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期刊名:Clinical medicine insights-circulatory respiratory and pulmonary medicine

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ISSN:1179-5484

e-ISSN:1179-5484

IF/分区:0.9/Q4

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共收录本刊相关文章索引143
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
Hiroshi Furukawa,Shomi Oka,Kota Shimada et al. Hiroshi Furukawa et al.
Objective: Acute-onset diffuse interstitial lung disease (AoDILD) includes acute exacerbation of interstitial lung disease (ILD), drug-induced ILD, and Pneumocystis pneumonia in collagen diseases patients. As AoDILD cause...
Canna J Ghia,Raja Dhar,Parvaiz A Koul et al. Canna J Ghia et al.
Background: Streptococcus pneumoniae is one of the primary cause of community-acquired pneumonia (CAP) worldwide. However, scant data are available on the prevalence of etiological organisms for CAP in adolescent and adul...
Canna J Ghia,Raja Dhar,Parvaiz A Koul et al. Canna J Ghia et al.
Background: Streptococcus pneumoniae is one of the primary cause of community-acquired pneumonia (CAP) worldwide. However, scant data are available on the prevalence of etiological organisms for CAP in adolescent and adul...
Vasileios Kouritas,Richard Milton,Emmanouel Kefaloyannis et al. Vasileios Kouritas et al.
Background: The emphysema interventional treatment involves mainly lung volume reduction surgery (LVRS) and endobronchial valve (EBV) implantation. Few institutes discuss these cases at a dedicated emphysema multidiscipli...
Rebecca Keyte,Helen Egan,Michail Mantzios Rebecca Keyte
Risky behaviours are prevalent within the cystic fibrosis (CF) population; however, there is a lack of research which has investigated risky behaviour engagement among adolescents with CF, with reasons for initiation currently being unknown...
Emanuele Delfino,Filippo Del Puente,Federica Briano et al. Emanuele Delfino et al.
Clinical manifestations of respiratory fungal diseases in adult cystic fibrosis (CF) patients are very heterogeneous, ranging from asymptomatic colonization to chronic infections, allergic disorders, or invasive diseases in immunosuppressed...
Elizabeth Claire Elson,Joel Mermis,Deepika Polineni et al. Elizabeth Claire Elson et al.
Patients with cystic fibrosis (CF) develop pulmonary disease secondary to airway infection and dysregulated inflammation. Therapeutic innovations such as nebulized antimicrobial therapy targeting specific pathogens have resulted in improvem...
Alexander L Bisch,Courtney M Wheatley,Sarah E Baker et al. Alexander L Bisch et al.
Background: Cystic fibrosis (CF) is a genetic disease affecting multiple organ systems of the body and is characterized by mutation in the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR). Pr...
Anastasia Y Ipatova,Pamela H Koerner,Richard T Miller et al. Anastasia Y Ipatova et al.
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive lung disease which results in thickening and scarring of the interstitial tissue. As the only 2 Food and Drug Administration (FDA)-approved medications on the market, it is valua...
Dirk Habedank,Christian Opitz,Tim Karhausen et al. Dirk Habedank et al.
We hypothesized that the slope of relation ventilation to carbon dioxide output (V'E/V'CO2-slope) could be predictive already during the very first days after submassive pulmonary embolism (PE) to right ventricular systolic pressure (RVsys ...