Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Aaron Chidekel"'
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2023)
BackgroundChildren with Trisomy 21 (T21) are at an increased risk of sleep-disordered breathing (SDB), which can impact daily functioning and cause other health complications. Accordingly, it is imperative to diagnose and treat SDB in this population
Externí odkaz:
https://doaj.org/article/57ddf849ffab4dbdad4ad688da95b4a6
Publikováno v:
Respiratory Medicine Case Reports, Vol 40, Iss , Pp 101775- (2022)
Elexacaftor-tezacaftor-ivacaftor (ELX/TEZ/IVA) is a triple combination drug therapy approved for individuals with cystic fibrosis (CF) who possess at least one copy of the F508del cystic fibrosis transmembrane conductance regulator (CFTR) variant. EL
Externí odkaz:
https://doaj.org/article/994ca96745ef4a1192ee5458994862df
Autor:
Ambika Shenoy, Dina Spyropoulos, Kathleen Peeke, Dawn Smith, Michael Cellucci, Aaron Chidekel
Publikováno v:
International Journal of Neonatal Screening, Vol 7, Iss 1, p 1 (2020)
Newborn screening (NBS) for Cystic Fibrosis (CF) has revolutionized the diagnosis of this inherited disease. CF NBS goals are to identify, diagnose, and initiate early CF treatment to attain better health outcomes. Abnormal CF NBS infants require dia
Externí odkaz:
https://doaj.org/article/7695f1e6fcf8400189051128b825005d
Publikováno v:
Pulmonary Medicine, Vol 2012 (2012)
Humidification of inspired gas is important for patients receiving respiratory support. High-flow nasal cannula (HFNC) effectively provides temperature and humidity-controlled gas to the airway. We hypothesized that various levels of gas humidificati
Externí odkaz:
https://doaj.org/article/2d7e36f6e4364d5ca810db65813b83bc
Publikováno v:
Critical Care Research and Practice, Vol 2010 (2010)
This article reviews the application of the human airway Calu-3 cell line as a respiratory model for studying the effects of gas concentrations, exposure time, biophysical stress, and biological agents on human airway epithelial cells. Calu-3 cells a
Externí odkaz:
https://doaj.org/article/e00a308926294145bbb3d4d0f149e749
Publikováno v:
SLEEP. 46:A352-A353
Introduction There is a paucity of literature regarding “flagged PSGs”, a term used to triage emergent PSGs for expedited scoring and reporting. Given the morbidity and multi organ-system dysfunction of untreated OSAS in children, it is extremely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a5807c4bf74c324640f65caad0d3920
https://doi.org/10.1093/sleep/zsad077.0800
https://doi.org/10.1093/sleep/zsad077.0800
Autor:
Abigail Strang, Kimberly S. Canter, Katherine Okonak, Sophie Wilks, Aaron Chidekel, Janet A. Deatrick, Dana Geiser, Melanie Franklin
Publikováno v:
Journal of Clinical Psychology in Medical Settings. 29:44-53
Evidence suggests that individuals with Cystic Fibrosis (CF) experience difficulties with sleep architecture and hygiene, although research is limited. There are currently no behavioral sleep interventions for youth with CF. The current study used qu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3cfb832d7394427413665cde400d740
https://doi.org/10.1007/s10880-021-09774-4
https://doi.org/10.1007/s10880-021-09774-4
Publikováno v:
SLEEP. 46:A346-A346
Introduction High quality sleep is crucial to health and development in children. Compared to healthy children, hospitalized children have a higher chance of experiencing disrupted and poor-quality sleep, which may thereby impede their recovery. Ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c090f7011675e6ffb5cdf95d85aec0b
https://doi.org/10.1093/sleep/zsad077.0784
https://doi.org/10.1093/sleep/zsad077.0784
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
Youth with CF are at increased risk for physiological and behavioral sleep difficulties due to disease-specific symptoms and more general pediatric sleep challenges. Despite evidence suggesting that behavioral sleep interventions are effective for im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52c5dd3c11c8270fa6bced2cfc7180a1
https://pubmed.ncbi.nlm.nih.gov/35871972
https://pubmed.ncbi.nlm.nih.gov/35871972
Publikováno v:
Paediatric Respiratory Reviews. 36:15-24
Pulmonary lymphatic disorders are characterized by the presence of the abnormal lymphatic tissues in the thoracic cavity, presenting clinically as chylothorax, chylopericardium, chyloptysis, interstitial lung disease and plastic bronchitis. These con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeef535ab5b93a3fac53afee4ed05747
https://doi.org/10.1016/j.prrv.2020.07.001
https://doi.org/10.1016/j.prrv.2020.07.001