Massimo Mannelli
Massimo Mannelli
Professore di Endocrinologia, Università di Firenze
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Consensus: guidelines for diagnosis and therapy of MEN type 1 and type 2
ML Brandi, RF Gagel, A Angeli, JP Bilezikian, P Beck-Peccoz, C Bordi, ...
The Journal of Clinical Endocrinology & Metabolism 86 (12), 5658-5671, 2001
JWM Lenders, G Eisenhofer, M Mannelli, K Pacak
The Lancet 366 (9486), 665-675, 2005
Biochemical diagnosis of pheochromocytoma: which test is best?
JWM Lenders, K Pacak, MCM Walther, WM Linehan, M Mannelli, ...
Jama 287 (11), 1427-1434, 2002
A prospective study of the prevalence of primary aldosteronism in 1,125 hypertensive patients
GP Rossi, G Bernini, C Caliumi, G Desideri, B Fabris, C Ferri, C Ganzaroli, ...
Journal of the American College of Cardiology 48 (11), 2293-2300, 2006
Pheochromocytoma: recommendations for clinical practice from the First International Symposium
K Pacak, G Eisenhofer, H Ahlman, SR Bornstein, AP Gimenez-Roqueplo, ...
Nature Reviews Endocrinology 3 (2), 92, 2007
Adjuvant mitotane treatment for adrenocortical carcinoma
M Terzolo, A Angeli, M Fassnacht, F Daffara, L Tauchmanova, PA Conton, ...
New England Journal of Medicine 356 (23), 2372-2380, 2007
Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma
I Comino-Méndez, FJ Gracia-Aznárez, F Schiavi, I Landa, ...
Nature genetics 43 (7), 663, 2011
An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective …
FH van Nederveen, J Gaal, J Favier, E Korpershoek, RA Oldenburg, ...
The lancet oncology 10 (8), 764-771, 2009
Renal damage in primary aldosteronism: results of the PAPY Study
GP Rossi, G Bernini, G Desideri, B Fabris, C Ferri, G Giacchetti, C Letizia, ...
Hypertension 48 (2), 232-238, 2006
The immune landscape of cancer
V Thorsson, DL Gibbs, SD Brown, D Wolf, DS Bortone, THO Yang, ...
Immunity 48 (4), 812-830. e14, 2018
Comprehensive characterization of cancer driver genes and mutations
MH Bailey, C Tokheim, E Porta-Pardo, S Sengupta, D Bertrand, ...
Cell 173 (2), 371-385. e18, 2018
Integrated genomic characterization of adrenocortical carcinoma
G Assié, E Letouzé, M Fassnacht, A Jouinot, W Luscap, O Barreau, ...
Nature genetics 46 (6), 607, 2014
The theory of constructed emotion: an active inference account of interoception and categorization
LF Barrett
Social cognitive and affective neuroscience 12 (1), 1-23, 2017
Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypes
G Eisenhofer, MM Walther, TT Huynh, ST Li, SR Bornstein, A Vortmeyer, ...
The Journal of Clinical Endocrinology & Metabolism 86 (5), 1999-2008, 2001
Oncogenic signaling pathways in the cancer genome atlas
F Sanchez-Vega, M Mina, J Armenia, WK Chatila, A Luna, KC La, ...
Cell 173 (2), 321-337. e10, 2018
Cell-of-origin patterns dominate the molecular classification of 10,000 tumors from 33 types of cancer
KA Hoadley, C Yau, T Hinoue, DM Wolf, AJ Lazar, E Drill, R Shen, ...
Cell 173 (2), 291-304. e6, 2018
Pheochromocytoma in Italy: a multicentric retrospective study
M Mannelli, L Ianni, A Cilotti, A Conti
European Journal of Endocrinology 141 (6), 619-624, 1999
Clinically guided genetic screening in a large cohort of Italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas
M Mannelli, M Castellano, F Schiavi, S Filetti, M Giacchè, L Mori, ...
The Journal of Clinical Endocrinology & Metabolism 94 (5), 1541-1547, 2009
MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma
N Burnichon, A Cascón, F Schiavi, NP Morales, I Comino-Méndez, ...
Clinical Cancer Research 18 (10), 2828-2837, 2012
Measurements of plasma methoxytyramine, normetanephrine, and metanephrine as discriminators of different hereditary forms of pheochromocytoma
G Eisenhofer, JWM Lenders, H Timmers, M Mannelli, SK Grebe, ...
Clinical chemistry 57 (3), 411-420, 2011
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Artículos 1–20