To find all the Tour Duchenne Muscular Dystrophy information you are interested in, please take a look at the links below.
End Duchenne Tour Recap: Memphis, TN - Parent Project ...
https://www.parentprojectmd.org/end-duchenne-tour-recap-memphis-tn/
Nov 04, 2019 · PPMD’s End Duchenne Tour made a stop in Memphis, TN on Saturday, October 26. We were joined by over 60 people, including families, an amazing group of volunteers in our kids room, six members of the Le Bonheur Children’s Hospital team, and …
FDA OKs Viltolarsen (Viltepso) for Duchenne Muscular Dystrophy
https://www.medscape.com/viewarticle/935624
"The FDA is committed to fostering drug development for serious neurological disorders like Duchenne muscular dystrophy," Billy Dunn, MD, director, Office of Neuroscience of the FDA's Center for ...
Duchenne Muscular Dystrophy: Symptoms, Diagnosis, and ...
https://www.webmd.com/children/duchenne-muscular-dystrophy
To learn more about Duchenne muscular dystrophy or find a support group in your area, visit: Cure Duchenne, the Muscular Dystrophy Association, or the Parent Project Muscular Dystrophy.
End Duchenne Tour - Parent Project Muscular Dystrophy
https://www.parentprojectmd.org/get-involved/attend-events/end-duchenne-tour/
End Duchenne Tour 2020: Virtual Tour Stop in Atlanta End Duchenne Tour 2020: Virtual Tour Stop in Atlanta On the morning of March 14, the Duchenne community in and around Atlanta, GA, gathered for PPMD’s first virtual End Duchenne Tour Stop of the year…. Learn More
'79 Challenge' brings awareness to Duchenne Muscular ...
https://kstp.com/minnesota-news/79-challenge-brings-awareness-to-duchenne-muscular-dystrophy/5849418/
2 days ago · 6-year-old Caleb and 5-year-old Duncan (Dunky) Kasner of south Minneapolis have been diagnosed with Duchenne Muscular Dystrophy. Duchenne is …
Rare Duchenne Muscular Dystrophy Mutation Has New Tx ...
https://www.medpagetoday.com/neurology/generalneurology/88038
Aug 12, 2020 · "The FDA is committed to fostering drug development for serious neurological disorders like Duchenne muscular dystrophy," Billy Dunn, MD, director of …
FDA Approves NS Pharma’s Viltepso for Duchenne Muscular ...
https://www.biospace.com/article/fda-approves-ns-pharma-s-viltepso-for-duchenne-muscular-dystrophy/
Aug 13, 2020 · The U.S. Food and Drug Administration (FDA) approved another therapy for Duchenne muscular dystrophy (DMD), this time NS Pharma’s Viltepso (viltolarsen). NS Pharma is a wholly owned subsidiary of Nippon Shinyaku Co. DMD is a muscle-wasting disease caused by mutations in the dystrophin gene.
Sarepta Therapeutics Announces FDA Acceptance of ...
https://www.globenewswire.com/news-release/2020/08/25/2083264/0/en/Sarepta-Therapeutics-Announces-FDA-Acceptance-of-Casimersen-SRP-4045-New-Drug-Application-for-Patients-with-Duchenne-Muscular-Dystrophy-Amenable-to-Skipping-Exon-45.html
Aug 25, 2020 · Duchenne muscular dystrophy is a rare, fatal neuromuscular genetic disease that occurs in approximately one in every 3,500-5,000 males worldwide. Duchenne is caused by a change or mutation in the ...
The History — Fight Duchenne Foundation
http://www.fightduchenne.org.au/the-history
The Tour Duchenne has a simple mission: To assist Duchenne Muscular Dystrophy boys and girls and their families with services, facilities and respite care through raising maximum funds and awareness nationally. Tour Duchenne is the way in which we achieve this vision!
DuchenneXchange join our Duchenne Muscular Dystrophy ...
https://www.duchennexchange.org/
The mission: Cure Duchenne muscular dystrophy Making our voices heard DuchenneXchange is your source for up-to-date information on Duchenne muscular dystrophy, connecting with new and ongoing clinical trials, and meeting others in the community
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