Agnes Linglart, MD, PHD

INSERM U986, Service d'Endocrinologie Pédiatrique, Hôpital Bicêtre
Université Paris Sud – Centre de référence des maladies rares du métabolisme du calcium et du phosphore
Functional characterization of PRKAR1A mutants causing acrodysostosis with hormonal resistance
Anticalciuric Effect of Recombinant PTH in Patients with Activating Mutations of the Calcium-Sensing Receptor Causing Autosomal Dominant Hypocalcaemia-Hypercalciuria (ADHH)
FP10-2 Patients With Mutations In Phex Or FGF23 Share FGF23 Excess But Present Distinct BONE and Mineral Metabolism Features
FP25-6 Methylation and Transcripts Expression of GNAS Locus in Human iPSC and Their Differenciated Derivatives