A spokesperson for the developer said a £4.7 million contract of works is starting this week, which will remedy the problems ...

New Gene Therapy Approach Shows Promise for Duchenne Muscular Dystrophy July 24, 2024 — Researchers have made a significant breakthrough in developing a new gene therapy approach that restores ...

2025 will be a very eventful year for BridgeBio. In addition to the commercial launches of Attruby in the United States, ...

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Maintaining a regular walking routine offers a wealth of health benefits for individuals across all age groups. From young adults to seniors, incorporating daily walks can enhance cardiovascular ...

which is lacking in individuals with a less common form of the disease known as limb girdle muscular dystrophy type 2B/R2. There are more than 30 types of muscular dystrophies, all of which weaken ...

A small trial of an experimental vaccine has shown promising results for patients with the most aggressive type of breast ...

Facioscapulohumeral muscular dystrophy (FSHD) is a rare genetic muscle disease that affects the muscles ... Most children with FSHD remain able to walk. FSHD is caused by certain gene changes ...

Regenxbio reported Monday the first clinical evidence showing improved muscle function in boys with Duchenne muscular dystrophy following treatment with its experimental gene therapy. The positive ...