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Activation of the epithelial Na+ channel (ENaC) requires CFTR Cl- channel function

Autor: Paul M. Quinton, M. J. Light, M. M. Reddy

Publikováno v: Nature. 402:301-304

It is increasingly being recognized that cells coordinate the activity of separate ion channels that allow electrolytes into the cell. However, a perplexing problem in channel regulation has arisen in the fatal genetic disease cystic fibrosis, which

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::382d0d47e00d8e435ec55c838a9e1d3f
https://doi.org/10.1038/46297

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Supporting cystic fibrosis disease management during adolescence: the role of family and friends

Autor: D H, Barker, K A, Driscoll, A C, Modi, M J, Light, A L, Quittner

Publikováno v: Child: care, health and development. 38(4)

Successful management of a complex disease, such as cystic fibrosis (CF), requires support from family and friends; however, few studies have examined social support in adolescents with CF.Twenty-four adolescents were interviewed about the support th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::afceadaa0a0dcbf32187acabb6e0f522
https://pubmed.ncbi.nlm.nih.gov/21771002

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Epidemiologic study of cystic fibrosis: design and implementation of a prospective, multicenter, observational study of patients with cystic fibrosis in the U.S. and Canada

Autor: W J, Morgan, S M, Butler, C A, Johnson, A A, Colin, S C, FitzSimmons, D E, Geller, M W, Konstan, M J, Light, H R, Rabin, W E, Regelmann, D V, Schidlow, D C, Stokes, M E, Wohl, H, Kaplowitz, M M, Wyatt, S, Stryker

Publikováno v: Pediatric pulmonology. 28(4)

Cystic fibrosis (CF) is a complex illness characterized by chronic lung infection leading to deterioration in function and respiratory failure in over 85% of patients. An understanding of the risk factors for that progression and the interaction of t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6dc4cf0b06e16408cae2dd144c548fb9
https://pubmed.ncbi.nlm.nih.gov/10497371

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Allergic bronchopulmonary aspergillosis in cystic fibrosis: reported prevalence, regional distribution, and patient characteristics. Scientific Advisory Group, Investigators, and Coordinators of the Epidemiologic Study of Cystic Fibrosis

Autor: D E, Geller, H, Kaplowitz, M J, Light, A A, Colin

Publikováno v: Chest. 116(3)

Using the large database from the Epidemiologic Study of Cystic Fibrosis (ESCF), the objectives of this study were to (1) estimate the reported prevalence of allergic bronchopulmonary aspergillosis (ABPA) in patients with cystic fibrosis (CF); (2) co

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9aa6eab57b64fcd7a46a783a62368825
https://pubmed.ncbi.nlm.nih.gov/10492265

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The clinical utility of event recording

Autor: M J, Light, M S, Sheridan

Publikováno v: Caring : National Association for Home Care magazine. 9(12)

In summary, event recording is a cost-effective means of obtaining objective evidence about a baby's cardiorespiratory patterns at home. It is particularly useful in joint decisionmaking at the time of discharge if parents (or clinicians) remain anxi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::25a635d92a1a2ce2090d6d0c2c3b914c
https://pubmed.ncbi.nlm.nih.gov/10108599

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Home monitoring in Hawaii: the first 1,000 patients

Autor: M J, Light, M S, Sheridan

Publikováno v: Hawaii medical journal. 48(8)

By February 1988, 1,000 Hawaii infants had been prescribed cardiorespiratory monitors for use at home. By 1986, 12.3/1000 live births were being monitored, principally for apnea related to prematurity but also following Apparent Life Threatening Epis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::20a819948805356d218ee635afbb9230
https://pubmed.ncbi.nlm.nih.gov/2793451

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