Medical research

Scientists find rare disease clues in cell's recycling system

Scientists have demonstrated how an investigational drug works against a rare, fatal genetic disease, Niemann-Pick type C1 (NPC1). They found that a closely related compound will activate an enzyme, AMPK, triggering a cellular ...

Attention deficit disorders

Movement disorders in young people related to ADHD

Researchers at the University of Copenhagen and the Copenhagen University Hospital have identified a particular genetic mutation that may cause parkinsonism in young people. The mutation interferes with the brain's transport ...

Ophthalmology

Colour vision link may help myopia research

(Medical Xpress)—A possible link between colour vision and the development of myopia - or near-sightedness - has been discovered by an international group, including a researcher from The University of Western Australia.

Diseases, Conditions, Syndromes

A new way of looking at Prader-Willi Syndrome

An Australian study reveals that people with the rare genetic disorder known as Prader-Willi Syndrome may have an impaired autonomic nervous system. This discovery opens up a new way of looking at the insatiable appetite ...

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