep 23;10(9):e037306. doi: 10.1136/bmjopen-2020-037306. BMJ Open. 2020. PMID: 32967877 Free PMC article.
Renal Prognosis in Children With Tubulointerstitial Nephritis and Uveitis Syndrome.
Chevalier A, Duflos C, Clave S, Boyer O, Hogan J, Lahoche A, Decramer S, Broux F, Vrillon I, Allain-Launay E, Bacchetta J, Tanne C, Allard L, Cloarec S, Pietrement C, Bourdat-Michel G, Djeddi D, Dunand O, Faudeux C, Nobili F, Taque S, Ulinski T, Zaloszyc A, Morin D, Fila M. Chevalier A, et al. Among authors: vrillon i. Kidney Int Rep. 2021 Oct 7;6(12):3045-3053. doi: 10.1016/j.ekir.2021.09.017. eCollection 2021 Dec. Kidney Int Rep. 2021. PMID: 34901573 Free PMC article.
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