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The American Journal of Clinical Nutrition|June 9, 2007
Factors associated with overweight in preschool-age children in southwestern FranceBéatrice Jouret, Namanjeet Ahluwalia, Christelle Cristini, et al.Orphanet Journal of Rare Diseases|May 6, 2021
Effects of the COVID-19 pandemic and lockdown on the mental and physical health of adults with Prader-Willi syndromeHelena Mosbah, Muriel Coupaye, Flavien Jacques, et al.Endocrine Connections|March 3, 2023
Treatment burden, adherence, and quality of life in children with daily GH treatment in FranceRégis Coutant, Maithé Tauber, Béatrice Demaret, et al.American Journal of Medical Genetics. Part A|November 19, 2017
A model to characterize psychopathological features in adults with Prader-Willi syndromeDenise Thuilleaux, Virginie Laurier, Pierre Copet, et al.Endocrine Connections|November 8, 2022
The transition from pediatric to adult care in individuals with Prader-Willi syndromeChristine Poitou, Anthony Holland, Charlotte Höybye, et al.Molecular and Cellular Endocrinology|October 1, 2011
Two novel mutations in the thyroglobulin gene as cause of congenital hypothyroidism: identification a cryptic donor splice site in the exon 19Héctor M Targovnik, Thomas Edouard, Viviana Varela, et al.Genes|April 30, 2021
Growth Restriction and Genomic Imprinting-Overlapping Phenotypes Support the Concept of an Imprinting NetworkThomas Eggermann, Justin H Davies, Maithé Tauber, et al.Clinical Epigenetics|August 14, 2021
Patients with PWS and related syndromes display differentially methylated regions involved in neurodevelopmental and nutritional trajectoryJuliette Salles, Sanaa Eddiry, Emmanuelle Lacassagne, et al.Journal of Clinical Medicine|November 27, 2021
Diabetes Mellitus in Prader-Willi Syndrome: Natural History during the Transition from Childhood to Adulthood in a Cohort of 39 PatientsAlice Clerc, Muriel Coupaye, Héléna Mosbah, et al.The Journal of Clinical Endocrinology and Metabolism|September 24, 2016
Effect of Genotype and Previous GH Treatment on Adiposity in Adults With Prader-Willi SyndromeMuriel Coupaye, Maithé Tauber, Laurence Cuisset, et al.Pageof 8