Myotonic Dystrophy | NEJM
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YouTubeNEJM Group
Myotonic Dystrophy | NEJM
A. Normal inspection and handshake B. Percussion myotonia C. Grip-release myotonia
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Myotonic dystrophy
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Muscular Dystrophy - Causes, Types, Symptoms, Prognosis, Treatment
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What Is Myotonic Dystrophy? Understanding Muscle Weakness And Wasting.
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What Is Myotonic Dystrophy? Understanding Muscle Weakness And Wasting.
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Closing in on a cure for Duchenne muscular dystrophy | Brain | Discovery | UT Southwestern Medical Center
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utswmed.org
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3.1K views · 52 reactions | Happy #WorldScienceDay!  We're proud to fund groundbreaking research which aims to learn more about muscle wasting conditions and lead us to new treatments. This year, as part of our President's Awards, we were delighted to present Dr Ami Ketley with the Early Career Scientist Award. Dr Ketley is currently working towards treatment and symptoms for Myotonic Dystrophy. Learn more about our research: https://loom.ly/FkSJwGY | Muscular Dystrophy UK | Facebook
0:27
3.1K views · 52 reactions | Happy #WorldScienceDay!  We're proud to fund groundbreaking research which aims to learn more about muscle wasting conditions and lead us to new treatments. This year, as part of our President's Awards, we were delighted to present Dr Ami Ketley with the Early Career Scientist Award. Dr Ketley is currently working towards treatment and symptoms for Myotonic Dystrophy. Learn more about our research: https://loom.ly/FkSJwGY | Muscular Dystrophy UK | Facebook
FacebookMuscular Dystrophy UK
936 views4 weeks ago
How can an RNA be used to treat myotonic dystrophy? ARTHEx biotech is focused on the development of the next generation of RNA therapies for genetic diseases. Our first product in the pipeline is a first-in-class treatment against myotonic dystrophy type 1, an orphan and rare disease. This therapy is based on an antisense oligonucleotide that inhibits the action of microRNAs (also known as antimiR). Learn more now: | Sci Ani
2:00
How can an RNA be used to treat myotonic dystrophy? ARTHEx biotech is focused on the development of the next generation of RNA therapies for genetic diseases. Our first product in the pipeline is a first-in-class treatment against myotonic dystrophy type 1, an orphan and rare disease. This therapy is based on an antisense oligonucleotide that inhibits the action of microRNAs (also known as antimiR). Learn more now: | Sci Ani
FacebookSci Ani
5.4K viewsJul 5, 2021