Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Stefania Ottaviani"'
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, Vol 23, Iss 17, p 9859 (2022)
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
Externí odkaz:
https://doaj.org/article/c5e50b355ee1434981f07b93ff88fd17
Autor:
Riccardo Ronzoni, Ilaria Ferrarotti, Emanuela D’Acunto, Alice M. Balderacchi, Stefania Ottaviani, David A. Lomas, James A. Irving, Elena Miranda, Annamaria Fra
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 11, p 5668 (2021)
Alpha-1-antitrypsin (AAT) deficiency causes pulmonary disease due to decreased levels of circulating AAT and consequently unbalanced protease activity in the lungs. Deposition of specific AAT variants, such as the common Z AAT, within hepatocytes may
Externí odkaz:
https://doaj.org/article/60628c5796ca46fe8964acc684f1df3e
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
Publikováno v:
Breathe, Vol 14, Iss 2, Pp e17-e24 (2018)
α1-Antitrypsin deficiency (AATD) is an inherited metabolic disorder in which mutations in the coding sequence of the SERPINA1 gene prevent secretion of α1-antitrypsin (α1-AT) and cause predisposition to pulmonary and liver diseases. The heterogene
Externí odkaz:
https://doaj.org/article/5be70340a36549e6927736e082e5c7f6
Autor:
Ilaria Ferrarotti, Beata Poplawska-Wisniewska, Maria Teresa Trevisan, Janine Koepke, Marc Dresel, Rembert Koczulla, Stefania Ottaviani, Raffaele Baldo, Marina Gorrini, Giorgia Sala, Luana Cavallon, Tobias Welte, Joanna Chorostowska-Wynimko, Maurizio Luisetti, Sabina Janciauskiene
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0135316 (2015)
The Z deficiency in α1-antitrypsin (A1ATD) is an under-recognized condition. Alpha1-antitrypsin (A1AT) is the main protein in the α1-globulin fraction of serum protein electrophoresis (SPE); however, evaluation of the α1-globulin protein fraction
Externí odkaz:
https://doaj.org/article/8cb75f527a694be68b1783b47bf047c0
Autor:
Gian-Andri Thun, Ilaria Ferrarotti, Medea Imboden, Thierry Rochat, Margaret Gerbase, Florian Kronenberg, Pierre-Olivier Bridevaux, Elisabeth Zemp, Michele Zorzetto, Stefania Ottaviani, Erich W Russi, Maurizio Luisetti, Nicole M Probst-Hensch
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e42728 (2012)
BackgroundSevere alpha1-antitrypsin (AAT) deficiency is a strong risk factor for COPD. But the impact of gene variants resulting in mild or intermediate AAT deficiency on the longitudinal course of respiratory health remains controversial. There is i
Externí odkaz:
https://doaj.org/article/8a8db7f7e3fa49bfa3d0094019fde0c5
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.