Search results for #Duchenne
$SRPT 8. #Elevidys (delandistrogene moxeparvovec-rokl), that is with a severely restricted label and first commercial dose administered last August. 💪#Duchenne #GeneTherapy
$SRPT 8. #Elevidys (delandistrogene moxeparvovec-rokl), that is with a severely restricted label and first commercial dose administered last August. 💪#Duchenne #GeneTherapy
PPMD Together meetings are about coming together and shaping a future where every individual affected by #Duchenne and #Becker can thrive. Thank you to all who joined us for these important, heartfelt discussions in Cincinnati. Learn more: parentprojectmd.org/catch-up-on-pp…
📆 2024 Annual General Meeting: Join us online on Monday, June 3, as we reflect on our collective efforts in advancing our mission to defeat #Duchenne #musculardystrophy. Let's come together to build momentum for the work ahead: bit.ly/3xeeaXy.
Read more about our plan to optimize care and improve outcomes for Muscular Dystrophy patients here: bit.ly/3wh5rDV! #PedsHF #ACTIONMuscularDystrophy #Duchenne #MuscularDystrophy #EndDuchenne
PPMD is excited to announce a $250,000 award to Bo Hoon Lee, MD, from the @UR_Med to support the development of a clinical research network for #Duchenne babies identified through #newbornscreening efforts in New York State. parentprojectmd.org/ppmd-awards-25…
This is the reality of a Duchenne diagnosis: Eventually, it takes all. At Defeat Duchenne Canada, we have hope for a brighter future for everyone with a #Duchenne #musculardystrophy diagnosis. Invest in a world without Duchenne: bit.ly/3IVF5dd.
His words, his bravery, his "ask", are etched in my mind forever ❤️ #Eteplirsen #pioneer #trailblazer #Duchenne #exondys51 #raredisease
Résultats positifs pour la phase I/II de l'essai de thérapie génique mené par @GenethonFr dans la myopathie de #Duchenne @Myology2024 afm-telethon.fr/fr/actualites/…]
Thank you to all who have submitted applications for our 2024 Research Grant Program! Our team is hard at work reviewing each submission focused on improving the lives of those with #Duchenne #musculardystrophy. Research funded by Defeat Duchenne Canada: bit.ly/3UbRRbF
$SRPT maybe a good time to repost this for the newbies or #ICYMI #GeneTherapy #Duchenne #ThrowbackThursday x.com/jonu235/status…
$SRPT maybe a good time to repost this for the newbies or #ICYMI #GeneTherapy #Duchenne #ThrowbackThursday x.com/jonu235/status…
Register by midnight TOMORROW to receive your FREE t-shirt delivered to your door for Walk day – Sunday, May 26. Support the fight to save the lives of all the boys we know and love living with #Duchenne #musculardystrophy. Register now: bit.ly/4bFYnR2.
$SRPT Professor Dr. Jerry Roy Mendell - Medicine Winner King Faisal Prize @nationwidekids @KingFaisalPrize💪💪💪#Elevidys #GeneTherapy #Duchenne #RareDisease youtube.com/watch?v=hn5RWP…
$SRPT "As Luis and Manuela sighed in relief, they saw a new Lucas emerge." 💪💪💪#Elevidys #GeneTherapy #Duchenne #RareDisease @BostonChildrens Lucas receives gene therapy for DMD and finds his super muscles answers.childrenshospital.org/dmd-gene-thera…
Over the course of the next two days, we'll be at the 17th Annual Pediatric Neurology Symposium with @LeBonheurChild. We look forward to engaging in meaningful discussions on how to improve diagnoses and enhance treatment plans in #Duchenne and other nervous system disorders.