John Walton Muscular Dystrophy Research Centre John Walton Muscular Dystrophy Research Centre
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Neuromuscular disease is rare compared with other disease s. Three or four persons in 100.000 inhabitants live for example with the muscle dystrophy
Duchenne Muscular Dystrophy - Jesse's Journey - The Foundation for Gene and Cell Therapy provides funding for research into Duchenne Muscular Dystrophy. This charitable organization targets neuromuscular diseases like Duchenne MD through research in gene therapy, cell therapy and genetics.
Duchenne Muscular Dystrophy (DMD) is a progressive genetic muscular system disease that affects 1 in every 5, 000 boys.
Children's Dentist Sacramento Carmichael Citrus Heights Fair Oaks is a pediatric dentist in Sacramento, California, dedicated to serving the special needs
Pharmaceutical company in Switzerland committed to research & development of medicines for patients living with mitochondrial disorders & rare diseases.
Our kids our nation is an exquisite coffee table book that features our Australian children. It is a unique fundraising project for Muscular Dystrophy Australia. Children from newborn to 15 years old will be professionally photographed by an accredited photographer. One of the images taken of your child will be guaranteed to appear in this book.
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AFM-Téléthon is an association composed of patients and their families who are affected by a genetic, rare, progressive and severely disabling disease
WiViK on-screen keyboard (virtual keyboard) software is an assistive technology that can help persons such as those with spinal cord injuries, ALS, muscular dystrophy, and cerebral palsy who cannot use a standard computer keyboard.
Charley's Fund accelerates the development of life-saving treatments for Duchenne muscular dystrophy and supports solutions to translate promise into results.
Misty Vanderweele grows premium Dahlias, Sweetpeas, Sunflowers/ other cut flower varieties. Dedicated to providing long-lasting vibrant arrangements & bouquets.
Angels for Isaac works to educate the public about Duchenne Muscular Dystrophy and how they can help in our fight to find a cure. We have kicked off our 2014 RZR Raffle. Purchase your ticket to help us put an END to Duchenne Muscular Dystrophy, a terminal muscle wasting disease with no treatment and no cure!
The Neurology Muscular Dystrophy and Neuropathy Institute, headed by Doctor Natan Shaoulian, The Nerve MD. USC trained, Dr. Shaoulian is a board certified Neurologist subspecializing in neuromuscular disorders. Located in Beverly Hills California