Duchenne Muscular Dystrophy Websites
The Leader in RNA-based Medicine | Sarepta Therapeutics
We develop RNA-based therapeutics to improve the lives of people affected by serious diseases; this includes eteplirsen for the treatment of DMD.
Not Applicable
$
8.95
The Leader in RNA-based Medicine | Sarepta Therapeutics
We develop RNA-based therapeutics to improve the lives of people affected by serious diseases; this includes eteplirsen for the treatment of DMD.
Not Applicable
$
8.95
Sarepta Therapeutics | Focused on precision genetic medicines to treat
Sarepta is at the forefront of precision genetic medicine, having built an impressive and competitive position in Duchenne muscular dystrophy (DMD) and more recently in gene therapies for 5 Limb-girdle muscular dystrophy diseases (LGMD), Charcot-Marie-Tooth (CMT), MPS IIIA, Pompe and other CNS-related disorders, totali
341,531
$
25,920.00
Home Page
Duchenne San Diego :. Non-Profit Charity for the Benefit of Duchenne Muscular Dystrophy
Not Applicable
$
8.95
DMD Fund - Duchenne Muscular Dystrophy Fund
DMD Fund - Duchenne Muscular Dystrophy Research Fund - Helping Research to fight the most common fatal genetic disease of children
17,023,671
$
8.95
The Eileen McCallum Trust
The Eileen McCallum Trust is a Scottish charity devoted to providing support for boys and young men living with the condition Duchenne muscular dystrophy (DMD).
Not Applicable
$
8.95
Mary-Lou Weisman - Prize Winning Journalist, Best-Selling Author and D
Mary-Lou Weisman is a prize-winning journalist and best-selling author of Intensive Care, Traveling While Married, My Baby Boomer Baby Book, and Al Jaffee's Mad Life.
Not Applicable
$
8.94
RARE-e-CONNECT - RARE-e-CONNECT
Secure multidisciplinary collaboration and knowledge sharing on rare diseases. For Healthcare Professionals and patients within Cyprus and abroad, large repository of medical centres in Europe and other countries with verified expertise in rare disease groups and rare diseases, Patient life stories, Continuous Medical
Not Applicable
$
8.95
MDCRC - Molecular Diagnostics Counseling Care and Research Center
Molecular Diagnostics, Counseling, Care and Research Center- MDCRC
Not Applicable
$
8.95
The Andrew's Hope Fund, Harvesting Hope for Andrew
a site to raise funds for our son, Andrew who is diagnosed with Duchenne Muscular Dystrophy, you can make a donation or register for our 5k race
Not Applicable
$
8.95
Greg Marzolf Jr. Foundation
Helping people with Muscular Dystrophy
Not Applicable
$
8.95
Kids Neuro Care Clinic in Ludhiana,
Kids Neuro Care Clinic in Ludhiana, India - ; Get Latest Updates and offers, Contact, Address, Ratings, Location, Maps for Kids Neuro Care Clinic;
Not Applicable
$
8.95
Adult Stem Cell Research
Featuring the latest stem cell research success stories. Also provides stem cell therapy and treatment information!
Not Applicable
$
8.95
Nash Avery Foundation - Committed to the destruction of Duchenne Muscu
Enter the website of the Nash Avery Foundation. Committed to the destruction of Duchenne Muscular Dystrophy.
Not Applicable
$
8.95
EndDuchenne.org - Leading the fight to end Duchenne muscular dystrophy
Parent Project Muscular Dystrophy's mission is to end Duchenne muscular dystrophy. We accelerate research, raise our voices in Washington, demand optimal care for all young men, and educate the global community.
Not Applicable
$
8.95
Adult Stem Cell Research
Featuring the latest stem cell research success stories. Also provides stem cell therapy and treatment information!
Not Applicable
$
8.95
Nash Avery Foundation - Committed to the destruction of Duchenne Muscu
Enter the website of the Nash Avery Foundation. Committed to the destruction of Duchenne Muscular Dystrophy.
Not Applicable
$
8.95
