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Journal of Pediatric Endocrinology & Metabolism : JPEM|November 18, 2016
Growth curves for congenital adrenal hyperplasia from a national retrospective cohortPatricia Bretones, Benjamin Riche, Emmanuel Pichot, et al.Journal of Pediatric Urology|April 1, 2014
Late prenatal dexamethasone and phenotype variations in 46,XX CAH: concerns about current protocols and benefits for surgical proceduresDaniela Gorduza, Véronique Tardy-Guidollet, Elsa Robert, et al.European Journal of Pediatrics|December 1, 2025
Growth hormone treatment outcomes in children with genetic isolated growth hormone deficiencyKarine Aouchiche, Sarah Castets, Isabelle Oliver Petit, et al.European Journal of Endocrinology|February 12, 2025
Phenotype and genotype of 23 patients with hypopituitarism and pathogenic GLI2 variantsKarine Aouchiche, Camille Charmensat, Pertuit Morgane, et al.Orphanet Journal of Rare Diseases|March 24, 2016
Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencingNadège Calmels, Géraldine Greff, Cathy Obringer, et al.Endocrine Connections|January 6, 2023
Changes in the clinical management of 5α-reductase type 2 and 17β-hydroxysteroid dehydrogenase type 3 deficiencies in FranceEstelle Bonnet, Mathias Winter, Delphine Mallet, et al.Orphanet Journal of Rare Diseases|July 12, 2022
Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol)Elodie Fiot, Bertille Alauze, Bruno Donadille, et al.Annales D'Endocrinologie|March 21, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditionsLaurence Faivre, Camille Level, Régis Coutant, et al.Annales D'Endocrinologie|May 8, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditionsLaurence Faivre, Camille Level, Régis Coutant, et al.Pageof 2