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European Journal of Endocrinology|June 27, 2014
Factors associated with vertebral fracture risk in patients with primary hyperparathyroidismCristina Eller-Vainicher, Claudia Battista, Vito Guarnieri, et al.
The Journal of Clinical Endocrinology and Metabolism|October 5, 2020
Mental Health in Patients With Adrenal Incidentalomas: Is There a Relation With Different Degrees of Cortisol Secretion?Valentina Morelli, Alberto Ghielmetti, Alice Caldiroli, et al.
European Journal of Endocrinology|January 17, 2022
Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disordersLucie Canaff, Vito Guarnieri, Yoojung Kim, et al.
Journal of Nephrology|May 17, 2014
Risk of nephrolithiasis in primary hyperparathyroidism is associated with two polymorphisms of the calcium-sensing receptor geneGiuseppe Vezzoli, Alfredo Scillitani, Sabrina Corbetta, et al.
The Journal of Clinical Endocrinology and Metabolism|January 14, 2016
JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid DefectsTiziana de Filippis, Federica Marelli, Gabriella Nebbia, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|April 14, 2026
Romosozumab super-responders in clinical practice: insights from a large Italian multicenter cohort of women with severe postmenopausal osteoporosisAlberto Ghielmetti, Giorgia Grassi, Silvia Carrara, et al.
Aging Clinical and Experimental Research|July 23, 2025
Bone status in patients with chronic hypoparathyroidism: results from the Italian HypoparaNET databaseFrancesca Marini, Francesca Giusti, Blandine Weiss, et al.
European Journal of Endocrinology|December 25, 2010
Polymorphisms at the regulatory regions of the CASR gene influence stone risk in primary hyperparathyroidismGiuseppe Vezzoli, Alfredo Scillitani, Sabrina Corbetta, et al.
European Journal of Endocrinology|June 26, 2019
Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin geneGiuseppa Patti, Saverio Scianguetta, Domenico Roberti, et al.
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