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November 19, 2024
Regenxbio Gears Up to Challenge Sarepta in DMD as Gene Therapy Advances to Pivotal Studies (BioSpace)November 18, 2024
FDA endorses speedy approval path for Regenxbio Duchenne gene therapy (BioPharma Dive)November 17, 2024
OC500 2024: PAUL AND DEBRA MILLER (Orange County Business Journal)November 15, 2024
I Just Watched The Remarkable Life of Ibelin, And I Was So Moved By How Role-Playing Games Can Empower People with Disabilities (CinemaBlend)November 14, 2024
They thought their son lived an isolated life. But when he died, friends showed up in droves. (Upworthy)November 5, 2024
FDA Accepts Resubmitted NDA for Ataluren in Nonsense Duchenne Muscular Dystrophy (NeurologyLive)November 1, 2024
New Partnership Brings Hope for Duchenne Muscular Dystrophy (Treat-NMD)October 30, 2024
Grandmother Helps Raise $100,000 for Duchenne Muscular Dystrophy Research (Inspire More)October 29, 2024
CureDuchenne partners with Blizzard Entertainment and World of Warcraft for limited-time charity pet program (Rare Revolution Magazine)October 29, 2024
CureDuchenne Partners with World of Warcraft to Showcase the Power of Online Friendships (DESIGNRUSH)October 28, 2024
WOW: SUPPORT CUREDUCHENNE WITH THE REVEN PACK (GameSpace)October 26, 2024
World of Warcraft Reveals Adorable New Charity Bundle (Game Rant)October 24, 2024
Debra Miller: OC Visionary (Los Angeles Times)October 21, 2024
Austin’s “Afternoon in NYC” Luncheon Raises $90K for Duchenne Research (Tribeza)October 16, 2024
13th Annual Getzlaf Golf Shootout Raises Nearly $500K for CureDuchenne (Newport Beach Independent)October 9, 2024
As U.S. efforts stall, China pushes ahead with CRISPR treatments for muscular dystrophy (STAT)October 3, 2024
Study Suggests More DMD Trials Should Include Patients Who Can’t Walk (Rare Disease Advisor)September 23, 2024
Defying Duchenne (Raising Arizona Kids)September 19, 2024
Calves to Cure helps fund research for Worden boy’s rare disease (KTVQ Billings)September 7, 2024
Helping to Expand Global Care for the Duchenne Muscular Dystrophy Patient Community: Debra Miller (NeurologyLive)September 7, 2024
One Step at a Time: Tucson child receives gene therapy for Duchenne (ABC 9 Tucson)September 7, 2024
Real-World Experience With Duchenne Muscular Dystrophy Gene Therapy (CGTlive)