Results 11 to 20 of about 445,273 (266)
Comorbidities in interstitial lung diseases
European Respiratory Review, 2017 Fibrosing lung disorders include a large number of diseases with diverse behaviour. Patients can die because of the progression of their illness, remain stable or even improve after appropriate treatment has been instituted.
George A. Margaritopoulos +2 more
doaj +1 more source
Journal of Obstetrics and Gynaecology, 2004 Interstitial cystitis (IC) is a debilitating chronic inflammatory disorder of the bladder. It affects predominantly middle-aged Caucasian women. The diagnosis, made from the combination of symptoms, cystoscopic findings and bladder biopsies, is often delayed in the gynaecology setting because of a low index of suspicion.
D O, Selo-Ojeme, J L, Onwude
openaire +2 more sources
International Brazilian Journal of Urology, 2009 Purpose: We evaluated the effectiveness of combining behavioral therapy, pharmacologic therapy and endoscopic hydrodistension for treating painful bladder syndrome / interstitial cystitis (PBS/IC).
Robert S. Hanley +4 more
doaj +1 more source
Overnight desaturation in interstitial lung diseases: links to pulmonary vasculopathy and mortality
ERJ Open ResearchBackground Overnight desaturation predicts poor prognosis across interstitial lung diseases (ILDs). The aim of the present study was to investigate whether nocturnal desaturation is associated with pulmonary vasculopathy and mortality.
George A. Margaritopoulos +13 more
doaj +1 more source
Respiratory Research, 2023 Introduction Interstitial lung disease (ILD) may be difficult to distinguish from other respiratory diseases due to overlapping clinical presentation. Recognition of ILD is often late, causing delay which has been associated with worse clinical outcome ...
Iris G. van der Sar +6 more
doaj +1 more source
Erasmus Syndrome—A Rare Cause of Diffuse Cutaneous Systemic Sclerosis due to Silica Exposure: A Case Report [PDF]
Bengal Physician JournalErasmus syndrome is a rare disease characterized by the development of systemic sclerosis (SSc) in the background of silica exposure or silicosis. Here we report a case of a 42-year-old male who presented with skin tightening for 2 years and progressive ...
Shankar Dey +5 more
doaj +1 more source
Cryptogenic Organizing Pneumonia: Evolution of Morphological Patterns Assessed by HRCT
Diagnostics, 2020 To evaluate the radiological findings in patients with cryptogenic organizing pneumonia (COP) before steroid treatment and their behavior after therapy, we retrospectively evaluated a total of 22 patients with a diagnosis of COP made by bronchoalveolar ...
Francesco Tiralongo +13 more
doaj +1 more source
Predictors and changes of physical activity in idiopathic pulmonary fibrosis
BMC Pulmonary Medicine, 2022 Background Different clinical predictors of physical activity (PA) have been described in idiopathic pulmonary fibrosis (IPF), but studies are lacking evaluating the potential role of muscle strength and anxiety and depression symptoms in PA limitation ...
Diana Badenes-Bonet +15 more
doaj +1 more source
Evolving Concepts in Progressive Pulmonary Fibrosis: A Clinical Update
Journal of RespirationProgressive pulmonary fibrosis (PPF) is a clinical syndrome associated with worsening quality of life and increased mortality among patients with various interstitial lung diseases.
María Belén Noboa-Sevilla +8 more
doaj +1 more source