Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Chiara Di Bella"'
Autor:
Emanuele David, Hektor Grazhdani, Lorenzo Aliotta, Livio Maria Gavazzi, Pietro Valerio Foti, Stefano Palmucci, Corrado Inì, Francesco Tiralongo, Davide Castiglione, Maurizio Renda, Patrizia Pacini, Chiara Di Bella, Carmen Solito, Silvia Gigli, Alessandro Fazio, Rita Bella, Antonio Basile, Vito Cantisani
Publikováno v:
Diagnostics, Vol 14, Iss 16, p 1708 (2024)
Atherosclerotic disease of the carotid arteries is a crucial risk factor in predicting the likelihood of future stroke events. In addition, emerging studies suggest that carotid stenosis may also be an indicator of plaque load on coronary arteries an
Externí odkaz:
https://doaj.org/article/68d3d0a6a9ea45a7973be68b61d4b598
Autor:
Emanuele David, Ombretta Martinelli, Patrizia Pacini, Marco Di Serafino, Pintong Huang, Vincenzo Dolcetti, Giovanni Del Gaudio, Richard G. Barr, Maurizio Renda, Giuseppe T. Lucarelli, Luca Di Marzo, Dirk A. Clevert, Carmen Solito, Chiara Di Bella, Vito Cantisani
Publikováno v:
Diagnostics, Vol 13, Iss 8, p 1478 (2023)
Atherosclerotic plaque in the carotid artery is the main cause of ischemic stroke, with a high incidence rate among people over 65 years. A timely and precise diagnosis can help to prevent the ischemic event and decide patient management, such as fol
Externí odkaz:
https://doaj.org/article/55e174d61f64469e8ed8d208e843f0f3
Autor:
Vincenzo Dolcetti, Eleonora Lori, Daniele Fresilli, Giovanni Del Gaudio, Chiara Di Bella, Patrizia Pacini, Vito D’Andrea, Fabrizio Maria Frattaroli, Giulia Giordana Vallone, Piero Liberatore, Daniele Pironi, Gian Luigi Canu, Pietro Giorgio Calò, Vito Cantisani, Salvatore Sorrenti
Publikováno v:
Cancers; Volume 15; Issue 9; Pages: 2644
Background: the aim of this study was to describe the ultrasound appearance of topical hemostatics after thyroidectomy. Methods: we enrolled 84 patients who were undergoing thyroid surgery and were treated with two types of topical hemostats, 49 with
Autor:
Antonio Tufano, Costantino Leonardo, Chiara Di Bella, Giuseppe Lucarelli, Vincenzo Dolcetti, Piervito Dipinto, Flavia Proietti, Rocco Simone Flammia, Umberto Anceschi, Sisto Perdonà, Giorgio Franco, Alessandro Sciarra, Giovanni Battista Di Pierro, Vito Cantisani
Background: We aimed to assess whether clear cell renal cell carcinoma (ccRCC) can be differentiated from renal oncocytoma (RO) on a contrast-enhanced ultrasound (CEUS). Methods: Between January 2021 and October 2022, we retrospectively queried and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aca908926c091325b204ce263f22ed01
https://hdl.handle.net/11573/1679139
https://hdl.handle.net/11573/1679139
Publikováno v:
Transfusion and Apheresis Science. 58:647-651
Thalassemias and sickle cell disease are a group of inherited blood disorders caused by alterations of the synthesis or of the structure of hemoglobin chains. It results in variable outcomes ranging from severe anemia to clinically asymptomatic indiv
Autor:
Fortunato Lombardo, Giuseppe d'Annunzio, Alessandro Salina, Emanuela Mazzon, Giuseppa Patti, Chiara Di Bella, Concetta Aloi, Luciana Rigoli, Giuseppina Salzano, Mohamad Maghnie, Rosario Caruso
We studied 45 patients with Wolfram syndrome 1 (WS1) to describe their clinical history and to search for possible genotype–phenotype correlations. Clinical criteria contributing to WS1 diagnosis were analyzed. The patients were classified into thr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be99acf7f9ffb292f21f9db1030e7555
http://hdl.handle.net/11567/966561
http://hdl.handle.net/11567/966561
Wolfram syndrome 1 (WS1) is a rare autosomal recessive neurodegenerative disease characterized by diabetes insipidus, diabetes mellitus, optic atrophy, deafness, and other abnormalities. WS1 usually results in death before the age of 50 years. The pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1571b3270bafe1d20231f3cc87a39833
http://hdl.handle.net/11570/3134763
http://hdl.handle.net/11570/3134763
Autor:
Rocco Bruno, Chiara Di Bella, Maria Amorini, Patrizia Longo, Carmelo Salpietro, Silvana Briuglia, Luciana Rigoli, Petronilla Daniela Romeo, Francesco Galletti
Publikováno v:
Annals of Human Genetics. 79:341-349
Mutations in the gene encoding the gap junction protein connexin 26 (GJB2) and connexin 30 (GJB6) have been shown to be a major contributor to prelingual, sensorineural, nonsyndromic deafness. The aim of this study was to characterize and establish t
Publikováno v:
Pediatric Research. 84:787-787
The original version of this Article erroneously cropped part of the abstract. The abstract has now been corrected to read 'Wolfram syndrome 1 (WS1) is a rare autosomal recessive neurodegenerative disease characterized by diabetes insipidus, diabetes