Výsledky vyhledávání - "Giuseppe Vancieri"

Akademický článek

Severe hypoglycemia in patients with known diabetes requiring emergency department care: A report from an Italian multicenter study

Autor: Alessandro Mantovani, Giorgio Grani, Laura Chioma, Giuseppe Vancieri, Ilaria Giordani, Roberta Rendina, Maria Elena Rinaldi, Aikaterini Andreadi, Carmela Coccaro, Chiara Boccardo, Costanza Fraenza, Giuliano Bertazzoni, Alfonso Bellia, Giacomo Zoppini, Giovanni Targher, Marco Giorgio Baroni, Davide Lauro, Massimino D'Armiento, Enzo Bonora

Publikováno v: Journal of Clinical & Translational Endocrinology, Vol 5, Iss C, Pp 46-52 (2016)

Aims: To describe the characteristics and associated risk factors of patients with established diabetes who required Emergency Department (ED) care for severe hypoglycemia. Methods: We performed an observational retrospective study to identify all ca

Externí odkaz: https://doaj.org/article/5d095f2200144156b13fcd318000d9c8

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Irsutismo: focus su patogenesi e diagnosi

Autor: Costanzo Moretti, Giuseppe Vancieri, Laura Guccione

Publikováno v: L'Endocrinologo. 22:544-552

L’irsutismo rappresenta un errore nella velocita proliferativa dei cheratinociti della matrice delle unita pilosebacee presenti in aree androgeno-sensibili della cute della donna. Esso e presente nel 5–15% delle donne prevalentemente adolescenti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::701227bde21016e522dad50eb74b852d
https://doi.org/10.1007/s40619-021-00987-1

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The Glu331del mutation in the CYP17A1 gene causes atypical congenital adrenal hyperplasia in a 46,XX female

Autor: Luca Federici, Elisa Menegatti, Francesco Brancati, Giulia Lanzolla, Silvia Lanciotti, Giuseppe Vancieri, Costanzo Moretti, Federica Sangiuolo

17α-Hydroxylase deficiency is an uncommon type of congenital adrenal hyperplasia (CAH) caused by mutations in the CYP17A1 gene encoding both 17α-hydroxylase and 17,20-lyase, essential for sex steroids production. Main clinical features include lack

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1edec2adb7300f39753e4efa5d2d7ef6
http://hdl.handle.net/11697/122112

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Virilizing Leydig-Sertoli cell ovarian tumor associated with endometrioid carcinoma of the endometrium in a postmenopausal patient: Case report and general considerations

Autor: Stefania Mariani, Salvatore Ulisse, Laura Guccione, Lucio Gnessi, Costanzo Moretti, Giuseppe Vancieri, Camillo Autore, Laura Chioma, Andrea Fabbri, Paola Di Giacinto, Elena Cicerone

Publikováno v: Clinical Medicine Insights. Case Reports
Clinical Medicine Insights: Case Reports, Vol 2012, Iss 5, Pp 149-153 (2012)
Clinical Medicine Insights: Case Reports, Vol 5 (2012)

Introduction Sertoli-Leydig cell tumors (SLCTs) are rare tumors mostly occurring in young women. Here we report an unusual case of a SLCT with simultaneous occurrence of endometrioid adenocarcinoma of the endometrium in a woman in menopause. Case Rep

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8677904823d827c31d8190b42c24eba6
http://hdl.handle.net/11573/483977

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