The Delhi High Court has directed the central government to establish a national fund for rare diseases, ensuring effective treatment and monitoring for patients suffering from conditions like ...

The play is known as the Jackson Special. Kelly Maynard, Jackson’s mom, said he was diagnosed with Duchenne’s Muscular Dystrophy when he was five years old, which has confined him to a wheelchair. The ...

In a big homecoming night win, Hilliard Davidson's biggest play may have been a Jackson Maynard touchdown that didn't show up ...

I’d hoped we had time because he’s the youngest and still walking. We’d tried so hard to buy him that time, to slow down the disease progression so that he’d have skills to save, like upper body ...

Capricor Therapeutics (NASDAQ:CAPR) stock rallied 20% Friday afternoon following news the company plans to present long-term ...

The Delhi High Court on Friday directed the Union Government to constitute a “national rare diseases fund” and ordered ...

Melanie Sanford fought to get her son Hudson a breakthrough gene therapy to stop the progression of the fatal disease ...

SAN DIEGO, Oct. 04, 2024 (GLOBE NEWSWIRE) -- (NASDAQ: CAPR), a biotechnology company developing transformative cell and ...

Precision medicine offers tailored treatments for rare diseases, addressing genetic variations and improving therapeutic ...

A ‘Relive the 80s’ theme marked the occasion, which brought together 740 members of the commercial property industry at the ...

Avidity Biosciences excels in antibody oligonucleotide conjugates with its stock tripling in the past year due to innovative ...

Discover six innovative clinical-stage biotech companies fostering R&D in the Duchenne muscular dystrophy therapeutic space.