Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Anna Cassano"'
Autor:
Carlotta Lambertini, Annamaria Grandis, Margherita De Silva, Ilaria Anna Cassano, Stefano Checcacci Carboni, Noemi Romagnoli
Publikováno v:
Animals, Vol 13, Iss 1, p 156 (2022)
The Spritztube (ST) is an extraglottic airway device developed for humans. The aim of the study was to design an ST for rabbits and to evaluate its feasibility. The study was divided into two phases. Phase I: anatomical study on 12 rabbit cadavers to
Externí odkaz:
https://doaj.org/article/19a50d3f41be4b6e994cb1536b782564
Autor:
Silvano Dragonieri, Mario Francesco Damiani, Alberto Capozzolo, Pierluigi Carratù, Onofrio Resta, Anna Cassano, Vitaliano Nicola Quaranta
Publikováno v:
Neurodegenerative Diseases. 17:14-21
Background/Objective: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by the progressive loss of central and peripheral motor neurons. Some studies have found discordant data in the presence of sleep apnea in ALS pati
Autor:
Mariangela Tedone, Anna Cassano, Onofrio Resta, Salvatore Dongiovanni, Francesco Fanfulla, Felice Gadaleta, Pierluigi Carratù
Publikováno v:
Amyotrophic Lateral Sclerosis. 12:458-463
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that rapidly involves the respiratory system, leading to persistent respiratory insufficiency. Neuromuscular respiratory weakness is also responsible for sleep disordered breathing (S
Autor:
Rosanna Tortelli, Giancarlo Logroscino, Francesco Panza, Rosa Capozzo, Vitaliano Nicola Quaranta, Massimiliano Copetti, Vito Antonio Falcone, Fabio Pellegrini, Andrea Fontana, Anna Cassano, Isabella Laura Simone, Rosa Cortese, Onofrio Resta, Pierluigi Carratù
Publikováno v:
Journal of neurology. 262(3)
Forced vital capacity (FVC) shows limitations in detecting respiratory failure in the early phase of amyotrophic lateral sclerosis (ALS). In fact, mild-to-moderate respiratory muscle weakness may be present even when FVC is normal, and ALS patients w
Autor:
Donato Lacedonia, Onofrio Resta, Felice Gadaleta, Pierluigi Carratù, Lucia Spicuzza, Anna Cassano, Ester Boniello, Giuseppe Di Maria, Cristina Scoditti, Mauro Maniscalco
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 4, Iss 1, p 10 (2009)
Orphanet Journal of Rare Diseases, Vol 4, Iss 1, p 10 (2009)
Background Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease, which rapidly leads to chronic respiratory failure requiring mechanical ventilation. Currently, forced vital capacity (FVC) < 50% is considered as physiologic marker for a