Similar organisations to 24 Hours for Hank Inc
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Public Foundations
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388.
Sunbeam Foundation
Fighting Rare and Underfunded Pediatric Cancer Our purpose is to identify and support cuttingedge research aimed at finding a cure for Ewings Sarcoma and other forms of pediatric bone cancer.
98
Mountain View
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Museums & Museum Activities
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389.
Histiocyte Society
The Histiocyte Society is a group of physicians and scientists committed to clinical and laboratory research into causes and treatment of histiocytic disorders.
556
Pitman
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Alliance/Advocacy Organizations
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390.
The Foundation for Orthopaedics and Regenerative Medicine
To conceive and carry out cutting edge clinical research to advance the fields of Orthopaedics and Regenerative Medicine, and provide education to medical professionals and the public.
GLENVIEW
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Birth Defects, Genetic Diseases
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391.
Project Dna A Nonprofit Corporation
Project DNA is dedicated to creating programs to screen, identify and enable physicians to take care of their patients with hereditary cancer syndromes Home Genes TyrerCuzick Model Patients Physicians Diagnostic Criteria More Project DNA We cant change your family history but we can change your familys future.
323
Monterey
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Specifically Named Diseases
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392.
USHER 2020 FOUNDATION INC
Bringing therapies into clinical trials for those losing vision due to Usher Syndrome and retinitis pigmentosa.
764
Atlanta
BARROW NEUROLOGICAL FOUNDATION
Our mission is to be the catalyst of our donors’ passion for transformation by providing the resources for Barrow Neurological Institute to achieve its mission.
49962
Phoenix
Foxg1 Research Foundation
FOXG1 syndrome is a childhood neurological genetic disorder and is a key to understanding many brain disorders.
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Sands Point
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Human Services - Multipurpose & Other N.E.C.
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395.
Movement Disorders Foundation of Arizona
MDFA aims to enrich the lives of those with movement disorders.
2713
Scottsdale
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Public Foundations
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396.
CURING RETINAL BLINDNESS
Welcome to our mission of bringing sight to children who are blind or visually impaired due to CRB1 retinal disease.
1379
SALEM






