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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.
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.
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.
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