Zobrazeno 1 - 10
of 79
pro vyhledávání: '"Tonino, Ercolino"'
Autor:
Letizia Canu, Clotilde Sparano, Lara Naletto, Giuseppina De Filpo, Giulia Cantini, Elena Rapizzi, Serena Martinelli, Tonino Ercolino, Francesca Cioppi, Alessandro Fantoni, Lorenzo Zanatta, Alessandro Terreni, Massimo Mannelli, Michaela Luconi, Mario Maggi, Francesco Lotti
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2024)
PurposeAdrenocortical carcinoma (ACC) is a rare and aggressive tumor. ACC male patients under adjuvant mitotane therapy (AMT) frequently develop hypogonadism, however sexual function has never been assessed in this setting. The aim of this retrospect
Externí odkaz:
https://doaj.org/article/c80ae0ff8c364ee99c9961898ea05a70
Autor:
Giuseppina De Filpo, Gabriele Parenti, Clotilde Sparano, Giulia Rastrelli, Elena Rapizzi, Serena Martinelli, Francesca Amore, Benedetta Badii, Prosperi Paolo, Tonino Ercolino, Massimo Mannelli, Mario Maggi, Letizia Canu
Publikováno v:
World Journal of Surgical Oncology, Vol 21, Iss 1, Pp 1-11 (2023)
Abstract Background Pheochromocytoma (PHEO) and paraganglioma (PGL) are rare neuroendocrine tumors characterized by hemodynamic instability, caused by the paroxysmal release of catecholamines. Patients may develop cardiovascular complications in the
Externí odkaz:
https://doaj.org/article/184ef3415cb54945a846afb5c663e6de
Autor:
Giuseppina De Filpo, Gabriele Parenti, Clotilde Sparano, Giulia Rastrelli, Elena Rapizzi, Serena Martinelli, Francesca Amore, Benedetta Badii, Prosperi Paolo, Tonino Ercolino, Massimo Mannelli, Mario Maggi, Letizia Canu
Publikováno v:
World Journal of Surgical Oncology, Vol 21, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/48585d9e86aa4481b225a3f013905a4e
Autor:
Aldesia Provenzano, Massimiliano Chetta, Giuseppina De Filpo, Giulia Cantini, Andrea La Barbera, Gabriella Nesi, Raffaella Santi, Serena Martinelli, Elena Rapizzi, Michaela Luconi, Mario Maggi, Massimo Mannelli, Tonino Ercolino, Letizia Canu
Publikováno v:
Medicina, Vol 58, Iss 8, p 1113 (2022)
Background: Pheochromocytoma (Pheo) and paraganglioma (PGL) are rare tumors, mostly resulting from pathogenic variants of predisposing genes, with a genetic contribution that now stands at around 70%. Germline variants account for approximately 40%,
Externí odkaz:
https://doaj.org/article/1ea3b8f1701e4fdb8982deb96e3a7936
Autor:
Giulia Cantini, Laura Fei, Letizia Canu, Giuseppina De Filpo, Tonino Ercolino, Gabriella Nesi, Massimo Mannelli, Michaela Luconi
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Fascin-1 (FSCN1) is an actin-bundling protein associated with an invasive and aggressive phenotype of several solid carcinomas, as it is involved in cell cytoskeleton rearrangement and filopodia formation. Adrenocortical carcinoma (ACC) is a rare end
Externí odkaz:
https://doaj.org/article/42908f08651d4e14953819f4a99fc948
Autor:
Giuseppina De Filpo, Elisa Contini, Viola Serio, Andrea Valeri, Massimiliano Chetta, Daniele Guasti, Daniele Bani, Massimo Mannelli, Elena Rapizzi, Michaela Luconi, Mario Maggi, Tonino Ercolino, Letizia Canu
Publikováno v:
International Journal of Endocrinology, Vol 2020 (2020)
The genetic approach of pheochromocytomas and paragangliomas has changed in the last two decades. Nowadays, we know that more than 40% of patients have a germline mutation in one of the susceptibility genes identified to date. Our aim is to underline
Externí odkaz:
https://doaj.org/article/d8fc0e09e87348c19b751470b08d7b7a
Autor:
Letizia Canu, Silvia Pradella, Elena Rapizzi, Rossella Fucci, Andrea Valeri, Vittorio Briganti, Valentino Giachè, Gabriele Parenti, Tonino Ercolino, Massimo Mannelli
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 61, Iss 1, Pp 90-97 (2016)
SUMMARY Metastatic pheochromocytomas (PHEOs) and paragangliomas (sPGLs) are rare neural crest-derived tumors with a poor prognosis. About 50% of them are due to germ-line mutations of the SDHB gene. At present, there is no cure for these tumors. Thei
Externí odkaz:
https://doaj.org/article/704e8405433e4f37870d44a7317a6caa
Autor:
Mercedes Robledo, Anne-Paule Gimenez-Roqueplo, Graeme Eisenhofer, Giuseppe Opocher, Patricia L. M. Dahia, Massimo Mannelli, Karel Pacak, Felix Beuschlein, Miguel Urioste, Carli M.J. Tops, Henri J.L.M. Timmers, Elisa Taschin, Carlos Suarez, Alexander P.A. Stegmann, Frank Schillo, Macarena Ruiz-Ferrer, Giovanna Roncador, Nicole Reisch, Victoria Raymond, Elena Rapizzi, Nan Qin, Miguel Quesada-Charneco, Tamara Prodanov, Pierre-François Plouin, Peggy Pierre, Arnaud Murat, Luigi Mori, Anna Merlo, Arjen R. Mensenkamp, Rocío Letón, Jacques W.M. Lenders, Esther Korpershoek, Emiliano Honrado, Frederik J. Hes, Isabelle Guilhem, Álvaro Gómez-Graña, Encarna B. Gómez-García, Xavier Girerd, Tonino Ercolino, Ronald R. de Krijger, Mara Giacchè, Eleonora P.M. Corssmit, María-Dolores Chiara, Philippe Chanson, Maurizio Castellano, Salud Borrego, Sara Bobisse, Marinus J. Blok, Yves-Jean Bignon, Jérôme Bertherat, Sandra Bernaldo de Quirós, Marta Barontini, Laurence Amar, Aguirre A. de Cubas, Lucía Inglada-Pérez, Nasséra Abermil, Iñaki Comino-Méndez, Nicole Paes Morales, Francesca Schiavi, Alberto Cascón, Nelly Burnichon
Purpose: Pheochromocytomas (PCC) and paragangliomas (PGL) are genetically heterogeneous neural crest–derived neoplasms. Recently we identified germline mutations in a new tumor suppressor susceptibility gene, MAX (MYC-associated factor X), which pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e186187a379b455e8e5d962b4e1b154
https://doi.org/10.1158/1078-0432.c.6520958.v1
https://doi.org/10.1158/1078-0432.c.6520958.v1
Autor:
Michaela Luconi, Giulia Cantini, Rachel S. van Leeuwaarde, Rogina Roebaar, Laura Fei, Arianna Pia Propato, Raffaella Santi, Tonino Ercolino, Massimo Mannelli, Letizia Canu, Ronald R. de Krijger, Gabriella Nesi
Publikováno v:
Endocrine Pathology.
Adrenal cortical carcinoma (ACC) is an uncommon neoplasm with variable prognosis. Several histologic criteria have been identified as predictors of malignancy in adrenal cortical tumors. The Weiss score is the system most widely employed for diagnost
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00497d69605b27153845f76122359d15
https://doi.org/10.1007/s12022-023-09760-6
https://doi.org/10.1007/s12022-023-09760-6
Autor:
Giuseppina De Filpo, Antonio Cilotti, Luigi Rolli, Ugo Pastorino, Angelica Sonzogni, Silvia Pradella, Giulia Cantini, Tonino Ercolino, Gabriella Nesi, Massimo Mannelli, Mario Maggi, Letizia Canu
Publikováno v:
Medicina, Vol 56, Iss 11, p 561 (2020)
Background: Mutations in genes encoding one of the subunits of succinate dehydrogenase (SDH) are involved in pheochromocytoma (PHEO) and paraganglioma (PGL) development. Over the last few years, such mutations have also been associated with non-chrom
Externí odkaz:
https://doaj.org/article/2162c4b5521b466cba48166589516c5a