Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Benjamin D Hope-Gill"'
Publikováno v:
PLoS ONE, Vol 12, Iss 11, p e0187847 (2017)
Dry cough is a common symptom described in patients with Idiopathic Pulmonary Fibrosis (IPF) and impairs quality of life. The exact mechanisms causing cough in IPF remain unclear, however evidence suggests altered cough neurophysiology and sensitisat
Externí odkaz:
https://doaj.org/article/bc78d8171381456998a466d0a2195fcd
Autor:
Jeremy P.T. Ward, Christopher Corrigan, Beth Mansfield, Kasope L. Wolffs, Petar A. Popov, Daniel A. Pass, Daniela Riccardi, Richard T. Bruce, Paul J. Kemp, Benjamin D. Hope-Gill
Publikováno v:
Molecular pathology and functional genomics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a25390669f0c36649e21cd719c7a720e
https://doi.org/10.1183/13993003.congress-2021.pa669
https://doi.org/10.1183/13993003.congress-2021.pa669
Autor:
Richard Attanoos, Bethan Mansfield, Christopher Corrigan, Jeremy P.T. Ward, Benjamin D. Hope-Gill, Dirk Adriaensen, Richard T. Bruce, R Paes De Araújo, Luis A. J. Mur, Line Verckist, Kasope L. Wolffs, Daniela Riccardi, Paul J. Kemp
Publikováno v:
Modelling lung disease in vitro/vivo.
Introduction Idiopathic pulmonary fibrosis (IPF) is a disease with very poor prognosis and no curative therapies. The extracellular calcium-sensing receptor (CaSR) is a chemosensor which is activated by several agonists/modulators including polyvalen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::094c83283d097b93b2622116168da4f8
https://doi.org/10.1136/thorax-2019-btsabstracts2019.98
https://doi.org/10.1136/thorax-2019-btsabstracts2019.98
Publikováno v:
Future directions of hospice care: IPU or ITU?.
Background Idiopathic Pulmonary Fibrosis (IPF) is a progressive condition of the lung with no known cause or cure. Whilst treatments slow disease progression, symptom control remains paramount to improving quality of life. Cough is a predominant symp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5a5b6c5f9b97a7b487b76e6fe5776cb
https://doi.org/10.1136/spcare-2019-mariecuriepalliativecare.32
https://doi.org/10.1136/spcare-2019-mariecuriepalliativecare.32
Autor:
Benjamin D. Hope-Gill, Annmarie Nelson, Catherine Sampson, Anthony Byrne, Nicholas K. Harrison
Publikováno v:
BMJ Supportive & Palliative Care. 5:113.2-113
Introduction Idiopathic pulmonary fibrosis (IPF) is a chronic, fibrotic interstitial lung disease of unknown origin and median survival of three years. National Institute for Clinical Excellence guidelines promote patient and carer centred approaches
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8834126bc649b4a445fe804ebd9b6203
https://doi.org/10.1136/bmjspcare-2014-000838.30
https://doi.org/10.1136/bmjspcare-2014-000838.30