Send Us your News and/or Sports Tip:

Mutations in the MECP2 gene, which lead to most cases of Rett syndrome, prevent the formation of droplet-like structures that regulate DNA.

A new report, released yesterday by the Australian Institute for Health and Welfare (AIHW) confirms how widespread mental illness...

Duchenne muscular dystrophy (DMD) is a rapidly progressive form of muscular dystrophy caused by a mutation in the DMD gene.

I’ve known for a long time that I have anxiety.

The Committee for Orphan Medicinal Products, a branch of the European Medicines Agency (EMA).

Dylan Alcott says he doesn't know if he would "even be here at all" if it were not for the impact sport has had on his life.

Dr Dinesh Palipana had struggled to maintain employment that was otherwise guaranteed to medical graduates because of a spinal cord injury.

Levels of inflammatory markers in the lungs may help predict pulmonary exacerbations in children with cystic fibrosis (CF).

Tofersen, Biogen’s investigational therapy for people with familial amyotrophic lateral sclerosis (ALS) caused by SOD1 gene mutations.

Record numbers of early childhood education and care (ECEC) professionals, along with educators in other fields of education.

Treatment with Tysabri (natalizumab) can lessen disability in people with relapsing-remitting multiple sclerosis (RRMS).

Some survivors of acute bouts of Covid-19 experience a range of persistent medical issues — some lasting for weeks, or even months...

About a year ago, my sister and I went to an arts and crafts store. Upon entering, I instinctively wanted to steer the shopping cart, and of

An FDA-approved diabetes drug shows early signs of promise against the most common genetic form of amyotrophic lateral sclerosis.

The JobTrainer program aims to assist school leavers and job seekers with learning new skills in target areas identified by the National Sk

New technology could enable faster and more accurate cystic fibrosis (CF) diagnoses by non-invasively tracking the movement of air through

Hansa Biopharma has granted an exclusive worldwide license to Sarepta Therapeutics to develop and promote imlifidase as a gene therapy pre-

By targeting a protein called BRD4, an experimental cancer treatment known as JQ1 reversed cellular abnormalities and extended survival in

Hansa Biopharma has granted an exclusive worldwide license to Sarepta Therapeutics to develop and promote imlifidase as a gene therapy pre-

An experimental drug for a rare, inherited form of amyotrophic lateral sclerosis (ALS) has shown promise in phase 1/2 clinical trials, ...