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Human Molecular Genetics|April 2, 2009
Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one caseAurore Carré, Gabor Szinnai, Mireille Castanet, et al.
Journal of the Endocrine Society|November 14, 2017
Study of the Factors Leading to Fetal and Neonatal Dysthyroidism in Children of Patients With Graves DiseaseMaïa Banigé, Candice Estellat, Valerie Biran, et al.
European Journal of Endocrinology|April 9, 2008
Impact of total cumulative glucocorticoid dose on bone mineral density in patients with 21-hydroxylase deficiencyZeina Chakhtoura, Anne Bachelot, Dinane Samara-Boustani, et al.
Head & Neck|July 6, 2026
Clinical, Radiologic and Cytologic Predictors of Malignancy in Pediatric Thyroid Nodules: Insights From a 26-Year Cohort StudyMaxime Gest-Laurent, Adrien Nguyen Quoc, Christine Lefevre, et al.
Frontiers in Endocrinology|October 26, 2023
Identifying patient-related predictors of permanent growth hormone deficiencyVeronica Mericq, German Iñiguez, Graziella Pinto, et al.
Nature Metabolism|November 26, 2024
Inceptor binds to and directs insulin towards lysosomal degradation in β cellsJohanna Siehler, Sara Bilekova, Prisca Chapouton, et al.
Hormone Research in Paediatrics|April 17, 2010
Low bone mineral density and high incidences of fractures and vitamin D deficiency in 52 pediatric cancer survivorsKalliopi Bilariki, Elli Anagnostou, Virginie Masse, et al.
The Journal of Clinical Endocrinology and Metabolism|January 13, 2006
Congenital hyperinsulinism: pancreatic [18F]fluoro-L-dihydroxyphenylalanine (DOPA) positron emission tomography and immunohistochemistry study of DOPA decarboxylase and insulin secretionPascale de Lonlay, Aurore Simon-Carre, Maria-João Ribeiro, et al.
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