Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Simona Borsa"'
Autor:
Elisa Dinoi, Alessandro Prete, Chiara Sardella, Laura Pierotti, Simone Della Valentina, Anna Dal Lago, Simona Borsari, Elena Pardi, Maria Adelaide Caligo, Angela Michelucci, Liborio Torregrossa, Piercarlo Rossi, Filomena Cetani
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
BackgroundBrown tumors are rare bone manifestations of primary hyperparathyroidism (PHPT) that may occur at different sites either as single or multiple lesions and they can easily be mistaken for malignant lesions. Neither bone site nor morphologica
Externí odkaz:
https://doaj.org/article/a52a770de3374413a70d323dd4e7019b
Autor:
Laura Pierotti, Elena Pardi, Elisa Dinoi, Paolo Piaggi, Simona Borsari, Simone Della Valentina, Chiara Sardella, Angela Michelucci, Maria Adelaide Caligo, Fausto Bogazzi, Claudio Marcocci, Filomena Cetani
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundMultiple Endocrine Neoplasia type 1 is a rare genetic syndrome mainly caused by mutations of MEN1 gene and characterized by a combination of several endocrine and non-endocrine manifestations. The objective of this study was to describe cut
Externí odkaz:
https://doaj.org/article/cddfb34863d94a4abb05977b30766764
Autor:
Graziella Bellone, Cristiana Rollino, Simona Borsa, Ivana Ferrero, Guido Martina, Anna Carbone, Katia Mareschi, Francesco Quarello, Giuseppe Piccoli, Giorgio Emanuelli, Lina Matera
Publikováno v:
Proceedings of the Society for Experimental Biology and Medicine. 223:367-371
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75b741a60e91449944d2d35ec417572f
https://doi.org/10.1111/j.1525-1373.2000.22352.x
https://doi.org/10.1111/j.1525-1373.2000.22352.x
Autor:
Maria Cristina Campopiano, Antonella Fogli, Angela Michelucci, Laura Mazoni, Antonella Longo, Simona Borsari, Elena Pardi, Elena Benelli, Chiara Sardella, Laura Pierotti, Elisa Dinoi, Claudio Marcocci, Filomena Cetani
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
The WNT1 gene is crucial for bone development and homeostasis. Homozygous mutations in WNT1 cause severe bone fragility known as osteogenesis imperfecta type XV. Moreover, heterozygous WNT1 mutations have been found in adults with early-onset osteopo
Externí odkaz:
https://doaj.org/article/64b0f84b0db84b1f96485bb926b48c52
Autor:
Annamaria Morotti, Filomena Cetani, Giulia Passoni, Simona Borsari, Elena Pardi, Vito Guarnieri, Chiara Verdelli, Giulia Stefania Tavanti, Luca Valenti, Cristiana Bianco, Stefano Ferrero, Sabrina Corbetta, Valentina Vaira
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Long non-coding RNAs (lncRNAs) are an important class of epigenetic regulators involved in both physiological processes and cancer development. Preliminary evidence suggested that lncRNAs could act as accurate prognostic and diagnostic biomarkers. Pa
Externí odkaz:
https://doaj.org/article/0b7d340b7350407c991c29d7d52c5bee
Publikováno v:
Journal of Immunological Methods. 185:141-143
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61ba40dc9a51eed5c1745b7ae93a5163
https://doi.org/10.1016/0022-1759(95)00171-6
https://doi.org/10.1016/0022-1759(95)00171-6
Autor:
Franco Bonello, Roberto Boero, Angelo Pignataro, Francesco Quarello, Giulietta Beltrame, M. Formica, Massimo Minelli, Simona Borsa, Cristiana Rollino
Publikováno v:
Renal failure. 22(5)
Cardiovascular disease accounts for almost half of the total mortality in patients with end stage renal disease (ESRD). It has recently been debated whether coronary revascularization has the same rate of risks and successes in this cohort of patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68f065190b4520e225c9ab85a588b943
https://pubmed.ncbi.nlm.nih.gov/11041292
https://pubmed.ncbi.nlm.nih.gov/11041292
Autor:
Marco Pozzato, Antonella Vallero, Francesco Quarello, Simona Borsa, Cristiana Rollino, Enrico Visetti, Angelo Pignataro
Publikováno v:
Artificial organs. 24(5)
Vecuronium is a curaric agent, largely used in anesthesia. Indications as to its employ in uremic patients appear to be debated because of partial renal elimination of the drug. A 52-year-old hemodialyzed woman required transplantectomy for rejection
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00c049b0a9aa6da67917fa75a0d8cafc
https://pubmed.ncbi.nlm.nih.gov/10848680
https://pubmed.ncbi.nlm.nih.gov/10848680
Autor:
Giorgio Emanuelli, Simona Borsa, Katia Mareschi, Lina Matera, Anna Carbone, Guido Martina, Francesco Quarello, Giuseppe Piccoli, Cristiana Rollino, Graziella Bellone, Ivana Ferrero
Publikováno v:
Scopus-Elsevier
The prolactin (PRL) receptor (R), a member of the cytokine hemopoietin receptor superfamily, has been shown to activate early differentiation steps along the erythroid pathway. In particular PRL, a product of bone marrow stroma, induces functional er
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adeeb251791215875e59f4bcb629131e
http://hdl.handle.net/2318/77946
http://hdl.handle.net/2318/77946
Autor:
Carlotta Giani, Teresa Ramone, Cristina Romei, Raffaele Ciampi, Alessia Tacito, Laura Valerio, Laura Agate, Clara Ugolini, Michele Marinò, Fulvio Basolo, Alessandro Franchi, Simona Borsari, Angela Michelucci, Cesare Selli, Gabriele Materazzi, Filomena Cetani, Rossella Elisei
Publikováno v:
Case Reports in Endocrinology, Vol 2020 (2020)
Background. Multiple endocrine neoplasia type 2 (MEN2) is a hereditary cancer syndrome caused by RET proto-oncogene mutation. Two different clinical variants of MEN2 are known (MEN2A and MEN2B): medullary thyroid carcinoma (MTC) almost always present
Externí odkaz:
https://doaj.org/article/735b841494db4930aef14e21dfdc9d20