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EBMRF - Epidermolysis Bullosa Medical Research Foundation
opis: The EBMRF is a volunteer, non-profit Foundation dedicated to helping medical scientists learn more about EB, its causes, the development of successful treatments, and ultimately, its cure.
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język: English
tematy stron: conditions
The Dystrophic Epidermolysis Bullosa Research Association of America (debra), the only national non-profit dedicated to funding research and providing services and ...
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Information, mailing list, pictures, and help for new parents.
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An organization where people with albinism, their families and those that work with them can get information, ask questions and share their experiences.
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Features organization background, information about the disorder, fundraising and research details, and news.
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A small group of relatives and friends of EB patients founded DEBRA Canada in 1998. That informal group has evolved into a Board of 10 people who meet monthly to ...
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Progeria: A very rare terminal condition. From the Greek meaning "prematurely old". Characterized by an appearance of accelerated aging. This Web Site is ...
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Dystrophic Epidermolysis Bullosa Research Association. A voluntary, non-profit organization dedicated to creating awareness and providing support for families ...
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The leading source for trustworthy and timely health and medical news and information. Providing credible health information, supportive community, and educational ...
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4.5 / 5.0, język: English
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