News-Medical.Net on MSN
Smartphones match traditional methods in monitoring patients with muscular dystrophy
Stanford Medicine researchers found that a smartphone could monitor patients with two types of muscular dystrophy as well as ...
This novel therapy offers the first FDA-approved option to address the root cause of this ultra-rare condition, which causes progressive muscle weakness impairing walking, breathing, and swallowing.
Sarepta said on Monday that its late-stage study testing two gene-targeted therapies for Duchenne muscular dystrophy did not ...
His parents Stephen and Jenny have asked Sheffield Children's NHS Foundation Trust to approve the use of drug givinostat, ...
An 11-year-old girl with muscular dystrophy was given a cheer as she walked down the hallway of Southampton Hospital as part ...
If a boy in New York has been convinced to think he’s a girl, the state Medicaid program has got you covered. But if a boy ...
InvestorsHub on MSN
BridgeBio stock soars after breakthrough Phase 3 data for muscular dystrophy treatment
BridgeBio Pharma (NASDAQ:BBIO) shares surged 15% on Monday after the company announced highly positive Phase 3 results for ...
Researchers from Leiden University Medical Center and the University of Florida have found hundreds of blood proteins in ...
SCHENECTADY, N.Y. — A father of two sons diagnosed with muscular dystrophy is organizing a cornhole tournament this weekend to raise money for research and awareness of the condition. Stephen Gilbert, ...
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