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Thorax, ISSN 0040-6376, 12/2017, Volume 72, Issue Suppl 3, p. A109
IntroductionIdiopathic pulmonary fibrosis (IPF) is the most common form of interstitial lung disease, with a poor prognosis and a lack of therapeutic options... 
Pulmonary fibrosis
Journal Article
Thorax, ISSN 0040-6376, 12/2017, Volume 72, Issue Suppl 3, p. A24
Introduction and ObjectivesCough can be a debilitating symptom of idiopathic pulmonary fibrosis (IPF). The efficacy and safety of inhaled PA101, a novel... 
Pulmonary fibrosis
Journal Article
Thorax, ISSN 0040-6376, 12/2017, Volume 72, Issue Suppl 3, p. A250
Introduction and ObjectivesNintedanib and pirfenidone are licensed anti-fibrotic therapies (AFT) for the treatment of Idiopathic Pulmonary Fibrosis (IPF).1... 
Pulmonary fibrosis
Journal Article
Thorax, ISSN 0040-6376, 12/2017, Volume 72, Issue Suppl 3, p. A253
BackgroundSafety data on combined pirfenidone and nintedanib use are limited.MethodsA single-arm, open-label study (NCT02598193) assessed safety and... 
Pulmonary fibrosis
Journal Article
by K Deng and Z Liang and F Long and L Zhou and W Wu and M Chen and S Huang and D Cui and Y Gao and M Jiang and T Peng and Q Luo and R Chen
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 01/2017, Volume 195
Spearman's rank correlation matrix and unbiased classification were applied to explore the associations of autoantibodies profiles between serum and sputum.... 
Pulmonary fibrosis
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 01/2017, Volume 195
The baseline characteristics were: 36 (72%) males, mean (standard deviation (SD)) age 75 (7) years, Body Mass Index (BMI) 26.9 (4.6)kg/m2, Forced Vital... 
Pulmonary fibrosis
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 01/2017, Volume 195
Introduction: Current concepts of idiopathic pulmonary fibrosis (IPF) are that alveolar (ALV) epithelial injury leads to alternatively activated (M2)... 
Pulmonary fibrosis
Journal Article
by S Ikeda and A Sekine and T Baba and H Yamakawa and T Oda and R Okuda and H Kitamura and T Ogura
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 01/2017, Volume 195
Corresponding author's email: isatoshi0112@gmail.com [RATIONALE] After commercialization of nintedanib for idiopathic pulmonary fibrosis (IPF) in Japan, a high... 
Pulmonary fibrosis
Journal Article
by K Deng and Z Liang and F Long and L Zhou and W Wu and M Chen and S Huang and D Cui and Y Gao and M Jiang and T Peng and Q Luo and R Chen
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 01/2017, Volume 195
Serum and sputum supernatant samples obtained from IPF patients were interacted with the bead-antigen complex to detect the immunoglobulin G (IgG) antibodies... 
Pulmonary fibrosis
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 01/2017, Volume 195
Rationale: Idiopathic pulmonary fibrosis (IPF) is an unpredictable lung disease characterized by a progressive loss of lung function. For both % predicted FVC... 
Pulmonary fibrosis
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 01/2017, Volume 195
Familial and sporadic forms of IPF have been found to be strongly associated with the gain-of-function MUC5B promoter variant rs35705950, and in patients with... 
Pulmonary fibrosis
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 01/2017, Volume 195
Corresponding author's email: jonathan.galli2@tuhs.temple.edu Rationale: The clinical efficacy of antifibrotic agents in idiopathic pulmonary fibrosis (IPF)... 
Pulmonary fibrosis
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 01/2017, Volume 195
RATIONALE Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease associated with lung tissue scarring. CONCLUSION This model mimics the progressive... 
Pulmonary fibrosis
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 01/2017, Volume 195
The remaining patients carried diagnoses of either chronic hypersensitivity pneumonitis, NSIP, connective tissue disease related ILD, or dermatomyositis. With... 
Pulmonary fibrosis
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 01/2017, Volume 195
[...]it is unknown whether the efficacy were the same in the real world. [...]we assessed the clinical effect of nintedanib. Blood tests, high-resolution... 
Pulmonary fibrosis
Journal Article
ARTHRITIS & RHEUMATOLOGY, ISSN 2326-5191, 04/2019, Volume 71, Issue 4, pp. 652 - 653
Journal Article
Respiratory Medicine, ISSN 0954-6111, 03/2019, Volume 149, p. 42
Journal Article
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