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Journal of Pediatric Endocrinology & Metabolism : JPEM|September 14, 2007
Identification of a novel mutation in the human growth hormone receptor gene (GHR) in a patient with Laron syndromeIsabelle Gennero, Thomas Edouard, Mona Rashad, et al.European Journal of Medical Genetics|November 26, 2009
Polyvalvular heart disease with joint hypermobility, characteristic facies, and particular skin abnormalities: new cases of "polyvalvular heart disease syndrome" or new association?Thomas Edouard, Catherine Prost-Squarcioni, Yves Dulac, et al.International Journal of Pediatric Endocrinology|July 14, 2012
Comparison of response to 2-years' growth hormone treatment in children with isolated growth hormone deficiency, born small for gestational age, idiopathic short stature, or multiple pituitary hormone deficiency: combined results from two large observational studiesPeter A Lee, Lars Sävendahl, Isabelle Oliver, et al.Biological Psychiatry|January 21, 2015
An Early Postnatal Oxytocin Treatment Prevents Social and Learning Deficits in Adult Mice Deficient for Magel2, a Gene Involved in Prader-Willi Syndrome and AutismHamid Meziane, Fabienne Schaller, Sylvian Bauer, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 7, 2015
Muscle and Bone Impairment in Children With Marfan Syndrome: Correlation With Age and FBN1 GenotypeElsa Haine, Jean-Pierre Salles, Philippe Khau Van Kien, et al.Orphanet Journal of Rare Diseases|July 9, 2021
Is ghrelin a biomarker of early-onset scoliosis in children with Prader-Willi syndrome?Dibia Liz Pacoricona Alfaro, Gwenaelle Diene, Graziella Pinto, et al.Bone|September 7, 2021
Low bone mass in Noonan syndrome children correlates with decreased muscle mass and low IGF-1 levelsMarine Delagrange, Vanessa Rousseau, Catie Cessans, et al.Nature Reviews. Disease Primers|April 22, 2022
Hypothalamic syndromeHermann L Müller, Maithé Tauber, Elizabeth A Lawson, et al.Plos One|November 13, 2015
Pituitary Stalk Interruption Syndrome from Infancy to Adulthood: Clinical, Hormonal, and Radiological Assessment According to the Initial PresentationCéline Bar, Charline Zadro, Gwenaelle Diene, et al.The Journal of Clinical Endocrinology and Metabolism|November 7, 2003
Adolescents with partial growth hormone (GH) deficiency develop alterations of body composition after GH discontinuation and require follow-upMaithé Tauber, Béatrice Jouret, Audrey Cartault, et al.Pageof 8