Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Valentina Barzon"'
Autor:
Ardak Zhumagaliyeva, Stefania Ottaviani, Timm Greulich, Marina Gorrini, Claus Vogelmeier, Ludmila Karazhanova, Gulmira Nurgazina, Annalisa DeSilvestri, Victor Kotke, Valentina Barzon, Michele Zorzetto, Angelo Corsico, Ilaria Ferrarotti
Publikováno v:
Multidisciplinary Respiratory Medicine, Vol 12, Iss 1, Pp 1-8 (2017)
Abstract Background Alpha-1-antitrypsin deficiency (AATD) is an under-diagnosed condition in patients with chronic obstructive pulmonary disease (COPD). The aim of this study was to screen for AATD in Kazakh patients with COPD using dried blood spot
Externí odkaz:
https://doaj.org/article/97861dcd9aaa424f96b56faba20a469b
Autor:
Elia Bari, Ilaria Ferrarotti, Dario Di Silvestre, Pietro Grisoli, Valentina Barzon, Alice Balderacchi, Maria Luisa Torre, Rossana Rossi, Pierluigi Mauri, Angelo Guido Corsico, Sara Perteghella
Publikováno v:
Cells, Vol 8, Iss 9, p 965 (2019)
Accumulating evidence shows that Mesenchymal Stem/Stromal Cells (MSCs) exert their therapeutic effects by the release of secretome, made of both soluble proteins and nano/microstructured extracellular vesicles (EVs). In this work, for the first time,
Externí odkaz:
https://doaj.org/article/97111b4be7b84ef5abf6f38943535f11
Autor:
Davide PILONI, Stefania OTTAVIANI, Laura SADERI, Luciano CORDA, Paolo BADERNA, Valentina BARZON, Alice M. BALDERACCHI, Christine SEEBACHER, Bruno BALBI, Federica ALBICINI, Alessandra CORINO, Maria C. MENNITTI, Claudio TIRELLI, Fabio SPREAFICO, Matteo BOSIO, Francesca MARIANI, Giovanni SOTGIU, Angelo G. CORSICO, Ilaria FERRAROTTI
Publikováno v:
Minerva Medica.
Autor:
Valentina Barzon, Alessandra Corino, Ilaria Ferrarotti, Angelo Corsico, Alice Maria Balderacchi, Michele Zorzetto, Stefania Ottaviani, Marion Wencker
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM). 59:1384-1391
Objectives Alpha1-antitrypsin deficiency (AATD) is an inherited condition that predisposes individuals to an increased risk of developing lung and liver disease. Even though AATD is one of the most widespread inherited diseases in Caucasian populatio
Autor:
Ilaria Ferrarotti, Angelo Corsico, Francesca Mariani, Deborah Ambruoso, Alice Maria Balderacchi, Davide Piloni, Alessandra Corino, Claudio Tirelli, Valentina Barzon, Stefania Ottaviani
Publikováno v:
Monitoring airway disease.
Autor:
Stefania Ottaviani, Ilaria Ferrarotti, Francesca Mariani, Alice Maria Balderacchi, Alessandra Corino, Angelo Corsico, Valentina Barzon, Davide Piloni, Annalisa De Silvestri
Publikováno v:
Epidemiology.
Autor:
Valentina Barzon, Stefania Ottaviani, Alice Maria Balderacchi, Alessandra Corino, Davide Piloni, Giulia Accordino, Manuela Coretti, Francesca Mariani, Angelo Guido Corsico, Ilaria Ferrarotti
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 17; Pages: 9859
Alpha1-antitrypsin (AAT) is a serine protease inhibitor that is encoded by the highly polymorphic SERPINA1 gene. Mutations in this gene can lead to AAT deficiency (AATD), which is associated with an increased risk of lung and/or liver disease. On the
Autor:
Ilaria Ferrarotti, Stefania Ottaviani, Francesca Mariani, Bruno Balbi, Alessandra Corino, Valentina Barzon, Alice Maria Balderacchi, Angelo Corsico, Davide Piloni
Publikováno v:
Monitoring airway disease.
Autor:
Valentina Barzon, Amaia Larruskain, Marina Gorrini, Marco Antiga, Rachid El Hamss, Ilaria Ferrarotti, Stefania Ottaviani, Amaya Buxens, Angelo Corsico
Publikováno v:
Journal of Clinical Laboratory Analysis
Background: Alpha-1 antitrypsin deficiency (AATD) is an under-diagnosed hereditary disorder characterized by reduced serum levels of alpha-1 antitrypsin (AAT) and increased risk to develop lung and liver diseases at an early age. AAT is encoded by th
Autor:
Ilaria Ferrarotti, Angelo Corsico, Valentina Barzon, Noel Gerard Mc Elvaney, Stefania Ottaviani, Alice Maria Balderacchi, Anna M. Fra, Davide Piloni, Tomás P. Carroll, Francesca Mariani
Background: Alpha-1 antitrypsin (AAT) is a serine protease inhibitor, encoded by the highly polymorphic SERPINA1 gene. Mutations in the SERPINA1 gene can lead to AAT deficiency (AATD), which is associated with a substantially increased risk of lung a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9020d78754ef2979706c1ff64d9b03c
http://hdl.handle.net/11379/538807
http://hdl.handle.net/11379/538807