Zobrazeno 1 - 10
of 157
pro vyhledávání: '"CF, Cystic fibrosis"'
Autor:
Federica Porcaro, Renato Cutrera
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Externí odkaz:
https://doaj.org/article/e0377ebb64cd412f9af778c6955a0c3d
Autor:
Szymczak Angelika, Ksiazek Piotr, Mojsym-Korybska Sylwia, Skorupa Wojciech, Zbikowska-Machul Albertyna
Publikováno v:
Current Issues in Pharmacy and Medical Sciences, Vol 31, Iss 4, Pp 200-203 (2018)
Cystic fibrosis is one of the most common genetic diseases among Caucasians due to its prevalence. Modern methods of molecular diagnostics and treatment of the disease allow to prolong the life of patients. In order to apply the appropriate treatment
Externí odkaz:
https://doaj.org/article/44b7b7dec984467dae0c085ea62c5457
Autor:
Nurlan Dauletbaev, Zoe S. Oftring, Wided Akik, Lukas Michaelis-Braun, Julia Korel, Larry C. Lands, Susanne Waldmann, Beate S. Müller, Michael Dreher, Gernot Rohde, Claus F. Vogelmeier, Sebastian Kuhn
Publikováno v:
Paediatric Respiratory Reviews
Mobile (m) Health technology is well-suited for Remote Patient Monitoring (RPM) in a patient's habitual environment. In recent years there have been fast-paced developments in mHealth-enabled pediatric RPM, especially during the COVID-19 pandemic, ne
Akademický článek
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Publikováno v:
JAAD Case Reports, Vol 18, Iss, Pp 71-73 (2021)
JAAD Case Reports
JAAD Case Reports
Autor:
George M. Solomon, Julianna Bailey, James Lawlor, Peter Scalia, Gregory S. Sawicki, Christopher Dowd, Kathryn A. Sabadosa, Aricca Van Citters
Publikováno v:
Journal of Cystic Fibrosis
Background During the COVID-19 pandemic, CF centers shifted to a telehealth delivery model. Our study aimed to determine how people with CF (PwCF) and their families experienced telehealth and assessed its quality and acceptability for future CF care
Autor:
Dana Albon, Aricca D. Van Citters, Thida Ong, Olivia Dieni, Christopher Dowd, Anne Willis, Kathryn A. Sabadosa, Peter Scalia, Kimberly Reno, Gabriela R. Oates, Michael S. Schechter
Publikováno v:
Journal of Cystic Fibrosis
Background Due to the COVID-19 pandemic, there was an uptake of telehealth in cystic fibrosis care. Previous studies show disparities in telehealth use based on socioeconomic status (SES). We aimed to: (1) understand telehealth use and perceptions an
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology
Cellular and Molecular Gastroenterology and Hepatology, Vol 12, Iss 5, Pp 1517-1529 (2021)
Cellular and Molecular Gastroenterology and Hepatology, Vol 12, Iss 5, Pp 1517-1529 (2021)
Background & Aims Autosomal recessive polycystic kidney disease (ARPKD) is caused by mutations in PKHD1, encoding fibrocystin/polyductin (FPC). Severe disease occurs in perinates. Those who survive the neonatal period face a myriad of comorbidities,
Publikováno v:
Acta Pharmaceutica Sinica B, Vol 11, Iss 6, Pp 1412-1433 (2021)
Acta Pharmaceutica Sinica. B
Acta Pharmaceutica Sinica. B
Anoctamin 1 (ANO1) or TMEM16A gene encodes a member of Ca2+ activated Cl– channels (CaCCs) that are critical for physiological functions, such as epithelial secretion, smooth muscle contraction and sensory signal transduction. The attraction and in
Akademický článek
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