Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Enrica Mello"'
Autor:
Antonietta Vella, Elena De Carolis, Enrica Mello, David S. Perlin, Dominique Sanglard, Maurizio Sanguinetti, Brunella Posteraro
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
Abstract The echinocandins are relatively new antifungal drugs that represent, together with the older azoles, the recommended and/or preferred agents to treat candidaemia and other forms of invasive candidiasis in human patients. If “time is of th
Externí odkaz:
https://doaj.org/article/3374dd3f93e546dcbf3a5f20ef61d98d
Autor:
Elena De Carolis, Silvia Paoletti, Domenico Nagel, Antonietta Vella, Enrica Mello, Ivana Palucci, Giulia De Angelis, Tiziana D'Inzeo, Maurizio Sanguinetti, Brunella Posteraro, Teresa Spanu
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0185935 (2017)
Nowadays, the global spread of resistance to oxyimino-cephalosporins in Enterobacteriaceae implies the need for novel diagnostics that can rapidly target resistant organisms from these bacterial species.In this study, we developed and evaluated a Dir
Externí odkaz:
https://doaj.org/article/496e34eda74047fdb4b7196e6ebf3e9d
Autor:
Michele Miozzo, Martino Ongis, Francesca Peressotti, Vittorio Girotto, Eduardo Navarrete, Enrica Mello
Publikováno v:
Cognition. 199:104245
It has been shown that decisions and moral judgments differ when made using native languages compared to foreign languages. Cross-linguistic differences appeared in foreign languages that monolinguals typically acquired in school and used neither rou
Autor:
Daria Bottai, Brunella Posteraro, Antonella Lupetti, Cosmeri Rizzato, Enrica Mello, Maurizio Sanguinetti, Noemi Poma, Marina Zoppo, Arianna Tavanti
Publikováno v:
The Journal of antimicrobial chemotherapy. 73(7)
Background Candida orthopsilosis is a human fungal pathogen responsible for a wide spectrum of symptomatic infections. Evidence suggests that C. orthopsilosis is mainly susceptible to azoles, the most extensively used antifungals for treatment of the
Autor:
Elena De Carolis, Enrica Mello, Brunella Posteraro, Antonietta Vella, Riccardo Torelli, Maurizio Sanguinetti, Paul E. Verweij, Tiziana D'Inzeo
Publikováno v:
Antimicrobial Agents and Chemotherapy, 61, e00168-17-e00168-17
Antimicrobial Agents and Chemotherapy, 61, 6, pp. e00168-17-e00168-17
Antimicrobial Agents and Chemotherapy, 61, 6, pp. e00168-17-e00168-17
We tested 59 common and 27 uncommon Aspergillus species isolates for susceptibility to the mold-active azole antifungal agents itraconazole, voriconazole, and posaconazole using the Sensititre method. The overall essential agreement with the CLSI ref
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3a8cab99dd5fb29a350482f344a4e38
http://hdl.handle.net/10807/98185
http://hdl.handle.net/10807/98185
Publikováno v:
Clinica Chimica Acta. 424:85-89
Backgrounds Recently, we have considered two new findings in genetics of 21-hydroxylase deficiency with great interested: the existence of rare RCCX trimodular haplotypes, where the CYP21A2 like-gene downstream of the TNXA gene carries from one to si
Publikováno v:
Diagnostic Molecular Pathology. 22:48-51
More than 90% of congenital adrenal hyperplasia (CAH) cases are associated with mutations in the 21-hydroxylase gene (CYP21A2) in the HLA class III area on the short arm of chromosome 6p21.3. The major part of disease-causing mutations in CYP21A2 all
Autor:
Francesca Bugli, Maurizio Bossola, Brunella Posteraro, Gilda Pepe, Manuela Antocicco, Enrica Mello, Enrico Di Stasio, Carlo Vulpio, Maurizio Sanguinetti
Publikováno v:
Blood purification. 42(4)
Background: This study aims to evaluate, in patients on chronic hemodialysis (PHD), the levels of endotoxin through a chemiluminescent bioassay based on the oxidative burst reaction of activated neutrophils to complement coated LPS-IgM immune complex
Autor:
Silvana Penco, Cecilia Zuppi, Ettore Capoluongo, Enrica Mello, Maria Cristina Patrosso, Paola Concolino
Publikováno v:
Metabolism. 61:519-524
More than 90% of all cases of congenital adrenal hyperplasia (CAH) result from steroid 21-hydroxylase gene (CYP21A2) mutations. The CYP21A2 gene is located in the human leukocyte antigen (HLA) class III region on the short arm of chromosome 6p21.3, a
Publikováno v:
cclm. 48:1057-1062
Steroid 21-hydroxylase deficiency is present in more than 90% of patients with congenital adrenal hyperplasia, an inherited metabolic disorder of adrenal steroidogenesis. Impaired enzymatic activity leads to the accumulation of metabolic intermediate