Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Sheila S. Kun"'
Autor:
Ajay S. Kasi, Melinda Riccitelli, Sheila S. Kun, Adrianna L. Westbrook, George L. Silva, Thomas G. Keens, Lokesh Guglani
Publikováno v:
Pediatric Allergy, Immunology, and Pulmonology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5da7d0a03c72c2f5e72677ae6af521dc
https://doi.org/10.1089/ped.2023.0004
https://doi.org/10.1089/ped.2023.0004
Autor:
Gloria Y. Chang, Tate Salazar, Abhishek Karnwal, Sheila S. Kun, Josephine Ellashek, Cathy E. Shin, J. Gordon McComb, Thomas G. Keens, Iris A. Perez
Publikováno v:
Sleep and Breathing. 27:505-510
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6f9013ecea171d81e044b6ed9d9afc7
https://doi.org/10.1007/s11325-022-02632-z
https://doi.org/10.1007/s11325-022-02632-z
Autor:
A. Ioana Cristea, Clement L. Ren, Reshma Amin, Laurie C. Eldredge, Jonathan C. Levin, Parevi P. Majmudar, Anne E. May, Rebecca S. Rose, Michael C. Tracy, Karen F. Watters, Julian Allen, Eric D. Austin, Mary E. Cataletto, Joseph M. Collaco, Robert J. Fleck, Andrew Gelfand, Don Hayes, Marcus H. Jones, Sheila S. Kun, Erica W. Mandell, Sharon A. McGrath-Morrow, Howard B. Panitch, Rizwana Popatia, Lawrence M. Rhein, Alejandro Teper, Jason C. Woods, Narayan Iyer, Christopher D. Baker
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 204:e115-e133
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d0f6455f8013286ff09352f122ebf88
https://doi.org/10.1164/rccm.202110-2269st
https://doi.org/10.1164/rccm.202110-2269st
Autor:
Gloria Y, Chang, Tate, Salazar, Abhishek, Karnwal, Sheila S, Kun, Josephine, Ellashek, Cathy E, Shin, J Gordon, McComb, Thomas G, Keens, Iris A, Perez
Publikováno v:
Sleepbreathing = SchlafAtmung.
Patients with congenital central hypoventilation syndrome (CCHS) have autonomic dysfunction and lack ventilatory responses to hypoxemia and hypercarbia and thus are prone to adverse events during general anesthesia. The objective of this study was to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ebea5ce2697202de80dea6d69232f875
https://pubmed.ncbi.nlm.nih.gov/35554785
https://pubmed.ncbi.nlm.nih.gov/35554785
Publikováno v:
Expert Review of Respiratory Medicine. 12:283-292
Congenital central hypoventilation syndrome (CCHS) is a rare disorder defined by a failure in autonomic control of breathing secondary to mutations of the PHOX2B gene. Affected individuals demonstrate absent or diminished physiologic response to hype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc92fca821482130faa5ad1f5549aa33
https://doi.org/10.1080/17476348.2018.1445970
https://doi.org/10.1080/17476348.2018.1445970
Autor:
Glenn Takata, Sally L. Davidson Ward, Thomas G. Keens, Alexis Deavenport-Saman, Sheila S. Kun
Publikováno v:
Respiratory care. 64(12)
BACKGROUND: There is limited knowledge of rapid-response (RR) events and code events for children receiving home mechanical ventilation (HMV) via a tracheostomy in a non-ICU respiratory care unit. The purpose of this study was to describe the demogra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77384637ce2467950fcb10794a117d63
https://pubmed.ncbi.nlm.nih.gov/31767687
https://pubmed.ncbi.nlm.nih.gov/31767687
PHOX2B 20/27 polyalanine repeat mutation (PARM) in patients with congenital central hypoventilation syndrome (CCHS) is generally associated with full-time ventilator dependence, Hirschsprung disease, and increased risk for cardiac asystole. We follow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f9eab2efcbaf650a61910851ce80f24
https://europepmc.org/articles/PMC6287728/
https://europepmc.org/articles/PMC6287728/
Publikováno v:
Pediatric Health, Medicine and Therapeutics
Congenital central hypoventilation syndrome (CCHS) is a rare genetic disorder with failure of central control of breathing and of the autonomic nervous system function due to a mutation in the paired-like homeobox 2B (PHOX2B) gene. Affected patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c58d936db37f97b28863bf14dc3eebc
https://doi.org/10.2147/phmt.s95054
https://doi.org/10.2147/phmt.s95054
Publikováno v:
Journal of Clinical Sleep Medicine. 13:925-927
PHOX2B non-polyalanine repeat mutation (NPARM) in patients with congenital central hypoventilation syndrome (CCHS) is generally considered to be associated with full-time ventilator dependence and severe autonomic nervous system dysfunction. We repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8f574244a4bdf1c08642c10e11a898c
https://doi.org/10.5664/jcsm.6670
https://doi.org/10.5664/jcsm.6670
Publikováno v:
Sleep. 43:A333-A333
Introduction Congenital Central Hypoventilation Syndrome (CCHS) requires lifelong ventilatory support during sleep. CCHS patients are vulnerable to sleep disturbances associated with treatments, monitoring alarms, and care they receive. We hypothesiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25619b9dd76aef801d7d172875c21771
https://doi.org/10.1093/sleep/zsaa056.870
https://doi.org/10.1093/sleep/zsaa056.870