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Experts representing multiple societies and institutions across 14 countries have published guidance for computed tomography ...
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News-Medical.Net on MSNGlobal experts release guidance on CT imaging for post-COVID lung abnormalitiesExperts representing multiple societies and institutions across 14 countries have published guidance for computed tomography (CT) imaging in patients with residual lung abnormalities after COVID-19 ...
Experts representing multiple societies and institutions across 14 countries have published guidance for computed tomography (CT) imaging in patients with residual lung abnormalities after COVID-19 ...
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Irish Examiner on MSNElderly Cork man died after week-long delay in acting on X-ray showing swallowed denturesThe HSE has apologised to the family of an elderly man who died with choking complications after it took a hospital a week to act on an X-ray that showed he had swallowed his own dentures. The apology ...
Many lung cancers in nonsmokers have no known cause and are discovered only by chance.
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HealthDay on MSNConsensus Offers Best Practices for Post-COVID-19 Residual Abnormalities on Chest CTIn an international multisociety consensus statement, published online July 22 in Radiology, recommendations are presented for computed tomography (CT) imaging in patients with residual lung ...
Research shows that in patients presenting to the emergency department with acute dyspnea, increased calprotectin was associated with 90-day mortality.
If you’re having trouble breathing or sleeping, you’re not alone—and there’s help available. As a pulmonologist and sleep ...
No improvement in clinical outcomes occurred among inpatients with COVID-19 who received nirtmatrelvir-ritonavir or molnupiravir in addition to usual care.
The Parkinson’s Foundation recommends that in addition to making an appointment with an internist or family practitioner, a person experiencing symptoms should also see a movement disorders specialist ...
A 36-year-old woman with recurrent pneumothorax and no clear risk factors is found to have a rare inherited syndrome, diagnosed only through genetic testing.
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