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Thyroid : Official Journal of the American Thyroid Association|June 18, 2010
New cases of isolated congenital central hypothyroidism due to homozygous thyrotropin beta gene mutations: a pitfall to neonatal screeningHelton E Ramos, Isabelle Labedan, Aurore Carré, et al.
The New England Journal of Medicine|April 25, 2008
Mutations in the iodotyrosine deiodinase gene and hypothyroidismJosé C Moreno, Willem Klootwijk, Hans van Toor, et al.
The Journal of Clinical Endocrinology and Metabolism|February 11, 2021
Long-Term Safety of Growth Hormone Treatment in Childhood: Two Large Observational Studies: NordiNet IOS and ANSWERLars Sävendahl, Michel Polak, Philippe Backeljauw, et al.
Best Practice & Research. Clinical Endocrinology & Metabolism|May 26, 2004
Fetal and neonatal thyroid function in relation to maternal Graves' diseaseMichel Polak, Isabelle Le Gac, Edith Vuillard, et al.
Human Genetics|August 25, 2007
Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesisAurore Carré, Mireille Castanet, Sylvia Sura-Trueba, et al.
Obesity Surgery|February 29, 2016
Postprandial GLP-1 Secretion After Bariatric Surgery in Three Cases of Severe Obesity Related to CraniopharyngiomasMarion Bretault, Suzanne Laroche, Jean-Marc Lacorte, et al.
European Journal of Endocrinology|August 18, 2020
First case of fetal goitrous hypothyroidism due to SLC5A5/NIS mutationsAthanasia Stoupa, Ghada Al Hage Chehade, Dulanjalee Kariyawasam, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2023
Early GH Treatment Is Effective and Well Tolerated in Children With Turner Syndrome: NordiNet® IOS and Answer ProgramPhilippe Backeljauw, Joanne C Blair, Jean-Marc Ferran, et al.
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