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Autor:
Antonios Charokopos, Jay H. Ryu, Effrosyni D. Manali, Vasilios Tzilas, Spyridon Papiris, Lykourgos Kolilekas, Demosthenes Bouros
Publikováno v:
Chest. 161:748-752
Publikováno v:
Chest. 158:1350-1360
Background The functional consequence of airway obstruction in asthma can be regionally measured using inhaled gas MRI. Ventilation defects visualized by MRI persist post-bronchodilator in patients with severe asthma with uncontrolled sputum eosinoph
Autor:
Diana Ernst, Hendrik Suhling, Marius M. Hoeper, Jan B. Hinrichs, Tobias Welte, Jan-Christopher Kamp, Bernd Schönhofer, Danny Jonigk
Publikováno v:
Chest. 158:e127-e132
Case presentation A 37-year-old previously healthy and athletic woman presented to the ED in October 2018 with acute-onset high fever, dyspnea, and productive cough. Chest radiograph showed bilateral infiltrates that correlated with multifocal ground
Publikováno v:
Chest. 158:901-912
Background Nonadherence to oral prednisolone is an important driver of poor control in severe asthma, and its detection is warranted to guide management. Research Question The goal of this study was to evaluate the utility of liquid chromatography an
Autor:
Sean B. Fain
Publikováno v:
Chest. 158:1293-1295
Autor:
Martin Jenkins, Nicolas Roche, Paul Dorinsky, Samuel Israel, Ezanul Abd Wahab, Magnus Aurivillius, Roopa Trivedi, Omar S. Usmani
Publikováno v:
Chest. 158:A2435-A2437
Publikováno v:
Chest. 158:e89-e91
Bronchiolitis obliterans syndrome (BOS) after allogeneic hematopoietic cell transplantation (allo-HCT) usually confers poor prognosis and high mortality. Currently, therapeutic options are limited. Here we report an 18-year-old man with acute myeloid
Publikováno v:
J Cardiol Cases
A wild-type ATTR amyloidosis is a systemic disease with multi-organ dysfunction, involving heart, kidney, skin, and gastrointestinal tract, due to deposition of wild-type transthyretin in each organ. We had a 76-year-old man diagnosed with wild-type
Publikováno v:
Chest
Publikováno v:
Chest. 154:e89-e92
Idiopathic pulmonary fibrosis is the most common idiopathic interstitial pneumonia. Prognosis is poor with a median survival