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Category Archives: Muscular Dystrophy Treatment

Govt to fund gene therapy research on NCDs, rare diseases – CNBCTV18

Posted: Published on November 21st, 2019

The central government has decided to support research on gene therapy in a big way to tackle Indias escalating burden of non-communicable diseases (NCDs) and inherited critical disorders such as spinal muscular atrophy (SMA), thalassemia and haemophilia. Scientific institutions and universities conducting research on genomics and its therapeutic applications will soon get a financial fillip from public coffers, under an initiative facilitated and funded by the Indian Council of Medical Research (ICMR). Gene therapy is a technique that uses genetic modifications to treat or prevent diseases. Continue reading

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Vamorolone Designated Promising Innovative Medicine (PIM) for Treatment of Duchenne Muscular Dystrophy by the UK MHRA – BioSpace

Posted: Published on October 28th, 2019

Pratteln, Switzerland, October 21, 2019 Santhera Pharmaceuticals (SIX: SANN) announces that the UKs Medicines and Healthcare Products Regulatory Agency (MHRA) has informed ReveraGen BioPharma about having designated vamorolone as Promising Innovative Medicine (PIM) for the treatment of Duchenne muscular dystrophy (DMD). We congratulate ReveraGen on this success and are excited about the PIM designation as it further validates the potential of vamorolone as an innovative treatment approach addressing the high unmet medical need in young patients with DMD, said Thomas Meier, PhD, CEO of Santhera Continue reading

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Duchenne Muscular Dystrophy Treatment Market 2019 Delivering Valuable Insights on Business Statistics, Growth Factors by Top Key Players, and Regions…

Posted: Published on October 28th, 2019

The Duchenne Muscular Dystrophy Treatment Market research report 2019 has been estimated considering the application and regional segments, market share, and size, while the forecast for each product type and application segment has been provided for the global and regional markets. Duchenne Muscular Dystrophy Treatment report offers detailed profiles of the key players to bring out a clear view of the competitive landscape of the Duchenne Muscular Dystrophy Treatment outlook. It also comprehends market new product analysis, financial overview, strategies and marketing trends Continue reading

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Adjusting to Life Without My Gallbladder – Muscular Dystrophy News

Posted: Published on October 28th, 2019

Thats right. Youll be able to resume your regular diet after gallbladder removal. My surgeons words ring in my ears as my television airs food commercials and I chomp on carrot sticks. Continue reading

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Parent Project Muscular Dystrophy Awards $148000 in Grants to Nationwide Children’s Hospital and University of Missouri to Improve Cardiac Function in…

Posted: Published on October 28th, 2019

HACKENSACK, N.J., Oct. Continue reading

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Hes a part of us: North senior is the heart of the Wildcats – WQAD Moline

Posted: Published on October 28th, 2019

Please enable Javascript to watch this video DAVENPORT, Iowa -- The Davenport North Wildcats are on the verge of a historic season. "We know one more loss and we're done for the year." said North Head Coach, Adam Hite Continue reading

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Stories from the Heart: Adaptive Halloween costumes for kids with disabilities – PIX11 New York

Posted: Published on October 28th, 2019

Please enable Javascript to watch this video GARMENT DISTRICT Halloween is a time of joy for children. But for many parents who have children with disabilities, finding a costume that fits the needs of their child can be difficult. That is until now, as lots of kids are getting a treat this year! They're wearing Target adaptive costumes for those with disabilities Continue reading

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Positive Early Results Support Continuation of Phase 2 Trial of ATL1102 for DMD – Muscular Dystrophy News

Posted: Published on October 17th, 2019

Experimental therapy ATL1102 improved upper limb strength and function in six boys with Duchenne muscular dystrophy (DMD) unable to walk, according to early results of an ongoing Phase 2 clinical trial. Continue reading

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Living with a neuromuscular disease – KELOLAND.com

Posted: Published on October 17th, 2019

Neuromuscular diseases are rare, however, the number of people who have them in South Dakota is larger than many small towns in the state. Thats why the Muscular Dystrophy Association is working to bring cures and treatments to those individuals. It needs your support in order to help families like the Van Overbekes Continue reading

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Wishing well | Make-A-Wish Foundation partners with Hall’s RV to gift terminally ill child new camper – Sand Mountain Reporter

Posted: Published on October 17th, 2019

Enjoying the great outdoors in style will be a little easier for Levi Bryant thanks to the Make-A-Wish Foundation and Halls RV in Albertville. Being a 6-year-old thats terminally ill has made things difficult for Levi. He lives in Attalla with his parents, Neil and Ashley Bryant and his older brother Caleb Continue reading

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