Muscular Dystrophy

Genetic Mutation Could Worsen Heart Function in Duchenne Muscular Dystrophy Patients – Newswise

  A mutation in the gene that…

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What I Learned About Life From My Dog – Muscular Dystrophy News

Me and Gus on the day we took him home. (Photos by…

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Telehealth ‘Helpful’ Alternative to In-person Care, Rare Disease Patients Say – Muscular Dystrophy News

A majority of rare disease patients using telehealth during the COVID-19 pandemic thought the experience…

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New Documentary Follows Family After Sons’ Muscular Dystrophy Diagnosis – The Mighty

What happened: A rare form of muscular dystrophy is chronicled in a new documentary where…

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FDA approves new drug to treat common form of muscular dystrophy based on research from U of A scientist – Folio

The U.S. FDA has approved a drug called viltolarsen to treat Duchenne…

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Removing Barriers to Employment for People With Disabilities – Muscular Dystrophy News

  As a journalist and person with Duchenne…

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New Drug Could Offer Hope for Muscular Dystrophy Patients – Technology Networks

A new drug offers hope for young boys with the progressive neuromuscular disease Duchenne muscular…

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New Duchenne muscular dystrophy drug shows benefit in clinical trial – Medical Xpress

  A new drug offers hope for young boys…

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Muscular Dystrophy and Other Clinical Trials Adapting to Life With COVID-19 – Muscular Dystrophy News

In a Facebook Live event hosted by the Muscular Dystrophy Association (MDA), experts discussed the…

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Potential treatment strategy found for muscular dystrophy – Medical News Today

  DMD is…

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Scientists uncover a novel approach to treating Duchenne muscular dystrophy – Sanford Burnham Prebys

The study reveals a promising new therapeutic approach for the incurable muscle-wasting condition. Scientists at Sanford…

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Scientists uncover a novel approach to treating Duchenne muscular dystrophy – EurekAlert

As Duchenne muscular dystrophy progresses, levels of a beneficial RNA (purple), called…

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CRISPR gene-editing tool tweaked to tackle muscular dystrophy via RNA – New Atlas

Muscle fibers treated with a new RNA-targeted Cas9 technique show a lack…

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Drugging the undruggable: Yale finds treatment path for muscular dystrophy – Yale News

  Researchers at Yale have identified a possible treatment for Duchenne…

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Ocean deep, sky high: Man with muscular dystrophy challenges himself with extreme sports – CGTN

22-year-old Fang Jianze, who had been told by doctors that he would not be able…

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One year in, 9 boys with muscular dystrophy show remarkable progress from gene therapy – Genetic Literacy Project

Cheerful boy with muscular dystrophy sitting on playroom floor, looking towards the…

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I’m Sleeping Comfortably Now, Thanks to a New Mattress – Muscular Dystrophy News

  Most mitochondrial myopathy patients rely on sleep as…

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Losing My Ability to Walk Won’t Stop Me – Muscular Dystrophy News

  When I was younger, I couldn’t imagine…

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MD Advocates Offer Advice to Disabled Students During Pandemic – Muscular Dystrophy News

The importance of communication and self-care for people with muscular dystrophy and other neuromuscular diseases…

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Personal health budgets: Call for change to Wales’ care system – BBC News

Rhys Bowler says he would like the choice of who provides his…

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