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The Journal of Clinical Endocrinology and Metabolism|August 20, 2013
First birth achieved after in vitro maturation of oocytes from a woman endowed with multiple antral follicles unresponsive to follicle-stimulating hormoneMichaël Grynberg, Hellevi Peltoketo, Sophie Christin-Maître, et al.
The American Journal of Cardiology|March 10, 2009
Effects of testosterone on ventricular repolarization in hypogonadic menBeny Charbit, Sophie Christin-Maître, Jean-Louis Démolis, et al.
Fertility and Sterility|November 17, 2012
NR5A1 (SF-1) gene variants in a group of 26 young women with XX primary ovarian insufficiencyPascal Philibert, Françoise Paris, Besma Lakhal, et al.
European Journal of Nuclear Medicine and Molecular Imaging|November 16, 2006
Which thyroid cancer patients need periodic stimulation tests?Paolo Zanotti-Fregonara, Alexandre Khoury, Françoise Duron, et al.
Eating and Weight Disorders : EWD|April 3, 2020
Prevalence of lifetime eating disorders in infertile women seeking pregnancy with pulsatile gonadotropin-releasing hormone therapyIrema Barbosa-Magalhaes, Maurice Corcos, Julie Galey, et al.
European Journal of Public Health|September 3, 2015
Toward a multi-country monitoring system of reproductive health in the context of endocrine disrupting chemical exposureJoëlle Le Moal, Richard M Sharpe, Niels Jϕrgensen, et al.
Annales D'Endocrinologie|October 20, 2012
Hormonal contraception in women at risk of vascular and metabolic disorders: guidelines of the French Society of EndocrinologyPierre Gourdy, Anne Bachelot, Sophie Catteau-Jonard, et al.
European Journal of Endocrinology|April 9, 2008
Impact of total cumulative glucocorticoid dose on bone mineral density in patients with 21-hydroxylase deficiencyZeina Chakhtoura, Anne Bachelot, Dinane Samara-Boustani, et al.
American Journal of Medical Genetics. Part A|November 21, 2023
Stratification of the risk of ovarian dysfunction by studying the complexity of intermediate and premutation alleles of the FMR1 geneJuliette Quilichini, Sandrine Perol, Laurence Cuisset, et al.
Journal of Medical Genetics|August 20, 2025
Resolving structural variations missed by short-read sequencing uncovers their pathogenicityCaroline Schluth-Bolard, Laïla El Khattabi, Pierre-Antoine Rollat-Farnier, et al.
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