Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Irene, Cirella"'
Autor:
Federico Nalesso, Federica L. Stefanelli, Valentina Di Vico, Leda Cattarin, Irene Cirella, Giuseppe Scaparrotta, Francesco Garzotto, Lorenzo A. Calò
Publikováno v:
Biomedicines, Vol 10, Iss 8, p 2017 (2022)
Critical clinical forms of COVID-19 infection often include Acute Kidney Injury (AKI), requiring kidney replacement therapy (KRT) in up to 20% of patients, further worsening the outcome of the disease. No specific medical therapies are available for
Externí odkaz:
https://doaj.org/article/f2851d59c5554984b77c8c7d6443be41
Autor:
Federico Nalesso, Matteo Rigato, Irene Cirella, Maria Paola Protti, Ruggero Zanella, Bartolomeo Rossi, Maria Caterina Putti, Francesca K. Martino, Lorenzo A. Calò
Publikováno v:
Journal of Clinical Medicine; Volume 11; Issue 22; Pages: 6752
Beta-thalassemia syndromes are the most common inherited monogenic disorders worldwide. The most common pathophysiologic and clinical renal disease manifestations of in β-TM patients is the tubular dysfunctions related to iron overload, chronic anem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b6fc64d748b60e6b5e9f2f89c75f939
Autor:
Irene, Cirella, Valentina, di Vico, Matteo, Rigato, Beatrice, Bugnotto, Paola, Baldini Anastasio, Daniela, Campo, Gianni, Carraro, Lorenzo A, Calò
Publikováno v:
Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia. 39(3)
Autosomal dominant polycystic kidney disease (ADPKD) is responsible of the 10% of the dialysis patients. Tolvaptan is a consolidate option for treatment of ADPKD patients; it slows renal deterioration rate and cysts' growth, although its acquaretic e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::85cc04363bffe95c0a4a2e4f0812e3c8
https://pubmed.ncbi.nlm.nih.gov/35819042
https://pubmed.ncbi.nlm.nih.gov/35819042
Publikováno v:
Clinical Nephrology. 96:60-62
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad5673c99ad9d71500aabe5f5b97f723
https://doi.org/10.5414/cn110444
https://doi.org/10.5414/cn110444