Zobrazeno 1 - 10
of 74
pro vyhledávání: '"Chiara, Di Resta"'
Autor:
Chiara Di Resta, Valeria D'Argenio
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Externí odkaz:
https://doaj.org/article/7879e8a6351e4ac7b839c65f54512b6d
Autor:
Rossella Tomaiuolo, Chiara Di Resta, Marco Viganò, Giuseppe Banfi, Cristina Russo, Giulia Linardos, Stefania Ranno, Carlo Federico Perno, Francesco Giuffrida
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-7 (2022)
Abstract Ageing is associated with a progressive decline and remodelling of the immune system. Also, the efficacy of COVID-19 vaccines has been observed to depend on subjects’ age. The post-vaccination data about patients aged > 90 years old is sca
Externí odkaz:
https://doaj.org/article/ff6e70b7bdc74f6086a7effdd33f865f
Autor:
Eleonora Sabetta, Maddalena Noviello, Clara Sciorati, Marco Viganò, Rebecca De Lorenzo, Valeria Beretta, Veronica Valtolina, Chiara Di Resta, Giuseppe Banfi, Davide Ferrari, Massimo Locatelli, Fabio Ciceri, Chiara Bonini, Patrizia Rovere-Querini, Rossella Tomaiuolo
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
IntroductionSARS-CoV-2 mRNA vaccinations elicit both virus-specific humoral and T-cell responses, but a complex interplay of different influencing factors, such as natural immunity, gender, and age, guarantees host protection. The present study aims
Externí odkaz:
https://doaj.org/article/53f0f1f4c7b648dcaa01143b315a5448
Publikováno v:
Biomolecules, Vol 13, Iss 10, p 1441 (2023)
Recent technical breakthroughs in genotyping and bioinformatics techniques have greatly facilitated the translation of genomics into clinical care [...]
Externí odkaz:
https://doaj.org/article/d4f08f7feaf24414b8aa21ae01c363ea
Autor:
Federica Banfi, Alicia Rubio, Mattia Zaghi, Luca Massimino, Giulia Fagnocchi, Edoardo Bellini, Mirko Luoni, Cinzia Cancellieri, Anna Bagliani, Chiara Di Resta, Camilla Maffezzini, Angelo Ianielli, Maurizio Ferrari, Rocco Piazza, Luca Mologni, Vania Broccoli, Alessandro Sessa
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-21 (2021)
Schinzel-Giedion syndrome (SGS) is a fatal developmental syndrome characterized by severe intellectual and physical deficits due, at least in part, to early neurodegeneration. Here the authors introduce a human SGS model that displays disease-relevan
Externí odkaz:
https://doaj.org/article/9f82d3e4675e4ed291494e6ac2e0dfe7
Autor:
Nicolò Salvarani, Giovanni Peretto, Crasto Silvia, Andrea Villatore, Cecilia Thairi, Anna Santoni, Camilla Galli, Paola Carrera, Simone Sala, Sara Benedetti, Elisa Di Pasquale, Chiara Di Resta
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 11, p 9548 (2023)
Brugada syndrome (BrS) is an inherited autosomal dominant cardiac channelopathy. Pathogenic rare mutations in the SCN5A gene, encoding the alpha-subunit of the voltage-dependent cardiac Na+ channel protein (Nav1.5), are identified in 20% of BrS patie
Externí odkaz:
https://doaj.org/article/3110b987a88146039a487026877f7c4e
Autor:
Giovanni Peretto, Elena Sommariva, Chiara Di Resta, Martina Rabino, Andrea Villatore, Davide Lazzeroni, Simone Sala, Giulio Pompilio, Leslie T. Cooper
Publikováno v:
Biomolecules, Vol 13, Iss 4, p 646 (2023)
Over recent years, preclinical and clinical evidence has implicated myocardial inflammation (M-Infl) in the pathophysiology and phenotypes of traditionally genetic cardiomyopathies. M-Infl resembling myocarditis on imaging and histology occurs freque
Externí odkaz:
https://doaj.org/article/6ce0e586fa1e41c890e7caea35ecf539
Publikováno v:
Neural Regeneration Research, Vol 16, Iss 3, Pp 475-481 (2021)
Next generation sequencing is currently a cornerstone of genetic testing in routine diagnostics, allowing for the detection of sequence variants with so far unprecedented large scale, mainly in genetically heterogenous diseases, such as neurological
Externí odkaz:
https://doaj.org/article/d14a1b056a7d4d2dae77782441f974ae
Publikováno v:
Medicina, Vol 58, Iss 3, p 455 (2022)
Genetic carrier screening has been successfully used over the last decades to identify individuals at risk of transmitting specific DNA variants to their newborns, thus having an affected child. Traditional testing has been offered based on familial
Externí odkaz:
https://doaj.org/article/5e272238b15b4b4e83db213cb65772c0
Autor:
Nicolò Azzola Guicciardi, Michele De Bonis, Chiara Di Resta, Guido Ascione, Ottavio Alfieri, Francesco Maisano, Pasquale Vergara
Publikováno v:
Reviews in Cardiovascular Medicine, Vol 23, Iss 3, p 096 (2022)
Mitral valve prolapse (MVP) has a prevalence of 2–3% among the population. It involves a heterogeneous group of patients with different expressions and according to the phenotype can be further divided into fibroelastic deficiency, which is mainly
Externí odkaz:
https://doaj.org/article/9518c721bd824235bdce044d8b1a6519