News
10h
Irish Mirror on MSNDevastated mum urges Irish approval for lifechanging medicine for son with life-limiting conditionAlfie Ennis suffers from Duchenne muscular dystrophy and is in desperate need of medication to help his condition ...
7h
Dublin Live on MSNDevastated Dublin mum fights for life-changing medicine to be approved for sonArchie Ennis suffers from Duchenne muscular dystrophy and is in desperate need of medication to help his condition ...
2d
Amazon S3 on MSNJAR of Hope’s Manalapalooza raises funds for Duchenne muscular dystrophy researchJAR of Hope helps support a team of researchers and doctors who are aiming to eliminate Duchenne muscular dystrophy – a fatal ...
Tevard Biosciences, Inc., a privately held biotechnology company pioneering tRNA-based therapies to cure a broad range of ...
Avidity shares early del-brax FSHD data showing improved mobility, strength, and safety; Phase 3 FORWARD trial now underway.
Jesse’s Journey is well-known in London, and this gives me a chance to meet people who supported us back then and thank them ...
8d
MedPage Today on MSNCardiac Complications of Duchenne Muscular DystrophyCardiac complications in Duchenne muscular dystrophy (DMD) are the result of cardiac muscle involvement that accompanies the ...
Satellos Bioscience Chief Scientific Officer discusses early-stage trials of the company's Duchenne muscular dystrophy drug, ...
Regenxbio Inc.’s gene therapy in treating Duchenne muscular dystrophy (DMD) produced positive initial phase I/II results from ...
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