Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Arianna Bisogno"'
Autor:
Alberto Battezzati, Andrea Foppiani, Gianfranco Alicandro, Arianna Bisogno, Arianna Biffi, Giorgio Bedogni, Simona Bertoli, Giulia De Carlo, Erica Nazzari, Carla Colombo
Publikováno v:
Endocrine Connections, Vol 11, Iss 5, Pp 1-10 (2022)
Objective: Diabetes is a frequent comorbidity in cystic fibrosis (CF), rela ted to multiple unfavorable outcomes. During the progression of β-cell dysfunction to diabetes, insulin deficiency could possibly reduce the anabolic support to grow ev en i
Externí odkaz:
https://doaj.org/article/d84258a4d2ac45fd875da8286fac12da
Autor:
Vito Terlizzi, Marco Lucarelli, Donatello Salvatore, Adriano Angioni, Arianna Bisogno, Cesare Braggion, Roberto Buzzetti, Vincenzo Carnovale, Rosaria Casciaro, Giuseppe Castaldo, Natalia Cirilli, Mirella Collura, Carla Colombo, Antonella Miriam Di Lullo, Ausilia Elce, Vincenzina Lucidi, Elisa Madarena, Rita Padoan, Serena Quattrucci, Valeria Raia, Manuela Seia, Lisa Termini, Federica Zarrilli
Publikováno v:
BMC Pulmonary Medicine, Vol 18, Iss 1, Pp 1-8 (2018)
Abstract Background A clinical heterogeneity was reported in patients with Cystic Fibrosis (CF) with the same CFTR genotype and between siblings with CF. Methods We investigated all clinical aspects in a cohort of 101 pairs of siblings with CF (inclu
Externí odkaz:
https://doaj.org/article/919080c9066b43f68e1a792c397b7dd0
Autor:
Carla Colombo, Arianna Bisogno, Andrea Foppiani, Erica Nazzari, Alessandro Leone, Andrea Mari, Valeria Daccò, Alberto Battezzati, A. Giana, Simone Gambazza
Publikováno v:
Journal of Endocrinological Investigation
Purpose The question whether the new cystic fibrosis transmembrane conductance regulator (CFTR) modulator drugs aimed at restoring CFTR protein function might improve glucose metabolism is gaining attention, but data on the effect of lumacaftor/ivaca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c55c60e2c49c5e587cda3b9c71131114
https://doi.org/10.1007/s40618-021-01525-4
https://doi.org/10.1007/s40618-021-01525-4
Autor:
Valeria Casavola, Arianna Bisogno, Sante Di Gioia, Onofrio Laselva, Carla Colombo, Lorenzo Guerra, Maria Favia, Massimo Conese
Publikováno v:
Expert Opinion on Drug Discovery. 15:873-891
Cystic Fibrosis (CF) is caused by mutations in theOnline databases were searched using key phrases for CF and CFTR modulators. Tezacaftor-ivacaftor treatment has proved to be safer than lumacaftor-ivacaftor, although clinical efficacy is similar. Fur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11a782b1d9b8701bf04b6fffe8d80e65
https://doi.org/10.1080/17460441.2020.1750592
https://doi.org/10.1080/17460441.2020.1750592
Summary Background & aims A higher mortality rate at young ages has been reported in cystic fibrosis (CF) girls compared to boys. The reasons of this gap remain unclear but may be related to a different evolution of the disease, in terms of growth an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44157cc8c295dd2609f15265492348ae
http://hdl.handle.net/11379/516298
http://hdl.handle.net/11379/516298
Autor:
Emilio F. Fossali, Alberto Battezzati, Silvia Bettocchi, Valentina De Cosmi, Alessandra Mazzocchi, Simona Bertoli, Carlo Agostoni, Arianna Bisogno, Edoardo Calderini, Carla Colombo, Michela Perrone, Giorgio Bedogni, Gregorio P. Milani, Alberto Edefonti
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 63:708-712
The resting energy expenditure (REE) of ill children is commonly estimated from prediction formulae developed in healthy children. The aim of the present study was to evaluate the accuracy of commonly employed REE prediction formulae versus indirect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c32bc8750b23e0d6af575c709e8f09fe
https://doi.org/10.1097/mpg.0000000000001223
https://doi.org/10.1097/mpg.0000000000001223
Autor:
Rita Padoan, Valeria Raia, Federica Zarrilli, Adriano Angioni, Cesare Braggion, Antonella Miriam Di Lullo, Serena Quattrucci, Donatello Salvatore, Giuseppe Castaldo, Mirella Collura, Vito Terlizzi, Natalia Cirilli, Manuela Seia, Rosaria Casciaro, Carla Colombo, Ausilia Elce, Vincenzina Lucidi, Vincenzo Carnovale, Marco Lucarelli, Roberto Buzzetti, Elisa Madarena, Arianna Bisogno, Lisa Termini
Publikováno v:
BMC Pulmonary Medicine
BMC Pulmonary Medicine, Vol 18, Iss 1, Pp 1-8 (2018)
BMC Pulmonary Medicine, Vol 18, Iss 1, Pp 1-8 (2018)
Background A clinical heterogeneity was reported in patients with Cystic Fibrosis (CF) with the same CFTR genotype and between siblings with CF. Methods We investigated all clinical aspects in a cohort of 101 pairs of siblings with CF (including 6 tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62609bee170708d9e15d87e43f72d6de
http://hdl.handle.net/11695/83497
http://hdl.handle.net/11695/83497
Autor:
Maria Luisa Bianchi, Arianna Bisogno, Fabiola Corti, Alberto Battezzati, Carla Colombo, Gianfranco Alicandro
Publikováno v:
Journal of Cystic Fibrosis. 13(3):328-334
Background In cystic fibrosis (CF), systemic inflammation and pulmonary infections sustain a catabolic response leading to fat free mass (FFM) depletion. Objectives To investigate the association between recurrent pulmonary exacerbations and alterati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::031499f96670ff4c00665da3950190fa
Autor:
Simone Gambazza, Carla Colombo, Arianna Bisogno, Valentina Montinaro, Susanna Esposito, Nicola Principi, Cristina Daleno, Valeria Daccò
Publikováno v:
Japanese Journal of Infectious Diseases. 67:399-401
Nasopharyngeal swabs obtained from 78 pediatric patients with cystic fibrosis (CF), including 47 with acute pulmonary exacerbation and 31 in a stable clinical condition, were evaluated for 17 respiratory viruses. Human rhinovirus (HRV) was the most f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba5016271d463ee752365a97b7dd8d40
https://doi.org/10.7883/yoken.67.399
https://doi.org/10.7883/yoken.67.399
Autor:
Alberto Battezzati, Silvana Loi, Chiara Speziali, Maria Luisa Bianchi, Carla Colombo, Arianna Bisogno, Gianfranco Alicandro
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 14(6)
Background The accuracy of body composition estimates based on skinfold thickness measurements and bioelectrical impedance analysis (BIA) is not yet adequately explored in cystic fibrosis (CF). Using DXA as reference method we verified the accuracy o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6fdee283123c7781e6bb25606219612
https://pubmed.ncbi.nlm.nih.gov/26282837
https://pubmed.ncbi.nlm.nih.gov/26282837