Kolexia
Mesnard Laurent
Néphrologie
Hôpital Tenon
Paris, France
264 Activités
843 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Maladies du rein Glomérulonéphrite Hypertension artérielle Atteinte rénale aigüe Défaillance rénale chronique Microangiopathies thrombotiques Hypertension artérielle maligne Insuffisance rénale Glomérulonéphrite à dépôts d'IgA

Industries

Sanofi
16 collaboration(s)
Dernière en 2023
Vifor
5 collaboration(s)
Dernière en 2023
TRAVERE THERAPEUTICS, INC.
4 collaboration(s)
Dernière en 2022
Chiesi
2 collaboration(s)
Dernière en 2022

Dernières activités

Assessment of epidemiology and outcomes of adult patients with kidney-limited thrombotic microangiopathies.
Kidney international   29 février 2024
Hot Spot of Complement Factor I Rare Variant p.Ile357Met in Patients With Hemolytic Uremic Syndrome.
American journal of kidney diseases : the official journal of the National Kidney Foundation   27 février 2024
IVAMA: Interrupters of VAscular daMAge in Malignant Hypertension: Role of Inflammasome, Angiogenic and Vasoactive System
Essai Clinique (Centre Hospitalier de Pau)   06 février 2024
TOTEM: Therapeutic Orientation Test in Thrombotic Microangiopathy
Essai Clinique (CHU Montpellier)   25 janvier 2024
Protective Role of the Podocyte IL-15 / STAT5 Pathway in Focal Segmental Glomerulosclerosis
Kidney international reports   10 janvier 2024
P392: Rapid complement mediated TMA diagnosis and early intervention in a renal intensive care unit using Nanopore technology
2024 ACMG Annual Clinical Genetics Meeting   01 janvier 2024
Mitochondrial nephropathy: MT-TL1 m.3243A>G mitochondrial DNA variant detected from whole exome sequencing can explain cases of adult unknown nephropathies
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference   01 janvier 2024
SeqOneRank+: a machine learning model to rank genetic variants based on phenotypes and ACMG criteria
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference   01 janvier 2024
Value of exome sequencing “first” for autosomal dominant polycystic kidney disease
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference   01 janvier 2024
Mining the pharmacogenetic treasure in exome sequencing data
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference   01 janvier 2024