Similar organisations to The Shank2 Foundation
THE NEUROMUSCULAR DISEASE FOUNDATION
NDF is a nonprofit whose mission is to raise awareness and encourage testing for HIBM and to find a cure for neuromuscular diseases, including HIBM.
6814
Beverly Hills
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Alliance/Advocacy Organizations
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236.
The Cute Syndrome Foundation, Inc.
The Cute Syndrome Foundation raises awareness of SCN8A mutations, funds the dedicated and talented scientists researching SCN8A, and supports the families around the world who are affected by SCN8A-related disorders.
9100
Ozark
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Autism
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237.
N of One
N of One: Autism Research Foundation is a leading research non-profit that sponsors breakthrough autism research https://t.
5746
Dallas
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Alliance/Advocacy Organizations
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238.
Coffin-Siris Syndrome Foundation
Coffin-Siris Syndrome Foundation is a 501c3 that exists to connect, support, and inform those affected by Coffin-Siris Syndrome and related disorders and promote related research.
3400
KIRKLAND
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Nerve, Muscle, and Bone Diseases
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239.
Bodor Research Foundation
THE PRIMARY ACTIVITY OF BODOR RESEARCH FOUNDATION IS THE FURTHERANCE OF CHARITABLE, SCIENTIFIC, AND ADVANCEMENT OF EDUCATION AND SCIENTIFIC PURPOSES, THROUGH RESEARCH PROJECTS TO DEVELOP AND TEST ALTERNATE TECHNIQUES FOR TREATMENT OF NEUROMUSCULAR AND MUSCULOSKELETAL DISORDERS, AND BY PUBLISHING PAPERS ON THE FINDINGS.
Napa
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Specifically Named Diseases Research
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240.
Sleep Consortium
Sleep Consortium accelerates next-generation research and therapy development for Central Disorders of Hypersomnolence through a data collection ecosystem.
45
West Palm Beach
Friends of FSH Research
Volunteer Run non-profit funding FSH Muscular Dystrophy research.
620
Kirkland
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Neurology, Neuroscience
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242.
SALK INSTITUTE FOR BIOLOGICAL STUDIES
The Salk Institute for Biological Studies is one of the world's preeminent basic research institutions.
56670
La Jolla
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Birth Defects, Genetic Diseases
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243.
Skraban-Deardorff Syndrome Foundation
The Skraban-Deardorff Syndrome Foundation has been formed by parents and medical professionals worldwide to foster relationships and organize resources to benefit individuals with Skraban-Deardorff Syndrome.
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