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Annales D'Endocrinologie|May 9, 2015
[Paternal GNAS mutations: Which phenotypes? What genetic counseling?]Marie-Laure Kottler
Medecine Sciences : M/S|September 12, 2022
[Pseudohypoparathyroidism and variants: A translational medicine success story]Marie-Laure Kottler
Annals of the New York Academy of Sciences|August 5, 2006
Aromatase gene expression and regulation in the female rat pituitaryGuillaume Galmiche, Sophie Corvaisier, Marie-Laure Kottler
The Journal of Pediatrics|June 18, 2013
Lightwood syndrome revisited with a novel mutation in CYP24 and vitamin D supplement recommendationsMireille Castanet, Eric Mallet, Marie-Laure Kottler
Endocrinology and Metabolism Clinics of North America|October 30, 2017
Genetic Diseases of Vitamin D Metabolizing EnzymesGlenville Jones, Marie Laure Kottler, Karl Peter Schlingmann
Peptides|October 25, 2008
KiSS-1 and GPR54 at the pituitary level: overview and recent insightsNicolas Richard, Sophie Corvaisier, Elise Camacho, et al.
Journal De La Societe De Biologie|May 19, 2004
[GnRH deficiency: new insights from genetics]Marie-Laure Kottler, Adèle Hamel, Elodie Malville, et al.
The Journal of Clinical Endocrinology and Metabolism|January 10, 2008
A maternal epimutation of GNAS leads to Albright osteodystrophy and parathyroid hormone resistanceVirginie Mariot, Stéphanie Maupetit-Méhouas, Christiane Sinding, et al.
The Journal of Steroid Biochemistry and Molecular Biology|January 14, 2009
The significance of the expression of ERRalpha as a potential biomarker in breast cancerKatarzyna Jarzabek, Mariusz Koda, Leszek Kozlowski, et al.
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