Results 1 to 10 of about 706,830 (273)
Pirfenidone and nintedanib are antifibrotic medications approved for idiopathic pulmonary fibrosis treatment by regulatory agencies and available for clinical use worldwide.
F. Amati +6 more
semanticscholar +1 more source
Connective tissue disease-associated interstitial lung disease (CTD-ILD) is a collection of systemic autoimmune disorders resulting in lung interstitial abnormalities or lung fibrosis.
G. Cerro Chiang, T. Parimon
semanticscholar +1 more source
Characterization of the PF-ILD phenotype in patients with advanced pulmonary sarcoidosis
Background Advanced pulmonary sarcoidosis causes significant morbidity and can lead to death. Large trials demonstrated efficacy of antifibrotics in patients with progressive fibrosing interstitial lung diseases (PF-ILD), including a few with sarcoidosis.
M. C. Schimmelpennink +7 more
doaj +1 more source
Decreased Survival and Lung Function in Progressive Pulmonary Fibrosis
Background and Objectives: Progressive pulmonary fibrosis (PPF) is a recently described term reserved for patients with fibrotic ILD other than idiopathic pulmonary fibrosis (IPF) with fast clinical deterioration. Here, survival and prognostic biomarkers
Mark G. J. P. Platenburg +3 more
doaj +1 more source
To analyze the efficacy and safety of nintedanib in patients with fibrosing autoimmune disease–related interstitial lung diseases (ILDs) with a progressive phenotype.
E. Matteson +14 more
semanticscholar +1 more source
No effect of danazol treatment in patients with advanced idiopathic pulmonary fibrosis
Background Telomere dysfunction can underly the development of idiopathic pulmonary fibrosis (IPF), and recent work suggests that patients with telomere syndromes might benefit from treatment with androgens, such as danazol.
Thijs W. Hoffman +4 more
doaj +1 more source
Background In patients with interstitial lung diseases (ILD), histopathological input is often required to obtain a diagnosis. Surgical lung biopsy (SLB) is considered the reference standard, but many patients are clinically unfit to undergo this ...
D. Korevaar +17 more
semanticscholar +1 more source
Clustering of lung diseases in the family of interstitial lung disease patients
Background The presence of familial interstitial lung disease (ILD) has been found to predict development of progressive pulmonary fibrosis. However, the role of non-ILD lung diseases in ILD patients’ families has not yet been investigated.
Michelle Terwiel +2 more
doaj +1 more source
Etiologic Classification of Diffuse Parenchymal (Interstitial) Lung Diseases
Interstitial lung diseases (ILD) or diffuse parenchymal lung diseases (DPLD) comprise a large number of disorders. Disease definition and classification allow advanced and personalized judgements on clinical disease, risks for genetic or environmental ...
M. Griese
semanticscholar +1 more source
Role of JAK/STAT in Interstitial Lung Diseases; Molecular and Cellular Mechanisms
Interstitial lung diseases (ILDs) comprise different fibrotic lung disorders characterized by cellular proliferation, interstitial inflammation, and fibrosis.
P. Montero +3 more
semanticscholar +1 more source

