Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Isabel P. Neuringer"'
Autor:
Bethany L. Bartley, Carolyn E. Schwartz, Roland B. Stark, Anna M. Georgiopoulos, Deborah Friedman, Christopher J. Richards, Henry L. Dorkin, T. Bernard Kinane, Isabel P. Neuringer, Lael M. Yonker
Publikováno v:
BMC Pulmonary Medicine, Vol 20, Iss 1, Pp 1-9 (2020)
Abstract Background Many individuals with cystic fibrosis (CF) die from respiratory failure without referral for lung transplant. Physician practices that may expedite, delay, or preclude referral, are poorly understood. Methods Two parallel, web-bas
Externí odkaz:
https://doaj.org/article/49bdb292fdce485abdd30764bd38a760
Autor:
Isabel P. Neuringer
Publikováno v:
Clinical and Developmental Immunology, Vol 2013 (2013)
Posttransplant lymphoproliferative disease (PTLD) after lung transplantation occurs due to immunosuppressant therapy which limits antiviral host immunity and permits Epstein-Barr viral (EBV) replication and transformation of B cells. Mechanistically,
Externí odkaz:
https://doaj.org/article/efe9dfc09eb0428db5f3d2f555f1577b
Publikováno v:
BMJ Open Quality, Vol 9, Iss 4 (2020)
Externí odkaz:
https://doaj.org/article/e563438063814854970e75dacd69d8fc
Autor:
Henry L. Dorkin, Lael M. Yonker, Christopher J. Richards, Bethany L. Bartley, Isabel P. Neuringer, Deborah Friedman, T. Bernard Kinane, Roland B. Stark, Carolyn E. Schwartz, Anna M. Georgiopoulos
Publikováno v:
BMC Pulmonary Medicine, Vol 20, Iss 1, Pp 1-9 (2020)
BMC pulmonary medicine, 20:58
BMC Pulmonary Medicine
BMC pulmonary medicine, 20:58
BMC Pulmonary Medicine
Background Many individuals with cystic fibrosis (CF) die from respiratory failure without referral for lung transplant. Physician practices that may expedite, delay, or preclude referral, are poorly understood. Methods Two parallel, web-based survey
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a133fe183a5b9d56de1d57222949f810
http://link.springer.com/article/10.1186/s12890-020-1067-4
http://link.springer.com/article/10.1186/s12890-020-1067-4
Autor:
Deborah J. Wexler, Kevin J. Scully, Leonard Sicilian, Melanie P. Ruazol, Gregory S. Sawicki, Lael M. Yonker, Melissa S. Putman, Ahmet Uluer, Jordan Sherwood, Mary E. Larkin, Hui Zheng, Peter Marchetti, Kimberly Martin, Isabel P. Neuringer
Publikováno v:
J Clin Endocrinol Metab
Context The clinical utility and implications of continuous glucose monitoring (CGM) in cystic fibrosis (CF) are unclear. Objective We examined the correlation between CGM measures and clinical outcomes in adults with CF, investigated the relationshi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36f755e9cadb9700421f80964acc187b
https://europepmc.org/articles/PMC8947309/
https://europepmc.org/articles/PMC8947309/
Autor:
Isabel P. Neuringer
Publikováno v:
The Journal of Heart and Lung Transplantation. 38:585-588
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0abbcf51ee0a0edffc832b423cf0fa25
https://doi.org/10.1016/j.healun.2019.01.008
https://doi.org/10.1016/j.healun.2019.01.008
Autor:
Michael Bruce, Catherine M. Gordon, Logan B Greenblatt, Leonard Sicilian, Taisha Joseph, Gregory S. Sawicki, Joel S. Finkelstein, Hang Lee, Melissa S. Putman, Ahmet Uluer, Mary L. Bouxsein, Isabel P. Neuringer
Publikováno v:
J Clin Endocrinol Metab
Context Cystic fibrosis (CF) transmembrane conductance (CFTR) dysfunction may play a role in CF-related bone disease (CFBD). Ivacaftor is a CFTR potentiator effective in improving pulmonary and nutritional outcomes in patients with the G551D-CFTR mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f1bedeb2a2225d0daba19ff27760e48
https://europepmc.org/articles/PMC7947772/
https://europepmc.org/articles/PMC7947772/
Publikováno v:
BMJ Open Quality, Vol 9, Iss 4 (2020)
BMJ Open Quality
BMJ Open Quality
Lung transplant is a potential life-lengthening option for individuals with cystic fibrosis (CF) and advanced lung disease. However, referral for transplant evaluation is not made for the majority of patients with CF with low lung function who die ea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84d16c58df8723e55edf438cedf8aead
https://bmjopenquality.bmj.com/content/9/4/e001031.full
https://bmjopenquality.bmj.com/content/9/4/e001031.full
Autor:
Denis Hadjiliadis, Baharak Moshiree, Sarah E. Hempstead, Albert Faro, Lianne G. Singer, Teresa Schindler, Peter H. Michelson, Joan Zukosky, Richard Simon, Lauren Vignola, E. Tallarico, Carl Riedy, Elisabeth P. Dellon, Siddhartha G. Kapnadak, Joseph M. Pilewski, Daniel U Gochenour, James Albright, Emily DiMango, Isabel P. Neuringer, Dave Young, Shaina Blair, Christian Benden
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 19(3)
Background Advanced cystic fibrosis lung disease (ACFLD) is common, is associated with reduced quality of life, and remains the most frequent cause of death in individuals with cystic fibrosis (CF). These consensus guidelines provide recommendations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3240342192839c5edc23fe0b8ee47faa
https://pubmed.ncbi.nlm.nih.gov/32115388
https://pubmed.ncbi.nlm.nih.gov/32115388
Autor:
Anita St. John, Samuel M. Moskowitz, Anna M. Georgiopoulos, Deborah Friedman, Leonard Sicilian, Rachel W. Linnemann, Lael M. Yonker, Allen Lapey, Isabel P. Neuringer, Suhayla Islam, M. Shannon Fracchia, Lily L. Altstein, Kieu-Tram Bach
Publikováno v:
Pediatric pulmonology. 54(7)
BACKGROUND Despite the significant impact of chronic symptoms on quality of life with cystic fibrosis (CF), the role of palliative care in management of this disease is not well defined. The coping, goal assessment, and relief from evolving CF sympto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffb05f5d0a7222875d336b354351666f
https://pubmed.ncbi.nlm.nih.gov/30854795
https://pubmed.ncbi.nlm.nih.gov/30854795