Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Francesco Cocchiara"'
Autor:
Cristian Petolicchio, Sara Brasili, Stefano Gay, Francesco Cocchiara, Irene Campi, Luca Persani, Lara Vera, Diego Ferone, Federico Gatto
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-6 (2024)
The resistance to thyroid hormone syndrome (RTHβ) occurs uncommonly and requires a high level of clinical suspicion and specific investigations to reach a precise diagnosis and to avoid unnecessary and potentially harmful therapies. We report a case
Externí odkaz:
https://doaj.org/article/7244d6628d124ba787df8d6f9712d5f9
Autor:
Diletta Favero, Christoph Oing, Christoph Seidel, Pasquale Rescigno, Fabio Catalano, Malvina Cremante, Sara Elena Rebuzzi, Federico Gatto, Giovanni Rosti, Diego Ferone, Giuseppe Fornarini, Francesco Cocchiara
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
BackgroundHuman chorionic gonadotropin (hCG)–induced hyperthyroidism is a rare paraneoplastic syndrome observed in non-seminomatous testicular germ cell tumors, due to a cross-reaction between the β-subunit of hCG with the thyroid-stimulating horm
Externí odkaz:
https://doaj.org/article/5259fec7c6e74c8583c353c4dd9cb4da
Autor:
Marta Franco, Keyvan Khorrami Chokami, Manuela Albertelli, Claudia Teti, Francesco Cocchiara, Federico Gatto, Carlo Trombetta, Diego Ferone, Mara Boschetti
Publikováno v:
BMC Endocrine Disorders, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Background The vanishing testis syndrome (VTS), is a 46, XY disorder of sex development (46, XY DSD) and is characterized by the absence of testis in a 46, XY subject with male genitalia, gonadal dysgenesis and consequent hypergonadotropic h
Externí odkaz:
https://doaj.org/article/8bd36ed7630b40b2a848c33a38611be9
Autor:
Federica Nista, Giuliana Corica, Lara Castelletti, Keyvan Khorrami, Claudia Campana, Francesco Cocchiara, Gabriele Zoppoli, Alessandro Prior, Diego Criminelli Rossi, Gianluigi Zona, Diego Ferone, Federico Gatto
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
BackgroundFirst-generation somatostatin receptor ligands (fg-SRLs) represent the first-line medical treatment for acromegaly, recommended in patients with persistent disease after neurosurgery, or when surgical approach is not feasible. Despite the l
Externí odkaz:
https://doaj.org/article/39b084047c174c93808fb5c1145628b5
Autor:
Francesco Cocchiara, Keyvan Khorrami, Diego Ferone, Giuliana Corica, Marta Franco, Claudia Campana, Federico Gatto, Giulia Graziani, Mara Boschetti, Federica Nista
Publikováno v:
Expert Opinion on Emerging Drugs. 25:409-417
Acromegaly is a disease characterized by elevated growth hormone (GH) and insulin-like growth factor 1 (IGF-1) levels. Surgery is the only curative treatment, while medical therapies are administered life-long. To date, almost 30% of patients treated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff3734fa6f7585593687112fdf842e56
https://doi.org/10.1080/14728214.2020.1819983
https://doi.org/10.1080/14728214.2020.1819983
Autor:
Federico Gatto, Diego Criminelli, Claudia Campana, Francesco Cocchiara, Federica Nista, Mara Boschetti, Giuliana Corica, Diego Ferone, Gianluigi Zona, Marco Ceraudo
Publikováno v:
Therapeutics and Clinical Risk Management. 16:379-391
Acromegaly is a rare and severe disease caused by an increased and autonomous secretion of growth hormone (GH), thus resulting in high circulating levels of insulin-like growth factor 1 (IGF-1). Comorbidities and mortality rate are closely related to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eee53daf28a0aef8ffe2d0db04a47b28
https://doi.org/10.2147/tcrm.s183360
https://doi.org/10.2147/tcrm.s183360
Autor:
Norbert, Maggi, Ariam, Boaglio, Carmelina, Ruggiero, Roberto, Fancellu, Francesco, Cocchiara, Domenico, Coviello, Deborah, Capanna, Mauro, Giacomini
Publikováno v:
Studies in health technology and informatics. 287
Undiagnosed rare diseases include diseases with a well-characterised phenotype, diseases with unknown molecular causes or due to non-genetic factors, and pathological condition that cannot be named. Several initiatives have been launched for healthca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6931f0267c9d9244ab5a3fc00bcbd15f
https://pubmed.ncbi.nlm.nih.gov/34795093
https://pubmed.ncbi.nlm.nih.gov/34795093
Autor:
Diego Criminelli Rossi, Marco Ceraudo, Federica Nista, Gianluigi Zona, Francesco Cocchiara, Diego Ferone, Giuliana Corica, Claudia Campana, Federico Gatto, Angelo Milioto
Publikováno v:
Pituitary. 25(2)
PURPOSE Acromegaly is a severe chronic endocrine disease. Achieving biochemical control often needs a multimodal treatment approach, including prolonged medical treatment. Aim of the study is to evaluate the burden of treatment direct costs with resp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e4782f54bec792dbb6e32e03928ead8
https://pubmed.ncbi.nlm.nih.gov/34757473
https://pubmed.ncbi.nlm.nih.gov/34757473
Autor:
Claudia Campana, Diego Ferone, Federico Gatto, Marica Arvigo, Francesco Cocchiara, Jessica Amarù, Federica Nista, Giuliana Corica, Gianluigi Zona, Diego Criminelli Rossi
Context Discordant growth hormone (GH) and insulin-like growth factor-1 (IGF-1) values are frequent in acromegaly. Objective To evaluate the impact of different GH cutoffs on discordance rate. To investigate whether the mean of consecutive GH measure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22d7f80f35ed23a7057ee2d77ddee6a5
http://hdl.handle.net/11567/1044725
http://hdl.handle.net/11567/1044725
Autor:
Roberto Fancellu, Domenico Coviello, Mauro Giacomini, Ariam Boaglio, Norbert Maggi, Carmelina Ruggiero, Deborah Capanna, Francesco Cocchiara
Undiagnosed rare diseases include diseases with a well-characterised phenotype, diseases with unknown molecular causes or due to non-genetic factors, and pathological condition that cannot be named. Several initiatives have been launched for healthca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f01f4c15a5d33493c5d0d7db9e1e91c8
https://hdl.handle.net/11567/1083024
https://hdl.handle.net/11567/1083024