Zobrazeno 1 - 10
of 113
pro vyhledávání: '"Sonya L Heltshe"'
Autor:
Mitchell J Brittnacher, Sonya L Heltshe, Hillary S Hayden, Matthew C Radey, Eli J Weiss, Christopher J Damman, Timothy L Zisman, David L Suskind, Samuel I Miller
Publikováno v:
PLoS ONE, Vol 11, Iss 7, p e0158897 (2016)
Comparative analysis of gut microbiomes in clinical studies of human diseases typically rely on identification and quantification of species or genes. In addition to exploring specific functional characteristics of the microbiome and potential signif
Externí odkaz:
https://doaj.org/article/6236252a04b94dc4aa9e175f7ae957c7
Autor:
David P. Nichols, Sarah J. Morgan, Michelle Skalland, Anh T. Vo, Jill M. Van Dalfsen, Sachinkumar B.P. Singh, Wendy Ni, Lucas R. Hoffman, Kailee McGeer, Sonya L. Heltshe, John P. Clancy, Steven M. Rowe, Peter Jorth, Pradeep K. Singh, the PROMISE-Micro Study Group
Publikováno v:
The Journal of Clinical Investigation, Vol 133, Iss 10 (2023)
Background Lung infections are among the most consequential manifestations of cystic fibrosis (CF) and are associated with reduced lung function and shortened survival. Drugs called CF transmembrane conductance regulator (CFTR) modulators improve act
Externí odkaz:
https://doaj.org/article/f38c402d2a6340749497b7d56e6094d6
Autor:
Alexander Eng, Hillary S. Hayden, Christopher E. Pope, Mitchell J. Brittnacher, Anh T. Vo, Eli J. Weiss, Kyle R. Hager, Daniel H. Leung, Sonya L. Heltshe, Daniel Raftery, Samuel I. Miller, Lucas R. Hoffman, Elhanan Borenstein
Publikováno v:
BMC Microbiology, Vol 21, Iss 1, Pp 1-17 (2021)
Abstract Background Infants with cystic fibrosis (CF) suffer from gastrointestinal (GI) complications, including pancreatic insufficiency and intestinal inflammation, which have been associated with impaired nutrition and growth. Recent evidence iden
Externí odkaz:
https://doaj.org/article/69900369972c4aafab8be30c1ed91e63
Autor:
Sarah Jane Schwarzenberg, Phuong T. Vu, Michelle Skalland, Lucas R. Hoffman, Christopher Pope, Daniel Gelfond, Michael R. Narkewicz, David P. Nichols, Sonya L. Heltshe, Scott H. Donaldson, Carla A. Frederick, Andrea Kelly, Jessica E. Pittman, Felix Ratjen, Margaret Rosenfeld, Scott D. Sagel, George M. Solomon, Michael S. Stalvey, John P. Clancy, Steven M. Rowe, Steven D. Freedman
Publikováno v:
Journal of Cystic Fibrosis. 22:282-289
Elexacaftor/tezacaftor/ivacaftor (ETI) improves pulmonary disease in people with cystic fibrosis (PwCF), but its effect on gastrointestinal symptoms, which also affect quality of life, is not clear.PROMISE is a 56-center prospective, observational st
Autor:
Baha Moshiree, A. Jay Freeman, Phuong T. Vu, Umer Khan, Carmen Ufret-Vincenty, Sonya L. Heltshe, Christopher H. Goss, Sarah Jane Schwarzenberg, Steven D. Freedman, Drucy Borowitz, Meghana Sathe
Publikováno v:
Journal of Cystic Fibrosis. 22:266-274
People with cystic fibrosis (PwCF) suffer from gastrointestinal (GI) symptoms affecting their quality of life (QOL). Despite the relevance of GI symptoms to the overall health of PwCF, a paucity of studies only have comprehensively assessed the preva
Autor:
A Jay, Freeman, Rong, Huang, Sonya L, Heltshe, Daniel, Gelfond, Daniel H, Leung, Bonnie R, Ramsey, Drucy, Borowitz, Meghana, Sathe
Publikováno v:
J Cyst Fibros
BACKGROUND: Concerns related to stool consistency are common in the first year of life among children with cystic fibrosis (CF). However, normal stool patterns for infants with CF have not been described. METHODS: Secondary analysis was completed fro
Autor:
J. Kirk Harris, Brandie D. Wagner, Charles E. Robertson, Mark J. Stevens, Conor Lingard, Drucy Borowitz, Daniel H. Leung, Sonya L. Heltshe, Bonnie W. Ramsey, Edith T. Zemanick
Publikováno v:
Journal of Cystic Fibrosis.
Autor:
M. Skalland, Christopher H. Goss, Patrick A. Flume, Natalie E. West, Umer Khan, Sonya L. Heltshe, Donald R. VanDevanter, Don B. Sanders
Publikováno v:
J Cyst Fibros
BACKGROUND: In the STOP2 (Standardized Treatment of Pulmonary Exacerbations-2) study, intravenous (IV) antimicrobial treatment duration for adults with cystic fibrosis (CF) experiencing pulmonary exacerbations (PEx) was determined based on initial tr
Publikováno v:
Journal of Cystic Fibrosis.
Autor:
Sonya L. Heltshe, Umer Khan, Alex C Paynter, Christopher H. Goss, Nicole Hamblett, Noah Lechtzin
Publikováno v:
Journal of Cystic Fibrosis. 21:78-83
Background The COVID-19 pandemic has accelerated the transition to telehealth, including the use of home spirometry in cystic fibrosis. Evaluating the accuracy and precision of longitudinal home spirometry is a requisite for telehealth-based research