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5130 results for "lung disease"
A world-first inhaled RNA therapy that targets the root cause of lung disease has entered human trials in Australia. The breakthrough could transform treatment for nine million Australians living with chronic lung conditions.
Scientists are developing better treatments for idiopathic pulmonary fibrosis, a deadly lung disease that kills most patients within five years. Understanding the genetic and environmental causes is finally leading to hope for the 3 million people affected worldwide.
Scientists discovered a genetic link that could finally explain why some people develop a deadly lung disease. A breakthrough drug tested in mice offers hope for millions living with idiopathic pulmonary fibrosis.
A treatment for a rare bacterial lung infection just proved it can help patients much sooner than before. The drug, already approved for advanced cases, now shows real benefits when given to newly diagnosed patients.
Yankees legend Bernie Williams lost his father to a lung disease that took five years to diagnose. Now he's helping others recognize the warning signs that could save lives.
Two companies are teaming up to manufacture medicines in orbit, where zero gravity could create more effective treatments for people with rare lung diseases. The first missions launch in 2026, bridging decades of space research with real patient benefits.
Japan has approved a groundbreaking new treatment for two deadly lung diseases, offering hope to thousands of patients who've had limited options for over ten years. The drug slows lung function decline and could transform how doctors treat these life-threatening conditions.
A simple questionnaire developed in India is revolutionizing how doctors diagnose a deadly lung condition that has long stumped medical professionals. The tool achieves over 90% accuracy and could save countless lives across South Asia.
A new AI tool can predict serious lung problems in premature babies just by analyzing routine eye exam photos. The breakthrough could help doctors catch and treat breathing issues earlier, potentially saving tiny lives.
Scientists found a molecular switch that tells lung cells whether to repair damage or fight infection. The discovery could lead to new treatments for chronic lung diseases like COPD and pulmonary fibrosis.
A woman's lung nearly doubled in size after cancer surgery, proving organs scientists thought were fixed can actually regenerate. The discovery could reverse incurable diseases affecting millions worldwide.
Researchers discovered how a protein called vitronectin triggers deadly lung scarring, opening the door to new treatments for a disease that currently has no cure. The breakthrough could help thousands living with pulmonary fibrosis breathe easier.
A breakthrough study from Sweden shows that giving extremely premature babies early hydrocortisone treatment dramatically increases their chances of surviving without lifelong lung disease. The simple, safe treatment could help thousands of the tiniest patients worldwide.
Researchers are unlocking new ways to detect and treat lung cancer in people who've never smoked, a distinct form of the disease that's often caught too late. Countries like Taiwan are already testing screening programs for at-risk non-smokers, offering hope for earlier detection.
A groundbreaking injection just got approved for NHS use in England and Wales, offering fresh hope to 30,000 people struggling with severe COPD. This marks the first biologic therapy available for uncontrolled chronic lung disease after years of limited innovation.
Crown Princess Mette-Marit of Norway successfully received a new lung at Oslo University Hospital, offering hope after an eight-year battle with a rare lung disease. The 52-year-old royal is recovering well under close medical supervision.
Northwestern Medicine doctors are saving lives by offering lung transplants to stage 4 cancer patients whose disease hasn't spread beyond their lungs. All 17 transplant patients survived their first year, compared to grim outcomes for those on standard treatment alone.
A groundbreaking treatment for Huntington's disease just cleared a major hurdle, bringing hope to 240,000 Americans affected by this devastating condition. The experimental therapy could become the first disease-modifying treatment for a disorder that has had none.
A groundbreaking treatment for myotonic dystrophy type 1 reduced toxic proteins by 40% and improved muscle function in patients who've never had disease-modifying options. The New England Journal of Medicine just published results that could lead to the first approved therapy for this progressive, often fatal disease.
Researchers discovered how to disguise healthy mitochondria so they can slip into diseased cells undetected, extending the lives of mice with a fatal genetic disorder. The breakthrough could one day help children born with rare mitochondrial diseases.
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