Similar organisations to Ohio Sickle Cell Health Association Inc
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Single Organization Support
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766.
University of Iowa Research Foundation
THE UNIVERSITY OF IOWA RESEARCH FOUNDATION'S (UIRF) MISSION IS TO: ADVANCE, DEVELOP, INCREASE AND EXTEND THE PROGRESS OF SCIENCE AND USEFUL ARTS THROUGH ENCOURAGING AND ASSISTING INVESTIGATION, RESEARCH AND EDUCATION AT THE STATE UNIVERSITY OF IOWA BY FURNISHING THE MEANS, METHODS AND AGENCIES BY WHICH IDEAS, CREATIONS, DISCOVERIES, INVENTIONS AND PROCESSES MAY BE PROTECTED AND THE USES THEREOF DETERMINED AND SAFEGUARDED FOR THE PUBLIC, AND TO MANAGE, LICENSE AND DISPOSE OF PROPRIETARY RIGHTS IN IDEAS, CREATIONS, DISCOVERIES, INVENTIONS AND PROCESSES OF ANY NATURE; TO RECEIVE BY GIFT, GRANT, DEVISE OR BEQUEST, AND TO ACQUIRE BY PURCHASE, LEASE, EXCHANGE OR OTHERWISE, PROPERTY, BOTH REAL AND PERSONAL, EITHER AS ABSOLUTE OWNER OR AS TRUSTEE THEREOF, AND TO MANAGE AND ADMINISTER THE SAME; TO MAKE CONTRIBUTIONS, GRANTS, GIFTS AND TRANSFERS OF PROPERTY, BOTH REAL AND PERSONAL, EITHER OUTRIGHT OR IN TRUST, TO OR FOR THE BENEFIT OF THE STATE UNIVERSITY OF IOWA.
Iowa City
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Diseases, Disorders, Medical Disciplines N.E.C.
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767.
Cascade Foundation of Southern Arizona Inc
Non profit focused on providing a local support system for the bleeding disorder community in southern Arizona.
404
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Cancer Research
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768.
The Leukemia & Lymphoma Society
United in progress toward a world without blood cancer.
554862
Rye Brook
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Birth Defects, Genetic Diseases
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769.
Kentucky Hemophilia Foundation Inc
The Kentucky Hemophilia Foundation assists individuals with hemophilia and similar bleeding disorders through education, advocacy, and support services and by promoting research for a cure.
Louisville
Prader-Willi Syndrome Association | USA
What’s YOUR story. Tweet us and tell us what it’s like #GrowingUpRare We hope you will suggest the PWSA | USA facebook page to your friends.
16178
Legal name of organization: Prader-Willi Syndrome Association | USA
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Alliance/Advocacy Organizations
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771.
ALVEOLAR CAPILLARY DYSPLASIA ASSOCIATION
This ACDA site is the social media outreach for parents of ACD patients during any treatment phase and support system for those experiencing child loss.
1600
Huntersville
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Birth Defects, Genetic Diseases Research
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772.
International Association for Chronic Fatigue Syndrome-Me
THE MISSION OF IACFS/ME IS TO PROMOTE, STIMULATE AND COORDINATE THE EXCHANGE OF IDEAS RELATED TO CHRONIC FATIGUE SYNDRONE(CFS) AND FIBROMYALGIA(FM) RESEARCH, PATIENT CARE AND TREATMENT IN ADDITION, THE IACFS/ME PERIODICALLY REVIEWS THE CURRENT RESEARCH AND TREATMENT LITERATURE AND MEDIA REPORTS FOR THE BENEFIT OF SCIENTISTS, CLINICIANS AND PATIENTS.
Stony Brook
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Fund Raising and/or Fund Distribution
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773.
Childrens Rare Disease Organization Inc
Many children are living with a rare disease.
Potomac
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Nerve, Muscle, and Bone Research
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774.
GIVING STRENGTH INC
Every dollar raised and donation made will make a major impact on future research for congenital muscular dystrophy subtype, SELENON.
487
FULTON




