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Frontiers in Endocrinology|April 19, 2013
PROK2/PROKR2 Signaling and Kallmann SyndromeCatherine Dodé, Philippe RondardFASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|May 17, 2014
Biased signaling through G-protein-coupled PROKR2 receptors harboring missense mutationsOualid Sbai, Carine Monnier, Catherine Dodé, et al.Human Molecular Genetics|October 2, 2008
PROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activityCarine Monnier, Catherine Dodé, Ludovic Fabre, et al.Medecine Sciences : M/S|September 14, 2004
[Kallmann De Morsier syndrome: FGF-signaling insufficiency?]Catherine Dodé, Jean-Pierre HardelinJournal of Molecular Medicine (Berlin, Germany)|September 15, 2004
Kallmann syndrome: fibroblast growth factor signaling insufficiency?Catherine Dodé, Jean-Pierre HardelinEuropean Journal of Human Genetics : EJHG|November 6, 2008
Kallmann syndromeCatherine Dodé, Jean-Pierre HardelinCurrent Opinion in Pharmacology|December 23, 2014
Dynamics and modulation of metabotropic glutamate receptorsPhilippe Rondard, Jean-Philippe PinFrontiers of Hormone Research|April 15, 2010
Kallmann syndrome caused by mutations in the PROK2 and PROKR2 genes: pathophysiology and genotype-phenotype correlationsJulie Sarfati, Catherine Dodé, Jacques YoungLa Revue Du Praticien|March 28, 2002
[Hereditary intermittent fevers, other than familial Mediterranean fevers]Gilles Grateau, Laurence Cuisset, Catherine Dodé, et al.Journal of Nephrology|July 2, 2003
TNFRSF1A-associated periodic syndrome (TRAPS), Muckle-Wells syndrome (MWS) and renal amyloidosisCatherine Dodé, Laurence Cuisset, Marc Delpech, et al.Pageof 12