Regine Perrichot
Overview
Explore the profile of Regine Perrichot including associated specialties, affiliations and a list of published articles.
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5
Citations
403
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0
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Recent Articles
1.
Ducatez F, Mauhin W, Ottaviani J, Plichet T, Pilon C, Lidove O, et al.
J Clin Lab Anal
. 2024 Dec;
39(1):e25131.
PMID: 39727194
Background: Sphingolipidoses are rare inherited metabolic diseases belonging to lysosomal diseases. Early and accurate diagnosis is crucial for effective management and treatment. In this study, we aimed to develop a...
2.
Lefevre S, Audrezet M, Halimi J, Longuet H, Bridoux F, Ecotiere L, et al.
Nephrol Dial Transplant
. 2022 Feb;
37(11):2223-2233.
PMID: 35108395
Background: Autosomal dominant polycystic kidney disease (ADPKD) is associated with an increased risk for developing intracranial aneurysms (IAs). We aimed to evaluate the frequency of diagnosis of IAs in the...
3.
Gouin J, Dhalluin T, Perrichot R, Vigneau C, Michel A
Nephrol Ther
. 2020 Jul;
16(4):201-210.
PMID: 32653427
Introduction: ANCA-vasculitis are associated with high morbidity and mortality. Large use of cyclophosphamide as induction immunosuppressive therapy is limited by its side effects. All recent literature trends in decreasing cumulative...
4.
Cornec-Le Gall E, Audrezet M, Rousseau A, Hourmant M, Renaudineau E, Charasse C, et al.
J Am Soc Nephrol
. 2015 Jul;
27(3):942-51.
PMID: 26150605
The course of autosomal dominant polycystic kidney disease (ADPKD) varies among individuals, with some reaching ESRD before 40 years of age and others never requiring RRT. In this study, we...
5.
Cornec-Le Gall E, Audrezet M, Chen J, Hourmant M, Morin M, Perrichot R, et al.
J Am Soc Nephrol
. 2013 Feb;
24(6):1006-13.
PMID: 23431072
Autosomal dominant polycystic kidney disease (ADPKD) is heterogeneous with regard to genic and allelic heterogeneity, as well as phenotypic variability. The genotype-phenotype relationship in ADPKD is not completely understood. Here,...