Ferielle Louillet
Overview
Explore the profile of Ferielle Louillet including associated specialties, affiliations and a list of published articles.
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17
Citations
352
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0
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Recent Articles
1.
Buffin-Meyer B, Richard J, Guigonis V, Weber S, Konig J, Heidet L, et al.
Kidney Int Rep
. 2024 Aug;
9(8):2514-2526.
PMID: 39156164
Introduction: Hepatocyte nuclear factor 1-beta () gene variants or the chromosome 17q12 deletion (17q12del) represent the most common monogenic cause of developmental kidney disease. Although neurodevelopmental disorders have been associated...
2.
Meuleman M, Vieira-Martins P, El Sissy C, Audard V, Baudouin V, Bertrand D, et al.
Clin J Am Soc Nephrol
. 2023 Aug;
18(11):1435-1445.
PMID: 37615951
Background: C3 glomerulopathy and idiopathic immunoglobulin-mediated membranoproliferative GN (Ig-MPGN) are rare complement-mediated kidney diseases. Inherited forms of C3 glomerulopathy/Ig-MPGN are rarely described. Methods: Three hundred ninety-eight patients with C3 glomerulopathy...
3.
Nel I, Parmentier C, Dehoux L, Minier M, Duneton C, Charbit M, et al.
Transpl Int
. 2023 May;
36:11153.
PMID: 37252612
In this retrospective cohort study, we analyze the early humoral and cellular response in 64 adolescents KTx recipients, after two or three doses of mRNA vaccine BNT162b2 against different variants...
4.
Avramescu M, Isnard P, Temmam S, Chevalier A, Bastard P, Attia M, et al.
Kidney Int
. 2023 Mar;
103(6):1193-1198.
PMID: 36918081
No abstract available.
5.
Bedin M, Boyer O, Servais A, Li Y, Villoing-Gaude L, Tete M, et al.
J Clin Invest
. 2022 Jun;
132(11).
PMID: 35642643
No abstract available.
6.
Fakhouri F, Fila M, Hummel A, Ribes D, Sellier-Leclerc A, Ville S, et al.
Blood
. 2020 Dec;
137(18):2438-2449.
PMID: 33270832
The optimal duration of eculizumab treatment in patients with atypical hemolytic uremic syndrome (aHUS) remains poorly defined. We conducted a prospective national multicenter open-label study to assess eculizumab discontinuation in...
7.
Cointe A, Birgy A, Pascault A, Louillet F, Dufougeray A, Mariani-Kurkdjian P, et al.
Diagn Microbiol Infect Dis
. 2020 Sep;
98(4):115177.
PMID: 32966946
We report a hemolytic uremic syndrome (HUS) case due to Stx2f-producing E. coli illustrating the diagnostic difficulty of this Shiga-toxin subtype. Clinicians should be aware of limits of certain rapid...
8.
Chauvet S, Berthaud R, Devriese M, Mignotet M, Vieira Martins P, Robe-Rybkine T, et al.
J Am Soc Nephrol
. 2020 Feb;
31(4):829-840.
PMID: 32034108
Background: The pathophysiology of the leading cause of pediatric acute nephritis, acute postinfectious GN, including mechanisms of the pathognomonic transient complement activation, remains uncertain. It shares clinicopathologic features with C3...
9.
Bedin M, Boyer O, Servais A, Li Y, Villoing-Gaude L, Tete M, et al.
J Clin Invest
. 2019 Oct;
130(1):335-344.
PMID: 31613795
BACKGROUNDProteinuria is considered an unfavorable clinical condition that accelerates renal and cardiovascular disease. However, it is not clear whether all forms of proteinuria are damaging. Mutations in CUBN cause Imerslund-Gräsbeck...
10.
Lecoquierre F, Bonnevalle A, Chadie A, Gayet C, Dumant-Forest C, Renaux-Petel M, et al.
Am J Med Genet A
. 2019 Aug;
179(11):2257-2262.
PMID: 31390136
Introduction: SMG9 deficiency is an extremely rare autosomal recessive condition originally described in three patients from two families harboring homozygous truncating SMG9 variants in a context of severe syndromic developmental...