Kolexia
Netchine Irene
Pédiatrie
Hôpital Armand Trousseau
Paris, France
146 Activités
7 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Syndrome de Silver-Russell Syndrome de Beckwith-Wiedemann Imprinting Disorders Retard de croissance intra-utérin Troubles de la croissance Disomie uniparentale Puberté précoce Maladies rares Prédisposition génétique à une maladie

Industries

Novartis
3 collaboration(s)
Dernière en 2022
Sandoz
3 collaboration(s)
Dernière en 2023
Merck-Serono
1 collaboration(s)
Dernière en 2020
Novo Nordisk
1 collaboration(s)
Dernière en 2023

Dernières activités

Pubertal origin of growth retardation in inborn errors of protein metabolism: A longitudinal cohort study.
Molecular genetics and metabolism   01 janvier 2024
The experience of diagnosis announcement in rare endocrine diseases: A survey of the French FIRENDO network.
Annales d'endocrinologie   10 novembre 2023
Electronic reporting of rare endocrine conditions within a clinical network - results from the EuRRECa project.
Endocrine connections   01 octobre 2023
IDMet: National Cohort on Imprinting Disorders and Their Metabolic Consequences
Essai Clinique (Institut National de la Santé Et de la Recherche Médicale, France)   06 juillet 2023
Executive functioning in adolescents and adults with Silver-Russell syndrome.
PloS one   20 janvier 2023
Maintenance of methylation profile in imprinting control regions in human induced pluripotent stem cells.
Clinical epigenetics   28 décembre 2022
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders.
Clinical epigenetics   07 novembre 2022
Comprehensive genetic testing approaches as the basis for personalized management of growth disturbances: current status and perspectives.
Endocrine connections   10 octobre 2022
Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol).
Orphanet journal of rare diseases   12 juillet 2022
Analysis of a pitfall in congenital adrenal hyperplasia newborn screening: evidence of maternal use of corticoids detected on dried blood spot.
Endocrine connections   15 juin 2022