Medical research

Tongue-on-a-chip provides insight into genetic diseases

Muscular dystrophy is a group of rare genetic diseases that cause progressive muscle weakness and deterioration. For decades, researchers have struggled to understand how the disease works and to find suitable treatments.

Neuroscience

Simple urine test for motor neurone disease

A researcher at Flinders University has developed a simple urine test that gives a quantitative measure of the severity of motor neurone disease.

Medications

FDA Oks first muscular dystrophy drug; awaits proof it works

Federal regulators on Monday granted tentative approval to the first drug for muscular dystrophy, following an intense public campaign from patients and doctors who pushed for the largely unproven medication.

Oncology & Cancer

New study supports surgery as treatment for myasthenia gravis

In a global study of myasthenia gravis, an autoimmune disease that causes muscle weakness and fatigue, researchers found that surgical removal of an organ called the thymus reduced patients' weakness, and their need for immunosuppressive ...

Pediatrics

The dying child: Room for improvement in end-of-life care

Many pediatricians and pediatric subspecialists believe that their clinical care extends from treating ill children through end-of-life care. However, are pediatricians actually meeting the needs of families and their dying ...

Medications

FDA delay raises slim hope for muscular dystrophy drug

Federal health regulators will take more time to review a highly-contested drug for muscular dystrophy that has become a flashpoint in the debate over patient access to experimental medicine.

Diseases, Conditions, Syndromes

Study strengthens suspected link between Zika and paralysis

A study in Brazil found nearly 90 percent of people with a rare paralyzing condition said they had symptoms of Zika earlier—contributing to mounting evidence that Zika may be a cause.

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