Multiple endocrine neoplasia syndrome type 1: institution, management, and data analysis of a nationwide multicenter patient database

Objective The aim of this study was to integrate European epidemiological data on patients with multiple endocrine neoplasia type 1 by creating an Italian registry of this syndrome, including clinical and genetic characteristics and therapeutic management. Methods Clinical, familial and genetic data...

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Veröffentlicht in:	Endocrine 2017-11, Vol.58 (2), p.349-359
Hauptverfasser:	Giusti, Francesca, Cianferotti, Luisella, Boaretto, Francesca, Cetani, Filomena, Cioppi, Federica, Colao, Annamaria, Davì, Maria Vittoria, Faggiano, Antongiulio, Fanciulli, Giuseppe, Ferolla, Piero, Ferone, Diego, Fossi, Caterina, Giudici, Francesco, Gronchi, Giorgio, Loli, Paola, Mantero, Franco, Marcocci, Claudio, Marini, Francesca, Masi, Laura, Opocher, Giuseppe, Beck-Peccoz, Paolo, Persani, Luca, Scillitani, Alfredo, Sciortino, Giovanna, Spada, Anna, Tomassetti, Paola, Tonelli, Francesco, Brandi, Maria Luisa
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Age Aged Aged, 80 and over Brain tumors Child Child, Preschool Data processing Diabetes Endocrinology Female Genetic Testing Humanities and Social Sciences Humans Hyperparathyroidism Insurance applications Internal Medicine Italy Life insurance Male Medicine Medicine & Public Health Middle Aged multidisciplinary Multiple endocrine neoplasia Multiple Endocrine Neoplasia Type 1 - diagnosis Multiple Endocrine Neoplasia Type 1 - genetics Mutation Neuroendocrine tumors Original Article Pedigree Pituitary Proto-Oncogene Proteins - genetics Registries Science Symptom Assessment Young Adult
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