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Sabrina Corbetta

Showing results (81-90 of 99) with videos related to

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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|July 2, 2010
Influence of the d3GH receptor polymorphism on the metabolic and biochemical phenotype of GH-deficient adults at baseline and during short- and long-term recombinant human GH replacement therapyClaudia Giavoli, Emanuele Ferrante, Eriselda Profka, et al.
Endocrine|November 19, 2011
A rare S33C mutation of CTNNB1 encoding β-catenin in a parathyroid adenoma found in an Italian primary hyperparathyroid cohortVito Guarnieri, Filomena Baorda, Claudia Battista, 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.
The Journal of Clinical Endocrinology and Metabolism|October 4, 2014
Increased prevalence of the GCM2 polymorphism, Y282D, in primary hyperparathyroidism: analysis of three Italian cohortsLeonardo D'Agruma, Michela Coco, Vito Guarnieri, et al.
Pageof 10

Showing results (81-90 of 99) with videos related to

Sort By:
Pageof 10
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|July 2, 2010
Influence of the d3GH receptor polymorphism on the metabolic and biochemical phenotype of GH-deficient adults at baseline and during short- and long-term recombinant human GH replacement therapyClaudia Giavoli, Emanuele Ferrante, Eriselda Profka, et al.
Endocrine|November 19, 2011
A rare S33C mutation of CTNNB1 encoding β-catenin in a parathyroid adenoma found in an Italian primary hyperparathyroid cohortVito Guarnieri, Filomena Baorda, Claudia Battista, 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.
The Journal of Clinical Endocrinology and Metabolism|October 4, 2014
Increased prevalence of the GCM2 polymorphism, Y282D, in primary hyperparathyroidism: analysis of three Italian cohortsLeonardo D'Agruma, Michela Coco, Vito Guarnieri, et al.
Pageof 10