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E2F1 germline copy number variations and melanoma susceptibility.
Rocca MS, Benna C, Mocellin S, Rossi CR, Msaki A, Di Nisio A, Opocher G, Foresta C. Rocca MS, et al. Among authors: opocher g. J Transl Med. 2019 May 29;17(1):181. doi: 10.1186/s12967-019-1933-0. J Transl Med. 2019. PMID: 31142321 Free PMC article.
Overexpression of L-Type Amino Acid Transporter 1 (LAT1) and 2 (LAT2): Novel Markers of Neuroendocrine Tumors.
Barollo S, Bertazza L, Watutantrige-Fernando S, Censi S, Cavedon E, Galuppini F, Pennelli G, Fassina A, Citton M, Rubin B, Pezzani R, Benna C, Opocher G, Iacobone M, Mian C. Barollo S, et al. Among authors: opocher g. PLoS One. 2016 May 25;11(5):e0156044. doi: 10.1371/journal.pone.0156044. eCollection 2016. PLoS One. 2016. PMID: 27224648 Free PMC article. Clinical Trial.
Rare diseases in clinical endocrinology: a taxonomic classification system.
Marcucci G, Cianferotti L, Beck-Peccoz P, Capezzone M, Cetani F, Colao A, Davì MV, degli Uberti E, Del Prato S, Elisei R, Faggiano A, Ferone D, Foresta C, Fugazzola L, Ghigo E, Giacchetti G, Giorgino F, Lenzi A, Malandrino P, Mannelli M, Marcocci C, Masi L, Pacini F, Opocher G, Radicioni A, Tonacchera M, Vigneri R, Zatelli MC, Brandi ML. Marcucci G, et al. Among authors: opocher g. J Endocrinol Invest. 2015 Feb;38(2):193-259. doi: 10.1007/s40618-014-0202-6. Epub 2014 Nov 7. J Endocrinol Invest. 2015. PMID: 25376364
Multiple endocrine neoplasia type 1: analysis of germline MEN1 mutations in the Italian multicenter MEN1 patient database.
Marini F, Giusti F, Fossi C, Cioppi F, Cianferotti L, Masi L, Boaretto F, Zovato S, Cetani F, Colao A, Davì MV, Faggiano A, Fanciulli G, Ferolla P, Ferone D, Loli P, Mantero F, Marcocci C, Opocher G, Beck-Peccoz P, Persani L, Scillitani A, Guizzardi F, Spada A, Tomassetti P, Tonelli F, Brandi ML. Marini F, et al. Among authors: opocher g. Endocrine. 2018 Oct;62(1):215-233. doi: 10.1007/s12020-018-1566-8. Epub 2018 Mar 1. Endocrine. 2018. PMID: 29497973
Gain-of-function mutations in DNMT3A in patients with paraganglioma.
Remacha L, Currás-Freixes M, Torres-Ruiz R, Schiavi F, Torres-Pérez R, Calsina B, Letón R, Comino-Méndez I, Roldán-Romero JM, Montero-Conde C, Santos M, Pérez LI, Pita G, Alonso MR, Honrado E, Pedrinaci S, Crespo-Facorro B, Percesepe A, Falcioni M, Rodríguez-Perales S, Korpershoek E, Ramón-Maiques S, Opocher G, Rodríguez-Antona C, Robledo M, Cascón A. Remacha L, et al. Among authors: opocher g. Genet Med. 2018 Dec;20(12):1644-1651. doi: 10.1038/s41436-018-0003-y. Epub 2018 May 8. Genet Med. 2018. PMID: 29740169 Free article.
190 results