Zobrazeno 1 - 10
of 168
pro vyhledávání: '"Athanasios G, Kaditis"'
Autor:
Anastasia Polytarchou, Angeliki Moudaki, Eli Van de Perck, An Boudewyns, Athanasios G. Kaditis, Stijn Verhulst, Refika Ersu
Publikováno v:
European Respiratory Review, Vol 33, Iss 171 (2024)
The aim of this review is to summarise evidence that became available after publication of the 2017 European Respiratory Society statement on the diagnosis and management of obstructive sleep apnoea syndrome (OSAS) in 1- to 23-month-old children. The
Externí odkaz:
https://doaj.org/article/2a1885ba8418463588acc76d200bb9e7
Autor:
Matthias Griese, Panagiota Panagiotou, Effrosyni D. Manali, Mirjam Stahl, Nicolaus Schwerk, Vanessa Costa, Konstantinos Douros, Maria Kallieri, Ruth Maria Urbantat, Horst von Bernuth, Lykourgos Kolilekas, Lurdes Morais, Ana Ramos, Kerstin Landwehr, Katrin Knoflach, Florian Gothe, Karl Reiter, Vassiliki Papaevangelou, Athanasios G. Kaditis, Christina Kanaka-Gantenbein, Spyros A. Papiris
Publikováno v:
ERJ Open Research, Vol 8, Iss 1 (2022)
In childhood, a multitude of causes lead to pulmonary alveolar proteinosis (PAP), an excessive surfactant accumulation in the alveolar space, limiting gas exchange. Autoantibodies against granulocyte–macrophage colony-stimulating factor (GM-CSF) ca
Externí odkaz:
https://doaj.org/article/80e55b59b9a04dfdb1567d9a0288e94f
Publikováno v:
Children, Vol 9, Iss 12, p 1898 (2022)
Inflammation and infection play an important role in the pathophysiology of cystic fibrosis, and they are significant causes of morbidity and mortality in CF. The presence of thick mucus in the CF airways predisposes to local hypoxia and promotes inf
Externí odkaz:
https://doaj.org/article/e9487d4683324dabad1102a6b70c178f
Publikováno v:
Children, Vol 9, Iss 8, p 1207 (2022)
Spinal muscular atrophy (SMA) is a genetic neuromuscular disease resulting in global muscular weakness and, frequently, in respiratory failure and premature death. Gene-based therapies like Nusinersen are now available for patients with SMA. The aim
Externí odkaz:
https://doaj.org/article/561a740c3bfd4c69badd941e05f1f419
Autor:
Dimitrios Moutafidis, Maria Gavra, Sotirios Golfinopoulos, Antonios Kattamis, George Chrousos, Christina Kanaka-Gantenbein, Athanasios G. Kaditis
Publikováno v:
Children, Vol 8, Iss 12, p 1172 (2021)
In contrast to studies of adults with emphysema, application of fixed thresholds to determine low- and high-attenuation areas (air-trapping and parenchymal lung disease) in pediatric quantitative chest CT is problematic. We aimed to assess age effect
Externí odkaz:
https://doaj.org/article/4ea61abe1cc245088dae70a79031f0e3
Autor:
Athanasios G. Kaditis, James Acton, Connie Fenton, Leila Kheirandish-Gozal, Zarah Ner, Rebekah Nevel, David Gozal, Adrienne Ohler
Publikováno v:
Chest.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bebddc964b7b8da198ee250e00dc2b30
https://doi.org/10.1016/j.chest.2023.05.024
https://doi.org/10.1016/j.chest.2023.05.024
Autor:
Dimitrios Poulimeneas, Maria G. Grammatikopoulou, Argyri Petrocheilou, Athanasios G. Kaditis, Tonia Vassilakou
Publikováno v:
Children, Vol 7, Iss 12, p 269 (2020)
Malnutrition prevails in considerable proportions of children with Cystic Fibrosis (CF), and is often associated with adverse outcomes. For this, routine screening for malnutrition is pivotal. In the present cross-sectional study, we aimed to assess
Externí odkaz:
https://doaj.org/article/d2cec205e9054b25a9fef7dd3bfc2798
Autor:
Hui-Leng Tan, Athanasios G Kaditis
Publikováno v:
Sleep.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55111324df46858f00517099054bc473
https://doi.org/10.1093/sleep/zsad040
https://doi.org/10.1093/sleep/zsad040
Publikováno v:
ERS Handbook of Respiratory Sleep Medicine ISBN: 9781849841634
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b4e24567081ed234f3afe93ad2230f1
https://doi.org/10.1183/9781849841641.015222_5
https://doi.org/10.1183/9781849841641.015222_5
Publikováno v:
Children, Vol 7, Iss 10, p 153 (2020)
Nebulizers are used by the great majority of cystic fibrosis patients for delivery of cornerstone treatments. Inhalation technique and adequate disinfection and maintenance are important for optimizing medication delivery. In this study, inhalation t
Externí odkaz:
https://doaj.org/article/4bc5fabab44e4bbb91c4f61e23a1e71a