Results 61 to 70 of about 5,660 (245)
Respirology, Volume 29, Issue 12, Page 1023-1046, December 2024.Abstract Hypersensitivity pneumonitis (HP) is an immune‐mediated interstitial lung disease (ILD) relating to specific occupational, environmental or medication exposures. Disease behaviour is influenced by the nature of exposure and the host response, with varying degrees of lung inflammation and fibrosis seen within individuals. The differentiation of
Hayley Barnes +15 more
wiley +1 more source
Incidence, Prevalence, and Survival of Patients with Idiopathic Pulmonary Fibrosis in the UK. [PDF]
, 2018 INTRODUCTION: Recent developments in the care of patients with idiopathic pulmonary fibrosis have the potential to improve survival rates. Population-based estimates of the current disease burden are needed to evaluate the future impact of newly approved
Kausar, Imran +2 more
core +3 more sources
Multidisciplinary Respiratory Medicine, 2013 BackgroundTh-2 cytokine milieu including interleukin 4 (IL-4) was detected in fibrotic lung diseases. Chronic extrinsic allergic alveolitis (EAA) may be also accompanied by marked fibrogenesis.
M. Sterclova +4 more
semanticscholar +1 more source
Journal of Medical Virology, Volume 96, Issue 7, July 2024.Abstract Donor and recipient human cytomegalovirus (HCMV) seropositive (D+R+) lung transplant recipients (LTRs) often harbor multiple strains of HCMV, likely due to transmitted donor (D) strains and reactivated recipient (R) strains. To date, the extent and timely occurrence of each likely source in shaping the post‐transplantation (post‐Tx) strain ...
Büsra Külekci +9 more
wiley +1 more source
Autoimmune Hypothyroidism As a Predictor of Mortality in Chronic Hypersensitivity Pneumonitis
Frontiers in Medicine, 2017 BackgroundChronic hypersensitivity pneumonitis (CHP) is a fibrotic parenchymal lung disease that occurs when inhalation of environmental antigens leads to immune dysregulation.
Ayodeji Adegunsoye +9 more
doaj +1 more source
Fibrotic lung diseases in children
Pediatric Pulmonology, Volume 59, Issue 5, Page 1165-1174, May 2024.Abstract In children, pulmonary fibrosis (PF) is an extremely unusual entity that can be observed in some types of interstitial lung disease (ILD). Defining whether ILD is accompanied by PF is important for targeted therapy. Algorithm for the diagnosis of PF in children is not clearly established.
Birce Sunman, Nural Kiper
wiley +1 more source
PAS staining of bronchoalveolar lavage cells for differential diagnosis of interstital lung disease
Diagnostic Pathology, 2009 Bronchoalveolar lavage (BAL) is a useful diagnostic tool in interstitial lunge diseases (ILD). However, differential cell counts are often non specific and immunocytochemistry is time consuming.
Zabel Peter, Hauber Hans P
doaj +1 more source
Effects of bioaerosol exposure on work-related symptoms among Swiss sawmill workers [PDF]
, 2018 Objective: Exposure to bioaerosols in the occupational environment of sawmills could be associated with a wide range of health effects, in particular respiratory impairment, allergy and organic dust toxic syndrome.
Charrière, N. +3 more
core
Journal of Medical Primatology, Volume 53, Issue 1, February 2024.Abstract In recent times, global viral outbreaks and diseases, such as COVID‐19 (SARS‐CoV‐2), Zika (ZIKV), monkeypox (MPOX), Ebola (EBOV), and Marburg (MARV), have been extensively documented. Swiftly deciphering the mechanisms underlying disease pathogenesis and devising vaccines or therapeutic interventions to curtail these outbreaks stand as ...
Taeho Kwon
wiley +1 more source
Interstitial lung disease in Malta [PDF]
, 2012 Aim: To establish the prevalence, management and response to treatment of interstitial lung disease (ILD) in Malta. Methodology: The personal files of 102 living and 26 deceased patients with ILD under the care of 4 respiratory physicians were reviewed ...
Fenech, Manwel +2 more
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