Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Ciro D'Orazio"'
Autor:
Paola Lecca, Marina Bertini, Roberta Vicentini, Emily Pintani, Ciro D’Orazio, Valeria Esposito, Karina Kleinfelder, Claudio Sorio, Paola Melotti
Publikováno v:
Proceedings of the XXth Conference of Open Innovations Association FRUCT, Vol 602, Iss 23, Pp 497-504 (2018)
Personalized medicine approach in cystic fibrosis (CF) is focusing on detection of cystic fibrosis transmembrane conductance regulator (CFTR) function in single patients and standardized outcomes for CFTR function in vivo. We applied Optical Sweat
Externí odkaz:
https://doaj.org/article/f0f0e868813b4e2ba389d6bf208d92a0
Autor:
Cinzia Scambi, Lucia De Franceschi, Patrizia Guarini, Fabio Poli, Angela Siciliano, Patrizia Pattini, Andrea Biondani, Valentina La Verde, Oscar Bortolami, Francesco Turrini, Franco Carta, Ciro D'Orazio, Baroukh M Assael, Giovanni Faccini, Lisa M Bambara
Publikováno v:
PLoS ONE, Vol 4, Iss 3, p e4782 (2009)
Cystic fibrosis (CF) is one of the most common fatal autosomal recessive disorders in the Caucasian population caused by mutations of gene for the cystic fibrosis transmembrane conductance regulator (CFTR). New experimental therapeutic strategies for
Externí odkaz:
https://doaj.org/article/2538d0a6dfbd40b9ad833858e4dbdda1
Autor:
Ciro, D'Orazio, Padoan, Rita, Blau, Hannah, Marostica, Anna, Fuoti, Maurizio, Volpi, Sonia, Pilotta, Alba, Meyerovitch, Joseph, Sher, Daniel, Assael, Baroukh M.
Publikováno v:
In Journal of Cystic Fibrosis August 2012
Autor:
Ferenc Karpati, L.E. Jenkins, D.M. Cox, Yvonne Belessis, Carla Federica Bortoluzzi, L. Da Dalt, Baroukh M. Assael, Ciro D'Orazio, Stéphanie Bui, V. Švabe, J.C. Dubus, L. Honková, A. Jung, Tanja Pressler, M. Geerdink, Phil Robinson, C. Vazquez, Rosaria Casciaro, Valeria Raia, A.J.M. Reid, C. Mainguy, Daan Caudri, Antonella Tosco, S. Rovira, M.C. Cavicchi, Eleonora Pontello, O. Sepe, Stephen M. Stick, A. Tai, Silvia Gartner, Paolo Rossi, M. G. Myriam Hunink, Veronika Skalická, Harm A.W.M. Tiddens, C.R. Hansen, A. Möller, Emily Pintani, Karin M. de Winter-de Groot, A.S. Neri, E. Rietschel, André Schultz, F. De Gregorio, Marijke Proesmans, F. Bremont, Paul Robinson
Publikováno v:
Journal of Cystic Fibrosis, 19(4), 641-646. Elsevier
Background Recent standards of care mention chest radiography (CR) but not chest computed tomography (CT) in routine annual follow-up of children with cystic fibrosis (CF). To minimise radiation risk, CT or CR should only be performed if they impact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ebbc725b4af89aebcda619690db28c4
https://doi.org/10.1016/j.jcf.2019.08.005
https://doi.org/10.1016/j.jcf.2019.08.005
Autor:
Baroukh M. Assael, Eleonora Zavatti, Teresinha Leal, Roberta Rizzo, Paola Melotti, Loredana Melchiorri, Emily Pintani, Gabriella Bergamini, Ciro D'Orazio, Daria Bortolotti, Claudio Sorio
Publikováno v:
Future Microbiology. 11:363-373
Background: Deregulated immune response fails to control biofilm-forming bacteria, as Pseudomonas aeruginosa, in the lungs of cystic fibrosis (CF) patients. HLA-G is an immune-modulatory molecule involved in respiratory diseases and infections. Mater
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bac1793e2036bbc6c0f001088082da1f
https://doi.org/10.2217/fmb.15.143
https://doi.org/10.2217/fmb.15.143
Autor:
Lecca, Paola, Bertini, Marina, Vicentini, Roberta, Pintani, Emily, Ciro, D'Orazio, Esposito, Valeria, Kleinfelder, Karina, Sorio, Claudio, Melotti, Paola
Publikováno v:
Proceedings of the XXth Conference of Open Innovations Association FRUCT, Vol 602, Iss 23, Pp 497-504 (2018)
Personalized medicine approach in cystic fibrosis (CF) is focusing on detection of cystic fibrosis transmembrane conductance regulator (CFTR) function in single patients and standardized outcomes for CFTR function in vivo. We applied Optical Sweat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cc265abc6ea679602de08d1e390c7d5
Autor:
Gloria Tridello, Ciro D'Orazio, Carla-Federica Bortoluzzi, Baroukh M. Assael, Harm A.W.M. Tiddens, Sonia Volpi, Martine Loeve
Publikováno v:
Journal of Cystic Fibrosis. 13:564-571
BackgroundChildren with cystic fibrosis (CF) are often Pseudomonas aeruginosa (PsA) free and exhibit normal spirometry between the ages of 5 and 7. It is reported that computed tomography (CT) is more sensitive than FEV1 as an instrument in the ident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9db2ea6ad71fcdf6e209bbaec27049f9
https://doi.org/10.1016/j.jcf.2014.03.006
https://doi.org/10.1016/j.jcf.2014.03.006
Autor:
Luigi Lubrano, Ciro D'Orazio, Carlo Castellani, Elisa Andreatta, Corrado Vassanelli, L. Menin, Sonia Volpi
Publikováno v:
7.3 Cystic Fibrosis.
Introduction: Lung clearance index (LCI) is a very sensitive marker of early lung disease in Cystic Fibrosis (CF). In Cystic Fibrosis Screen Positive Inconclusive Diagnosis (CFSPID) and in compound heterozygotes carrying at least one mutation with in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f81e26dd17859255864d830bf6e00d19
https://doi.org/10.1183/13993003.congress-2016.oa1489
https://doi.org/10.1183/13993003.congress-2016.oa1489
Autor:
Antonella Borruso, Corrado Vassanelli, Ugo Pradal, Luigi Lubrano, Ciro D'Orazio, Sonia Volpi, Elena Spinelli, Elisa Andreatta
Publikováno v:
7.2 Paediatric Asthma and Allergy.
INTRODUCTION Over the last decade the study of pulmonary function by multiple breath washout technique (MBW) has been widely used to detect early pulmonary changes in Cystic Fibrosis. On the contrary there are only few studies that use Lung Clearance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64fb6e0ce01f50b4709c45dc315a5b79
https://doi.org/10.1183/13993003.congress-2016.pa4372
https://doi.org/10.1183/13993003.congress-2016.pa4372
Autor:
Maria Lucia Furnari, Alberto Dal Molin, Anna Maria Oneta, Sofia Bisogni, Cesare Braggion, Dino Stefano Di Massimo, B. Messore, Maria Vittoria Di Toppa, Gabriella Festa, Filippo Festini, G. Tuccio, Serena Rampini, Maria Luisa Zunino, F. Alghisi, Carla Colombo, Ciro D'Orazio, Elena Rizzi, Vincenzo Spadea, Bianca Grosso, Simona Cristadoro, Maria Antonietta Calamia, Vincenzo Carnovale
Publikováno v:
The Journal of Vascular Access. 13:290-295
The aim of this study was to assess the incidence of late onset complications of totally implantable venous access devices (TIVAD) in patients with cystic fibrosis (CF) and to investigate possible associations between the rate of complications and di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef02420b69361a396ca58c6981cb4060
https://doi.org/10.5301/jva.5000036
https://doi.org/10.5301/jva.5000036