A child with a rare genetic disease that affects mitochondria is the first person to receive a new experimental treatment for ...

The value of a recent biochemical discovery can be seen in the case of an 8-year-old boy who was playing typical sports in ...

Microglia replacement therapy helps treat people with a rare genetic condition called ALSP, suggesting the approach could ...

An 8-year-old boy, wheelchair-bound due to a rare genetic disease, HPDL deficiency, regained his mobility through an ...

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is a progressive neurological disease with an ...

Hudson Institute's leadership in RNA research has again been recognised, this time with a significant research grant from the Victorian government.Dr ...

Opioids accounted for 86 percent of all drug overdose deaths in the state with the highest overdose mortality rate.

For those who haven’t entered the valley of middle age, a CAC is a specialized CT scan that looks for calcium deposits in the ...

Among members of the Richardson family who carry a mutation in the PSEN1 gene, the average age when symptoms start is 39.

The death is the first recorded case of fatal pneumonic plague in the county since 2007, when a resident became infected after contact with a dead animal.

Chinese scientists have developed a novel nanotherapy known as biomimetic extracellular vesicle spherical nucleic acids ...

The World Heath Organisation has warned people of a 'fatal disease' being spread by mosquitoes in two neighbourhoods in Spain ...