Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Luca Calvaruso"'
Autor:
Luca Calvaruso, Kevin Yau, Pedram Akbari, Fatemah Nasri, Saima Khowaja, Bill Wang, Amirreza Haghighi, Korosh Khalili, York Pei
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract Tolvaptan is the first disease-modifying drug proven to slow eGFR decline in high-risk patients with ADPKD. However, barriers from the patient perspective to its use in real-life settings have not been systemically examined in a large cohort
Externí odkaz:
https://doaj.org/article/54d5760c63ec449a81ab9e00f4b2a7de
Autor:
Gianmarco Lombardi, Pietro Manuel Ferraro, Luca Calvaruso, Alessandro Naticchia, Silvia D’Alonzo, Giovanni Gambaro
Publikováno v:
Kidney & Blood Pressure Research, Pp 1-11 (2019)
Background/Aims: Aim of our study was to describe the association between natremia (Na) fluctuation and hospital mortality in a general population admitted to a tertiary medical center. Methods: We performed a retrospective observational cohort study
Externí odkaz:
https://doaj.org/article/22488867ac8b429e9a750d840ce38289
Autor:
Luca Calvaruso, Alessandro Naticchia, Pietro Manuel Ferraro, Gisella Vischini, Stefano Costanzi
Publikováno v:
Case Reports in Nephrology, Vol 2019 (2019)
Background. Atypical hemolytic uremic syndrome (aHUS) is characterized by microangiopathic hemolytic anemia, thrombocytopenia, and renal failure. Mutations in CFI gene coding for complement regulation factors and in THBD gene coding for endothelial c
Externí odkaz:
https://doaj.org/article/e20ca4ba1b014a4f862ba6c2d1554b73
Autor:
Carmine Zoccali, Giovanni Tripepi, Alfonso Mele, Silvana Chicca, Elio Vitaliano, Marco Galliani, Luca Calvaruso, Antonio Paone, Maria Elena Tosti, Graziella D'Arrigo, Luca Di Lullo
Publikováno v:
Nephrology Dialysis Transplantation. 35
Background and Aims The natural history of ADPKD has been defined in numerous studies in various countries and in various genetic and environmental contexts but the problem has not yet been studied in sufficiently large studies in the Italian populat
Autor:
Silvana Chicca, Antonio Paone, L. Di Lullo, Francesco Iorio, Maria Elena Tosti, Elio Vitaliano, Marco Galliani, Luca Calvaruso
Publikováno v:
International Journal of Nephrology, Vol 2020 (2020)
International Journal of Nephrology
International Journal of Nephrology
The clinical manifestations of ADPKD are related to the growth of renal cysts. Renal volume has been recognised as the biomarker that is able to identify those patients at risk of complications (hypertension and haematuria) and at risk of progression
Autor:
Marco, Galliani, Silvana, Chicca, Elio, Vitaliano, Eleonora, Moscaritolo, Luca, Calvaruso, Francesco, Iorio, Antonio, Paone
Publikováno v:
Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia. 36(6)
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most frequent monogenic hereditary disease as well as the most studied inherited kidney disease. Two drugs have recently been authorized that can slow down the progression of the disease: To
Autor:
Pietro Manuel Ferraro, Alessandro Naticchia, Luca Calvaruso, Giovanni Gambaro, Silvia D'Alonzo, Gianmarco Lombardi
Publikováno v:
Kidney & Blood Pressure Research, Pp 1-11 (2019)
Background/Aims: Aim of our study was to describe the association between natremia (Na) fluctuation and hospital mortality in a general population admitted to a tertiary medical center. Methods: We performed a retrospective observational cohort study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47dcfb61be60dba5e55275c3b2495720
https://www.karger.com/Article/FullText/500916
https://www.karger.com/Article/FullText/500916
Autor:
Bruna Lo Sasso, Piera Dones, Chiara Bellia, Luisa Agnello, Giulia Bivona, Maria Di Gangi, Marcello Ciaccio, Concetta Scazzone, Luca Calvaruso
Publikováno v:
Clinical Biochemistry. 49:47-50
OBJECTIVES: Although the importance of serum Procalcitonin (PCT) levels at diagnosis is well established in adult Community-Acquired Pneumonia (CAP), its use remains controversial in pediatric CAP. The aim of our study is to investigate the role of P