The 33-year-old took to Instagram on Friday (January 24) to address a slew of false rumors. First, she hit back at a claim that Child Protective Services had to check in on her daughter, who she ...
On a cold night outside the Ritz 26 years ago today, the Royal Family changed for ever as the Prince of Wales and Camilla ...
Johnny Quintana’s life changed at the age of 19 when he was diagnosed with a rare form of muscular dystrophy called ...
While the last decade has brought considerable progress for patients with DMD, substantial unmet need remains. Several ...
Active duty military troops have arrived in San Diego after President Trump's order to secure the border. An electric ...
The gene therapy improved motor functions in children with Duchenne muscular dystrophy two years after treatment ...
Teen Mom star Leah Messer admits it’s “very challenging” helping daughter Aliannah “balance” her desire for freedom with the ...
Sidra Medicine, a member of Qatar Foundation, has established a gene therapy centre to treat rare genetic diseases such as ...
The Muscular Dystrophy Association (MDA) proudly announces the launch of its 75th anniversary campaign, marking a legacy of progress in research, care, ...
The data showed reduced difficulties in standing, walking and running that were statistically significant, the company said.
Scholar Rock submitted its BLA of apitegromab for the treatment of patients with Spinal Muscular Atrophy with a request for Priority Review to be given. Explore more details here.