Zobrazeno 1 - 10
of 234
pro vyhledávání: '"Valeria, Raia"'
Autor:
Natalia Cirilli, Giovanna Floridia, Annalisa Amato, Rita Padoan, Federica Censi, Gianluca Ferrari, Valeria Raia, Giuseppe Castaldo, Ettore Capoluongo, Domenica Taruscio, Marco Salvatore
Publikováno v:
Practical Laboratory Medicine, Vol 40, Iss , Pp e00403- (2024)
Background: The advent of CFTR modulators highlighted that the sweat test (ST) for CF can be used also as an outcome measure for the basic defect of CFTR. Despite the technological advances, ST still remains operator-dependent and its execution shoul
Externí odkaz:
https://doaj.org/article/d9d14bf9cbc149d883b03e6effb564da
Autor:
Angela Sepe, Camilla Romano, Ivana Landi, Alice Castaldo, Chiara Cimbalo, Federica Farina, Manuela Scorza, Laura Salvadori, Valeria Raia, Antonella Tosco
Publikováno v:
Clinical Case Reports, Vol 11, Iss 11, Pp n/a-n/a (2023)
Key Clinical Message The introduction of newborn screening for cystic fibrosis (CF) increased diagnosis of cystic fibrosis screen positive inconclusive diagnosis (CFSPID). We described the case of a 12‐month‐old boy with CFSPID who, during summer
Externí odkaz:
https://doaj.org/article/1cadc514f4d44472a778ac7d425ce614
Autor:
Luca Occhigrossi, Federica Rossin, Valeria Rachela Villella, Speranza Esposito, Carlo Abbate, Manuela D’Eletto, Maria Grazia Farrace, Antonella Tosco, Roberta Nardacci, Gian Maria Fimia, Valeria Raia, Mauro Piacentini
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Cystic fibrosis (CF) is a rare autosomal recessive disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The most common mutation is F508del-CFTR (ΔF) which leads the encoded ion channel towards misfoldi
Externí odkaz:
https://doaj.org/article/7f5505c5364c46dbb11974be90ac7257
Autor:
Sonia Volpi, Vincenzo Carnovale, Carla Colombo, Valeria Raia, Francesco Blasi, Giovanni Pappagallo, PULMOCARE TEAM
Publikováno v:
Health Science Reports, Vol 5, Iss 4, Pp n/a-n/a (2022)
Abstract Background The goal of mucoactive therapies in cystic fibrosis (CF) is to enhance sputum clearance and to reduce a progressive decline in lung function over the patient's lifetime. We aimed to investigate the level of consensus among special
Externí odkaz:
https://doaj.org/article/a0efc3f6584d44ef94a25cf714e2611b
Autor:
Francesco Maria Rosanio, Enza Mozzillo, Chiara Cimbalo, Alberto Casertano, Angela Sepe, Valeria Raia, Adriana Franzese, Antonella Tosco
Publikováno v:
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-5 (2021)
Abstract Background Cystic Fibrosis Related Diabetes (CFRD) is a frequent comorbidity of patients with Cystic Fibrosis (CF). A worsening of clinical conditions appears before CFRD. It has been demonstrated a decline in pulmonary function and nutritio
Externí odkaz:
https://doaj.org/article/0411a41b830d46a89557894c9cc9fa26
Autor:
Grazia Isabella Continisio, Nicola Serra, Assunta Guillari, Maria Teresa Civitella, Angela Sepe, Silvio Simeone, Gianpaolo Gargiulo, Silvia Toscano, Maria Rosaria Esposito, Valeria Raia, Teresa Rea
Publikováno v:
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-9 (2020)
Abstract Background The management of chronic diseases, particularly in children, requires an integrated physical and psychological approach to both sick children and their family. This is the case of Cystic Fibrosis (CF), a complex genetic chronic d
Externí odkaz:
https://doaj.org/article/67ff4b2e04a744a8aff7ef6c6c2aeab8
Autor:
Anna Maria Iannicelli, Daniele Vito, Concetta Anna Dodaro, Pasquale De Matteo, Rita Nocerino, Angela Sepe, Valeria Raia
Publikováno v:
Italian Journal of Pediatrics, Vol 45, Iss 1, Pp 1-6 (2019)
Abstract Virtual Reality (VR) as a tool for pain reduction is the research topic of several clinical trial for Randomized Controlled Trials despite its wide use in the daily clinical practice for non- pharmacological reduction of pain in some countri
Externí odkaz:
https://doaj.org/article/914861e8f7a34e9ca059612938c6b3d3
Autor:
Claudia Piona, Enza Mozzillo, Antonella Tosco, Sonia Volpi, Francesco Maria Rosanio, Chiara Cimbalo, Adriana Franzese, Valeria Raia, Chiara Zusi, Federica Emiliani, Maria Linda Boselli, Maddalena Trombetta, Riccardo Crocina Bonadonna, Marco Cipolli, Claudio Maffeis
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 14, p 4149 (2022)
Background: To date, no consistent data are available on the possible impact of CFTR modulators on glucose metabolism. The aim of this study was to test the hypothesis that treatment with CFTR modulators is associated with an improvement in the key d
Externí odkaz:
https://doaj.org/article/404d4522c5764f43998247365044e474
Publikováno v:
Italian Journal of Pediatrics, Vol 45, Iss 1, Pp 1-4 (2019)
Abstract Familial loss-of-function mutations of the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) channel protein cause cystic fibrosis (CF), the most frequent inherited life-threatening disease in the Caucasian popul
Externí odkaz:
https://doaj.org/article/df83cbe9bbd4479bb7da7264e80f1748
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