Kolexia
Edouard Thomas
Pédiatrie
Hôpital Paule de Viguier
Toulouse, France
138 Activités
3 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Syndrome de Noonan Syndrome de Marfan Syndrome de Loeys-Dietz Hypothyroïdie Anévrysme Anévrysme de l'aorte Rachitisme Ostéoporose Prédisposition génétique à une maladie

Industries

Novo Nordisk
3 collaboration(s)
Dernière en 2023
Ipsen
1 collaboration(s)
Dernière en 2021
Merck-Serono
1 collaboration(s)
Dernière en 2022
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{{person.topindus4.tot}} collaboration(s)
Dernière en {{person.topindus4.last}}

Dernières activités

BONeMOVE : an Adapted Physical Activity Program (APA) for Effort Rehabilitation of Children and Teenagers With Osteogenesis Imperfecta: an Interventional, Prospective, Regional, Bicentric Study.
Essai Clinique (CHU Toulouse)   27 février 2024
Exploring the genetic causes of isolated short stature. What has happened to idiopathic short stature?
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie   31 octobre 2023
Adult height improved over decades in patients with X-linked hypophosphatemia: a cohort study.
European journal of endocrinology   27 octobre 2023
Novel therapeutic perspectives in Noonan syndrome and RASopathies.
European journal of pediatrics   21 octobre 2023
Noonan: Constitution of a Biological Collection to Study the Pathophysiology in Noonan Syndrome and to Identify Predictive Factors of Disease Progression
Essai Clinique (CHU Toulouse)   25 mai 2023
RASTAT: Treatment With HMG-COA Reductase Inhibitor (Simvastatin) of Growth and Bone Abnormalities in Children With Noonan Syndrome: A Phase III Randomised, Double Blind, Placebo-controlled Therapeutic Trial
Essai Clinique (CHU Toulouse)   10 mai 2023
M&M's: Marfan&Moves (M&M's) : an Adapted Physical Activity Program (APA) for Effort Rehabilitation of Children and Teenagers With Marfan Syndrome: an Interventional, Prospective, Monocentric Study.
Essai Clinique (CHU Toulouse)   20 avril 2023
iPPSD, les pathologies de l’inactivation de la signalisation PTH/PTHrP (anciennement pseudohypoparathyroïdies et maladies associées)
HAS Publications   23 mars 2023
Clinical heterogeneity of NADSYN1-associated VCRL syndrome.
Clinical genetics   23 mars 2023
Obesity, Overweight, and Pituitary Stalk Interruption Syndrome in Children and Young Adults.
The Journal of clinical endocrinology and metabolism   26 janvier 2023