Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Susan S. Li"'
Publikováno v:
Journal of Cystic Fibrosis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::388692e53d55e1602a6e9b07fca4786b
https://doi.org/10.1016/j.jcf.2023.03.014
https://doi.org/10.1016/j.jcf.2023.03.014
Autor:
Peter P. Stanich, Phil A. Hart, Georgios I. Papachristou, Yevgeniya Gokun, Luis F. Lara, Kyle Porter, Darwin L. Conwell, Somashekar G. Krishna, Michael R. Wellner, Stephen Kirkby, Mitchell L. Ramsey, Susan S Li, Lindsay A. Sobotka
Publikováno v:
Am J Gastroenterol
Introduction Acute pancreatitis (AP) occurs among patients with pancreas-sufficient cystic fibrosis (PS-CF) but is reportedly less common among patients with pancreas-insufficient cystic fibrosis (PI-CF). The incidence of AP may be influenced by cyst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09428f63d02b5ef44cec922d2f6d7df1
https://doi.org/10.14309/ajg.0000000000001527
https://doi.org/10.14309/ajg.0000000000001527
Autor:
Stephen Kirkby, Peter P. Stanich, Susan S Li, Michael P. Meara, Mitchell L. Ramsey, Alice Hinton, Darwin L. Conwell, Somashekar G. Krishna, Lindsay A. Sobotka
Publikováno v:
World Journal of Gastrointestinal Endoscopy
BACKGROUND Symptomatic biliary and gallbladder disorders are common in adults with cystic fibrosis (CF) and the prevalence may rise with increasing CF transmembrane conductance regulator modulator use. Cholecystectomy may be considered, but the outco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c899acb02e0f4cb70262239e185acc9
http://europepmc.org/articles/PMC8474692
http://europepmc.org/articles/PMC8474692
Autor:
Mitchell L. Ramsey, Susan S. Li, Luis F. Lara, Yevgeniya Gokun, Venkata S. Akshintala, Darwin L. Conwell, John Heintz, Stephen E. Kirkby, Karen S. McCoy, Georgios I. Papachristou, Alpa Patel, Vikesh K. Singh, Phil A. Hart
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
Cystic fibrosis transmembrane conductance regulator (CFTR) modulators improve pulmonary outcomes in subjects with cystic fibrosis (CF); however, the effects on pancreatic manifestations are not well characterized. We hypothesized that CFTR modulators
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39505095812155687e0a4c5d3fc1eb9f
https://pubmed.ncbi.nlm.nih.gov/36008229
https://pubmed.ncbi.nlm.nih.gov/36008229
Autor:
Mitchell L Ramsey, Michael R Wellner, Kyle Porter, Stephen E Kirkby, Susan S Li, Luis F Lara, Sean G Kelly, A James Hanje, Lindsay A Sobotka
Publikováno v:
World journal of hepatology. 14(2)
Cystic fibrosis transmembrane conductance regulator (CFTR) modulators significantly improve pulmonary function in patients with cystic fibrosis (CF) but the effect on hepatobiliary outcomes remains unknown. We hypothesized that CF patients on CFTR mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c579aaa10eb194daec9daad37521d79
https://pubmed.ncbi.nlm.nih.gov/35317183
https://pubmed.ncbi.nlm.nih.gov/35317183
Autor:
Don Hayes, Dmitry Tumin, William C. L. Stewart, Rebecca Miller, Joseph D. Tobias, Susan S. Li
Publikováno v:
Chest. 156:64-70
Background The lung allocation score (LAS) prioritizes lung transplant (LTx) candidates with poor transplant-free survival and expected survival benefit from LTx. Although patients with the highest LAS have the shortest waiting time, mortality benefi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6be3e6cb79ae626e856b6cf2346c8063
https://doi.org/10.1016/j.chest.2019.01.008
https://doi.org/10.1016/j.chest.2019.01.008
Autor:
Mitchell L. Ramsey, Cheryl E. Gariepy, Luis F. Lara, Susan S. Li, Stephen Kirkby, Phil A. Hart, Alice Hinton, Maisam Abu-El-Haija, Darwin L. Conwell, Somashekar G. Krishna
Publikováno v:
Pancreas. 50(5)
OBJECTIVES We hypothesized that hospitalizations in cystic fibrosis (CF) would reflect the development of age-related comorbidities. METHODS A retrospective analysis was performed using the Nationwide Inpatient Sample (2002-2017). Hospitalizations fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccc2ec28cfd5ca245daf4f5867c1df63
https://pubmed.ncbi.nlm.nih.gov/34016889
https://pubmed.ncbi.nlm.nih.gov/34016889
Publikováno v:
Annals of the American Thoracic Society
Rationale: Health insurance coverage has been implicated as a socioeconomic factor affecting clinical outcomes in patients with cystic fibrosis (CF), but evidence for this is mixed and varies by age.Objectives: Focusing on adolescents and young adult
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1141e12affa0c02d93de41e0de834278
https://pubmed.ncbi.nlm.nih.gov/33522873
https://pubmed.ncbi.nlm.nih.gov/33522873
Publikováno v:
Hospital Pediatrics. 7:692-696
An 8-year-old girl with neurofibromatosis type 1 and mild intermittent asthma presented with an 8-day history of a daily fever between 101°F and 105°F, a nonproductive cough, congestion, a sore throat, and myalgias, despite treatment with amoxicill
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f09a6cc75ebbb5f91fb89ec96486f2d
https://doi.org/10.1542/hpeds.2017-0071
https://doi.org/10.1542/hpeds.2017-0071
Autor:
Debra Boyer, Katie A. Krone, Don Hayes, Susan S. Li, Stephen Kirkby, Dmitry Tumin, Heidi M. Mansour
Publikováno v:
Expert review of respiratory medicine. 12(11)
Survival after lung transplantation lags behind outcomes of other solid organ transplants, and complications from lung transplant are the second most common cause of death in cystic fibrosis. Evolving surgical techniques, therapeutics, and perioperat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23b8a2c9fab597dc8b8f6b2a93a93cfe
https://pubmed.ncbi.nlm.nih.gov/30198350
https://pubmed.ncbi.nlm.nih.gov/30198350