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期刊名:European respiratory review

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ISSN:0905-9180

e-ISSN:1600-0617

IF/分区:10.8/Q1

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共收录本刊相关文章索引1476
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Valentina Tonazzo,Raimondo Junior Castaldo,Stefania Zanconato et al. Valentina Tonazzo et al.
Childhood interstitial lung disease (chILD) is a heterogeneous group of rare lung diseases that comprises more than 200 entities. The diagnostic process for chILD might require multiple investigations, which often include a combination of c...
Heather Girouard,Farah Jaber,Josh Gharib et al. Heather Girouard et al.
Elexacaftor-tezacaftor-ivacaftor (ETI) is a highly effective modulator therapy associated with significant improvements in respiratory function and quality of life among people living with cystic fibrosis (CF). However, ETI has also been sh...
Benjamin Griffiths,Reem Alajmi,Ian J Clifton et al. Benjamin Griffiths et al.
Background: Physical inactivity is a common and potentially modifiable trait in individuals with chronic airways disease, yet disease-specific physical activity profiles and clinical determinants remain poorly defined. ...
Christian Magnus Kragh Thomsen,Simon Kromann-Thomsen,Signe Thim et al. Christian Magnus Kragh Thomsen et al.
Background: Paediatric noncystic fibrosis bronchiectasis (NCFB) is a chronic respiratory condition characterised by airway infection, chronic inflammation, mucociliary dysfunction and structural lung damage. Emerging evid...
Wade Michaelchuk,Lesley J J Soril,Dacia Chiarieri-Hirsch et al. Wade Michaelchuk et al.
The rising global prevalence of post-COVID-19 condition (PCC) underscores the substantial and ongoing burden faced by individuals following severe acute respiratory syndrome coronavirus 2 infection. The volume of emerging evidence regarding...
Marc Peters-Golden,Sean M Fortier Marc Peters-Golden
The human and economic impact of idiopathic pulmonary fibrosis and other interstitial lung diseases is enormous, and available therapies are of limited utility. A decade after the introduction of the first antifibrotic agents, two new agent...
Annalisa Villa,Sébastien Sanges,Vincent Sobanski et al. Annalisa Villa et al.
Pulmonary arterial hypertension (PAH) is a severe disease characterised by a progressive thickening and obliteration of pulmonary vessels, resulting in increased vascular resistance, elevated pulmonary artery pressures, and right heart fail...
Prince Ntiamoah,Felix Wireko,Ajay Wagh et al. Prince Ntiamoah et al.
The bronchoscopic approach to diagnosing sarcoidosis has evolved significantly with the advent of advanced endoscopic and imaging-guided modalities. Bronchoscopy remains the cornerstone for both histological confirmation and therapeutic int...
Amro Hajja,Miral Atout,Rasoul Turko et al. Amro Hajja et al.
Background: Pleural malignancies pose a significant clinical challenge due to their poor prognosis and limited treatment options. Hyperthermic intrathoracic chemotherapy (HITHOC) is an emerging modality that has shown pro...
Thomas Radtke,Hà Pham-Ngoc,Thong Hua-Huy et al. Thomas Radtke et al.
Objective: This scoping review aims to map the available studies on single-breath pulmonary diffusing capacity for nitric oxide (D LNO) in various clinical diseases and identify gaps for future research. ...