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Welkom bij dystrophie-de-fuchs.be
Muscular Dystrophy Tasmania | Muscular Dystrophy Tasmania
Muscular Dystrophy Australia Muscular Dystrophy Assoc
Muscular Dystrophy Australia (MDA) the one stop shop for information and support for people living with neuromuscular diseases.
Author: Boris M Struk
Muscular Dystrophy News Home - Muscular Dystrophy News
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Author: Theme Templates
Muscular Dystrophy Association
MDA is the nonprofit health agency dedicated to curing muscular dystrophy, ALS and related diseases by funding worldwide research.
Myotonic Dystrophy Foundation
Helping families living with myotonic dystrophy by delivering comprehensive support resources, and driving research to accelerate the discovery of DM therapies.
Muscular Dystrophy UK
Spinraza Muscular Dystrophy
Spinraza Muscular Dystrophy,SMA Clinical Trials,Spinal Muscular Atrophy Therapy,Spinal Muscular Atrophy Treatment
Dystrophy Annihilation Research Trust – Aspiring to achieve Total Annihilation of Muscular Dystrophy
Aspiring to achieve Total Annihilation of Muscular Dystrophy
QU’EST-CE QUE LA DYSTROPHIE MUSCULAIRE DE DUCHENNE?
MDSA - The Muscular Dystrophy Foundation of SA
Leiden Muscular Dystrophy Pages
Myotone Dystrophie – Selbsthilfegruppe Nordwestschweiz
MIND Trust - Mobility in Dystrophy
Home - Muscular Dystrophy Foundation Australia
Author: Admin
The Diagnosis and Management of Duchenne Muscular Dystrophy
CARE-NMD: Improving care for Duchenne muscular dystrophy
Improving care for Duchenne muscular dystrophy
Home - Muscular Dystrophy Association (Singapore)
Reflex Sympathetic Dystrophy - RSD Foundation
The International Research Foundation for RSD / CRPS is a not-for-profit organization (501c3) dedicated to education and research on Reflex Sympathetic Dystrophy and Complex Regional Pain Syndrome.
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Bietti's Crystalline Dystrophy - Resources and Community
A Call to Action to find the fix to BCD
Home - Myotonic Dystrophy Support Group
Muscular Dystrophy Foundation of South Africa
Official Website of MDC | Muscular Dystrophy Canada
Duchenne UK - Bringing an end to Duchenne muscular dystrophy
Duchenne UK is the leading UK charity for Duchenne muscular dystrophy. We're going further and faster than ever before to find effective treatments for DMD.
Cure CMD | Congenital Muscular Dystrophy Research
CMD, col6, col12,lama2,selenon,sepn1,alpha-dystroglycanopathy,lmna
Michael's Cause – Fighting Duchenne Muscular Dystrophy
Fighting Duchenne Muscular Dystrophy
The Speak Foundation - Limb Girdle Muscular Dystrophy
Established in 2008, The Speak Foundation is the first patient led organization to help those living with Limb Girdle Muscular Dystrophy and other forms of NMD.
Author: The Speak Foundation
Muscular Dystrophy Queensland | We're stronger together.
Buyyour MDQ products online today Thanks for your interest in helpingpeople living withneuromuscular conditions. With your help, we're able to provide a
The French Muscular Dystrophy Association (AFM-Téléthon)
AFM-Téléthon is an association composed of patients and their families who are affected by a genetic, rare, progressive and severely disabling disease
Home | Muscular Dystrophy Association of New Zealand
MDANZ is a member led, not for profit organisation, that provides resources, information and support to individuals and whanau with lived experience of neuromuscular conditions. We have four regional branches throughout the country which are supported by the National Office based in Auckland.
Kurt+Peter Foundation | Muscular Dystrophy | LGMD2C
The Kurt+Peter Foundation funds research to treat or cure LGMD2C. The foundation works with top tier research institutions and biotechnology companies.
Jesse's Journey | Duchenne Muscular Dystrophy | Canada
Duchenne Muscular Dystrophy (DMD) is a progressive genetic muscular system disease that affects 1 in every 5,000 boys.
Rock for Hope - Muscular Dystrophy Benefit Concert
Euro-DyMA – Federation of European Myotonic Dystrophy Associations
Muscular Dystrophy | Laughing At My Nightmare, Inc. | United States
Laughing At My Nightmare is a 501(c)3 nonprofit dedicated to providing equipment to those living with muscular dystrophy and teaching students that all people deserve kindess and respect, regardless of their differences.
Muscular Dystrophy | Neuromuscular Condition | Spinal Muscular Atrophy
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Facioscapulohumeral Muscular Dystrophy Info - Treatment - FSHD Society
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Facioscapulohumeral Muscular Dystrophy
- UK Patient Registry for FSHD
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Nail dystrophy affects millions. Take control of your nail problems with our resources on brittle, split, peeling & fragile fingernails.
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Parent Project Muscular Dystrophy (PPMD) | Fighting to End Duchenne
Parent Project Muscular Dystrophy fights to end Duchenne. We accelerate research, raise our voices to impact policy, demand optimal care for every single family, and strive to ensure access to approved therapies.
Indian Association of Muscular Dystrophy Solan | Symptoms | IAMD
Muscular dystrophy is a progressive neuromuscular genetic disorder. Know more about its initial symptoms & what indian association of muscular dystrophy does to provide relief.
Alex's Wish | fundraising charity for Duchenne Muscular Dystrophy
Alex’s Wish is a charity set up to eradicate Duchenne Muscular Dystrophy, an aggressive form of Muscular Dystrophy that affects 1 in every 3,500 boys born and results in total paralysis. Established by Emma and Andy Hallam (parents to Alex) in late 2012, Alex's Wish helps raise vital funds to help bring about new treatments and ultimately a cure for this devastating condition.
Aged Care Service, Massage Therapy, Muscular Dystrophies Therapy Sydney
Mega Therapy providing aged care service, massage therapy, relaxation massage, and Muscular Dystrophies Therapy Sydney. Contact us today to avoid problems with your health tomorrow.
Duchenne Muscular Dystrophy Foundation (Duchenne SpierDystrofie Stichting) - Home
WE are so glad that you visit this site of DUCHENNE MUSCULAR DYSTROPHY. This is a registered Humanitarian FOUNDATION located in the country of SURINAME SOUTH AMERICA. WE are here to help you and your loved ones to have HOPE as you face the challenges in
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Manipulating Cell Signaling For Better Muscle Function In Muscular Dystrophy From
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Joining Jack - Join Jacks' fight against Duchenne Muscular Dystrophy
Jack has Duchenne Muscular Dystrophy, DMD. There is no cure at the moment. We're raising money to fund research to find effective treatments
Muscular Diseases Awareness – Information about muscular dystrophies and other diseases research
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Wij zijn Het Streek, dé christelijke scholengemeenschap in Ede en omgeving met hart voor onderwijs en mensen. Dat zie je en voel je wanneer je bij ons komt.
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