F Despert

A Comparative Phenotypic Study of Kallmann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes

Julie Sarfati, Anne Guiochon‐Mantel, Philippe Rondard et al. · The Journal of Clinical Endocrinology & Metabolism · 2009 · 145 citations

Demonstration by transfection studies that mutations in the adrenocorticotropin receptor gene are one cause of the hereditary syndrome of glucocorticoid deficiency.

Danielle Naville, Laure Barjhoux, Céline Jaillard et al. · The Journal of Clinical Endocrinology & Metabolism · 1996 · 90 citations · Full text

Genetics, Acth Receptor Gene, Glucocorticoid +18

Growth and Adult Height in GH-Treated Children with Nonacquired GH Deficiency and Idiopathic Short Stature: The Influence of Pituitary Magnetic Resonance Imaging Findings

R. Coutant, Stéphanie Rouleau, F Despert et al. · The Journal of Clinical Endocrinology & Metabolism · 2001 · 72 citations · Full text

Down Syndrome, Adult Height, Pituitary Magnetic Resonance +13

p.H62L, a Rare Mutation of the CYP21 Gene Identified in Two Forms of 21-Hydroxylase Deficiency

Rita Menassa, Véronique Tardy, F Despert et al. · The Journal of Clinical Endocrinology & Metabolism · 2008 · 37 citations

Partial hypoparathyroidism associated with mitochondrial trifunctional protein deficiency

François Labarthe, Jean François Benoist, M. Brivet et al. · European Journal of Pediatrics · 2006 · 36 citations

Mitochondrial Myopathy, Partial Hypoparathyroidism, Mitochondrial Function +3