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期刊名:Pulmonary medicine

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ISSN:2090-1836

e-ISSN:2090-1844

IF/分区:2.1/Q3

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共收录本刊相关文章索引264
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
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Rokhsara Rafii,Timothy E Albertson,Samuel Louie et al. Rokhsara Rafii et al.
Chronic obstructive pulmonary disease (COPD) is a debilitating pulmonary disorder with systemic effects, and it is the fourth leading cause of death in the United States. COPD patients not only develop respiratory limitations, but can also ...
J J Egan,H I Adamali,S S Lok et al. J J Egan et al.
Hypothesis. Repeated epithelial cell injury secondary to viruses such as Epstein Barr and subsequent dysfunctional repair may be central to the pathogenesis of IPF. In this observational study, we evaluated whether a combination of standard...
Nidhi Sood,Nikhil Sood,Vibhu Dhawan Nidhi Sood
Pulmonary arteriovenous malformations (PAVMs), although most commonly congenital, are usually detected later in life. We present a case of a 25-year-old woman with no previous history of AVM or telangiectasia, who presented with life-threat...
Scott Burgess,Peter Sly,Sunalene Devadason Scott Burgess
Suboptimal adherence with preventive medication is common and often unrecognised as a cause of poor asthma control. A number of risk factors for nonadherence have emerged from well-conducted studies. Unfortunately, patient report a physicia...
Mark J Hamblin,Maureen R Horton Mark J Hamblin
Interstitial lung disease (ILD) is an increasingly recognized complication of rheumatoid arthritis (RA) contributing to significantly increased morbidity and mortality. Diagnosis can be challenging since patients are unlikely to report dysp...
Erica P A Rutten,Thomas B Grydeland,Sreekumar G Pillai et al. Erica P A Rutten et al.
The objective of the present study was to determine the association between CT phenotypes-emphysema by low attenuation area and bronchitis by airway wall thickness-and body composition parameters in a large cohort of subjects with and witho...
Atsushi Watanabe,Nobuyoshi Kawaharada,Tetsuya Higami Atsushi Watanabe
Idiopathic pulmonary fibrosis (IPF) is characterized by slowly progressive respiratory dysfunction. Nevertheless, some IPF patients experience acute exacerbations generally characterized by suddenly worsening and fatal respiratory failure w...
Masahito Ebina,Hiroyuki Taniguchi,Taku Miyasho et al. Masahito Ebina et al.
The pathogenesis of acute exacerbation of idiopathic pulmonary fibrosis (IPF) remains to be elucidated. To evaluate the roles of inflammatory mediators in acute exacerbation, the concentrations of high mobility group protein B1 (HMGB1), a c...
Mike Althaus,Wolfgang G Clauss,Martin Fronius Mike Althaus
The development of pulmonary edema can be considered as a combination of alveolar flooding via increased fluid filtration, impaired alveolar-capillary barrier integrity, and disturbed resolution due to decreased alveolar fluid clearance. An...
Shu Hisata,Yuichiro Kimura,Naoko Shibata et al. Shu Hisata et al.
Both SP-D and KL-6/MUC1 are established biomarkers of the interstitial pneumonias, including idiopathic pulmonary fibrosis (IPF), but the causes and clinical outcomes based on their independent effects are not known. Eleven asymptomatic pat...