
Sarepta Therapeutics
@sarepta
Commercial-stage biopharma company focused on the discovery & development of precision genetic medicine to treat rare neuromuscular diseases. bit.ly/3XgXshH
ID: 2216555822
http://sarepta.com 26-11-2013 21:45:22
1,1K Tweet
5,5K Followers
62 Following

Muscular Dystrophy UK
@mduk_news
We connect a community of over 110,000 people living with muscle wasting and weakening conditions. Together we are stronger. Join us. Our #MusclesMatter.
paolo cecchelin
@piccolone

CureDuchenne
@cureduchenne
We are committed to improving the lives of those affected by Duchenne through accelerating research, improving care and empowering the community.
Parent Project Muscular Dystrophy (PPMD)
@parentprojectmd
Let's advance the research evolution. #EndDuchenne
Muscular Dystrophy Association
@mdaorg
MDA is the #1 voluntary health organization in the United States for people living with #MuscularDystrophy, #ALS, and related #neuromuscular diseases.
Virginia Arechavala
@varechavala
Scientist and mum. @ikerbasque Professor @biocrucesHR Interested in #RNAtherapy for #neuromuscular disorders. De Bilbao de toda la vida and adopted Londoner.
Alexander Yang
@alexyang19

Adam K
@bikepeddle
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@gantosj
Equity market consultant. Technical Analysis Trader with over 25 years of experience. #Biotech Deep dive research. Biotech Trading Analyst @ChimeraResearch
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Retired, Bio/Chemistry guy.
Relay 70F
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Duchenne UK
@duchenneuk
Duchenne UK has one clear aim – to end Duchenne, a devastating muscle-wasting disease. We are the leading Duchenne muscular dystrophy charity in the UK.
Terri Ellsworth
@terriellsworth
Duchenne Advocate/Rare Disease Activist Mom, Designing Mom-Creating awareness & advocating for approval of safe & effective drugs. Words are always my own.
ASGCT
@asgctherapy
Advancing knowledge, awareness, and education leading to the discovery and clinical application of genetic and cellular therapies to alleviate human disease.
Pedro
@psaenzm

Oligonucleotide Therapeutics Society
@otsociety
A nonprofit forum to foster academia and industry based research and development of oligonucleotide therapeutics.
Daren
@ragdaren71

Matthew S. Alexander
@matt_muscle_guy
Geneticist, Skeletal Muscle, Drug development, Gene therapies. Non-coding RNA, and Zebrafish Aficionado. All tweets are my own. Instagram @thealexanderlab
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LGMD Awareness Foundation, Inc
@lgmdawareness
A 501(c)(3) advocacy organization dedicated to globally raising awareness of the rare neuromuscular diseases known as Limb-girdle muscular dystrophy (LGMD).
World Muscle Society
@worldmusclesoc
The WMS is a global, multidisciplinary community committed to advancing the science of neuromuscular disorders. Join us in Vienna for #WMS2025.
AnnemiekeAartsma-Rus
@oligogirl
Translating science from bench to bedside and from jargon to lay language
World Duchenne Organization
@worldduchenne
Global organization to find a cure and viable treatment for those lives affected by dystrophinopathies: Duchenne and Becker Muscular Dystrophy. RT ≠ endorsement
Lgmd'li birey 💚💚💚
@lgmdder
LGMD ilerleyen bir kas hastalığıdır.
Patient_Investor
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Phd student at @IVS_ffm
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Byron On X
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Private Investor
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أقاتل ضمور العضلات الحزامي (LGMD2D) بكل أمل وإصرار 💪 | رحلة علاج جيني في أمريكا 🇺🇸 | شاركوني الدعاء والدعم gofundme.com/f/support-anwa…
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aditi siddha
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Ömer ASAF ULUDAĞ
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Aliziiiimos
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When it comes to the end, you’re just same as them
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it could be
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HL
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Drewbie.sui
@metadrewbie
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tomtomtomtom123
@tomtomtomtom123

Roni
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Ronj
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@piero_le_chat
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