Results 51 to 60 of about 3,166 (214)
Telomerase modRNA Offers a Novel RNA‐Based Approach to Treat Human Pulmonary Fibrosis
Recombinant linear and circular hTERT mRNA restore telomerase activity in primary ATII cells and ex vivo lung tissue from patients with pulmonary fibrosis, leading to telomere elongation, reduced DNA damage, and decreased senescence and fibrosis markers.
Jia Li Ye +14 more
wiley +1 more source
Several lines of research indirectly suggest that platelet activating factor (PAF) may intervene in the pathogenesis of extrinsic allergic alveolitis (EAA).
J-L. Pérez-Arellano +5 more
doaj +1 more source
Comorbidities and survival in patients with chronic hypersensitivity pneumonitis
Introduction Chronic Hypersensitivity Pneumonitis (cHP) is a fibrotic interstitial lung disease (ILD) resulting from repeated exposure to an offending antigen.
Julia Wälscher +6 more
doaj +1 more source
Acute life-threatening extrinsic allergic alveolitis in a paint controller [PDF]
Background Occupational diisocyanate-induced extrinsic allergic alveolitis (EAA) is a rare and probably underestimated diagnosis. Two acute occupational EAA cases have been described in this context, but neither of them concerned hexamethylene ...
Bieler, G. +6 more
core
Respiratory Ill‐Health and Welding Exposures: A Canadian Cohort Study
ABSTRACT Introduction Respiratory ill‐health in welders is well documented but without a clear indication of exposures responsible. Methods In a Canadian cohort study of welders and electrical workers, we collected self‐reports of asthma/wheeze and rhinitis at each 6‐monthly contact for up to 5 years.
Jean‐Michel Galarneau +2 more
wiley +1 more source
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]
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
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
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
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

