Searchable abstracts of presentations at key conferences in endocrinology

ea0049gp204 | Thyroid 1 | ECE2017

24-month efficacy of a single radiofrequency ablation on autonomously functioning thyroid nodules

Bernardi Stella , Stacul Fulvio , Michelli Andrea , Calabro Veronica , Giudici Fabiola , Dobrinja Chiara , Fabris Bruno

Background: Radiofrequency ablation has been advocated as an alternative to radioiodine and/or surgery for the treatment of autonomously functioning benign thyroid nodules. However, only a few studies have measured radiofrequency ablation efficacy on autonomously functioning benign thyroid nodules. The aim of this work was to evaluate the 24-month efficacy of a single session of radiofrequency ablation (performed with the moving shot technique) on solitary autonomously functio...

ea0063p1002 | Environment, Society and Governance | ECE2019

Observational study on the cardio-metabolic effects of a night shift on internists

Bernardi Stella , Toffoli Barbara , Ferretti Tommaso , Francica Morena , Ghirigato Elena , Rovina Matteo , Calabro Veronica , Stenner Elisabetta , Giudici Fabiola , Fabris Bruno

Introduction: Shift work has been associated with increased cardiovascular morbidity and mortality. Several studies have demonstrated that shift work has an effect on cardiovascular and metabolic health. Most of these studies have compared different groups of shift workers to nonshift workers. By contrast, the present work aimed to evaluate the cardio-metabolic effects of night shifts on the same group of internists as they changed type of duty. In particular, we focused on bl...

ea0022p384 | Endocrine tumours &amp; neoplasia (<emphasis role="italic">Generously supported by Novartis</emphasis>) | ECE2010

Real-time PCR is useful to detect menin gene deletions

Zatelli Maria Chiara , Filieri Carlo , Tagliati Federico , Buratto Mattia , Calabro Veronica , Ambrosio Maria Rosaria , degli Uberti Ettore C

Familial pituitary adenoma is frequently associated with germinal mutations of several genes, including menin gene. MEN1 syndrome is an autosomic dominant disease, characterized by parathyroid adenomas, endocrine gastroenteropancreatic tumors, and pituitary adenomas, due to inactivating mutations of the MenI gene (11q13). MEN1 mutations are scattered within and around the menin open reading frame and are mainly represented by single nucleotide polymorphisms (SNPs), and ...