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pro vyhledávání: '"Simon Hilldrup"'
Publikováno v:
Open Journal of Respiratory Diseases. 10:59-74
Idiopathic Pulmonary Fibrosis (IPF) is a chronic, progressive and life-limiting condition of unknown cause with no curative treatment. The impact of IPF on a patient’s quality of life is devastating and palliative treatment such as pulmonary rehabi
Autor:
Benjamin D. M. Hope-Gill, Simon Hilldrup, Russell P. Newton, Nicholas K. Harrison, Christine Davies
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 168:995-1002
Little is known about the pathogenesis of cough in idiopathic pulmonary fibrosis (IPF). We hypothesized that abnormalities of respiratory tract tachykinin-containing sensory nerves may be implicated. We studied cough response to capsaicin, substance
Publikováno v:
Cough (London, England)
Background: Patients with idiopathic pulmonary fibrosis (IPF) frequently develop a dry, irritating cough which often proves refractory to anti-tussive therapies. The precise pathogenetic mechanisms responsible for this cough are unknown. We hypothesi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e95b237afda596ac4945d690ed413c49