Zobrazeno 1 - 10
of 366
pro vyhledávání: '"D. Szczesniak"'
Autor:
L. Phillipson, M. Hevink, C. McAiney, M. Gresham, E. Conway, M. Mackowiak, D. Szczesniak, L. Smith, H. Brodaty, L. F. Low
Publikováno v:
International Journal of Qualitative Methods, Vol 22 (2023)
Research involving people with dementia has highlighted the need to improve engagement in the conduct of interviews and focus groups. Projective and enabling techniques may be useful and avoid some of the drawbacks associated with direct questioning.
Externí odkaz:
https://doaj.org/article/7f202e3c63654bb2b6fda6b5978a5341
Autor:
Don Hayes Jr., Rajni Kant Shukla, Yizi Cheng, Emrah Gecili, Marlena R. Merling, Rhonda D. Szczesniak, Assem G. Ziady, Jason C. Woods, Luanne Hall-Stoodley, Namal P.M. Liyanage, Richard T. Robinson
Publikováno v:
JCI Insight, Vol 7, Iss 12 (2022)
Nontuberculous mycobacteria (NTM) are an increasingly common cause of respiratory infection in people with cystic fibrosis (PwCF). Relative to those with no history of NTM infection (CF-NTMNEG), PwCF and a history of NTM infection (CF-NTMPOS) are mor
Externí odkaz:
https://doaj.org/article/4eb2e4ec73f04f1db4ca8742c6cfb12c
Autor:
Rhonda D. Szczesniak, Teresa Pestian, Leo L. Duan, Dan Li, Sophia Stamper, Brycen Ferrara, Elizabeth Kramer, John P. Clancy, Daniel Grossoehme
Publikováno v:
BMC Pulmonary Medicine, Vol 20, Iss 1, Pp 1-14 (2020)
Abstract Background Beginning at a young age, children with cystic fibrosis (CF) embark on demanding care regimens that pose challenges to parents. We examined the extent to which clinical, demographic and psychosocial features inform patterns of adh
Externí odkaz:
https://doaj.org/article/64285904fcbd4352b0c8c4c4b6c7d316
Autor:
Emrah Gecili, Cole Brokamp, Erika Rasnick, Pedro M. Afonso, Eleni‐Rosalina Andrinopoulou, Judith W. Dexheimer, John P. Clancy, Ruth H. Keogh, Yizhao Ni, Anushka Palipana, Teresa Pestian, Andrew Vancil, Grace C. Zhou, Weiji Su, Christopher Siracusa, Patrick Ryan, Rhonda D. Szczesniak
Publikováno v:
Pediatric Pulmonology, 58(5), 1501-1513. Wiley-Liss Inc.
Background: The extent to which environmental exposures and community characteristics of the built environment collectively predict rapid lung function decline, during adolescence and early adulthood in cystic fibrosis (CF), has not been examined. Ob
Publikováno v:
IEEE Journal of Translational Engineering in Health and Medicine, Vol 7, Pp 1-8 (2019)
The clinical course of cystic fibrosis (CF) lung disease is marked by acute drops of lung function, defined clinically as rapid decline. As such, lung function is monitored routinely through pulmonary function testing, producing hundreds of measureme
Externí odkaz:
https://doaj.org/article/112006e62b0a439fb46bb46aa8b151aa
Publikováno v:
PLoS ONE, Vol 16, Iss 1, p e0244173 (2021)
The novel coronavirus (COVID-19) is an emergent disease that initially had no historical data to guide scientists on predicting/ forecasting its global or national impact over time. The ability to predict the progress of this pandemic has been crucia
Externí odkaz:
https://doaj.org/article/3397070a5a534d12bd300910df82e226
Seasonality, mediation and comparison (SMAC) methods to identify influences on lung function decline
Autor:
Emrah Gecili, Anushka Palipana, Cole Brokamp, Rui Huang, Eleni-Rosalina Andrinopoulou, Teresa Pestian, Erika Rasnick, Ruth H. Keogh, Yizhao Ni, John P. Clancy, Patrick Ryan, Rhonda D. Szczesniak
Publikováno v:
MethodsX, Vol 8, Iss , Pp 101313- (2021)
This study develops a comprehensive method to assess seasonal influences on a longitudinal marker and compare estimates between cohorts. The method extends existing approaches by (i) combining a sine-cosine model of seasonality with a specialized cov
Externí odkaz:
https://doaj.org/article/18b93bdee9c949028ed4c9b86d184a64
Autor:
Karla Diaz-Ordaz, Rebecca Cosgriff, Gary Connett, Maarten van Smeden, Keith G. Brownlee, Emily Granger, Clemence Leyrat, Eleni-Rosalina Andrinopoulou, Rhonda D. Szczesniak, Nicholas P. Jewell, Ruth H. Keogh, Siobhán B. Carr, Daniela K Schlüter, Alex Lewin
Publikováno v:
Thorax
Thorax, 77(9), 873-881. BMJ Publishing Group
Thorax, 77(9), 873-881. BMJ Publishing Group
Background: cystic fibrosis (CF) is a life-threatening genetic disease, affecting around 10 500 people in the UK. Precision medicines have been developed to treat specific CF-gene mutations. The newest, elexacaftor/tezacaftor/ivacaftor (ELEX/TEZ/IVA)
Publikováno v:
Journal of Diabetes Research, Vol 2020 (2020)
Background. Characterizing maternal glucose sampling over the course of the entire pregnancy is an important step toward improvement in prediction of adverse birth outcome, such as preterm birth, for women with type 1 diabetes mellitus (T1DM). Object
Externí odkaz:
https://doaj.org/article/a26beb8fa7c744e2ba2432dbb697282c
Autor:
Benjamin D. Wissel, Hansel M. Greiner, Tracy A. Glauser, Francesco T. Mangano, Katherine D. Holland‐Bouley, Nanhua Zhang, Rhonda D. Szczesniak, Daniel Santel, John P. Pestian, Judith W. Dexheimer
Publikováno v:
Epilepsia.