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Sanfilippo Syndrome (7) See Also:
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Sites:
» Ben's Dream
Information about a foundation dedicated to increasing awareness of Sanfilippo Syndrome and raising funds to support research aimed at finding a cure. Includes a newsletter. http://www.bensdream.org » Bennett Children's Foundation
Founded by parents of three young children who suffer from Sanfilippo Syndrome, a degenerative genetic disorder that is usually fatal before the teens. Raising awareness of the condition and enlisting financial support. http://www.claritystudio.com/helpachild/ » Children's Medical Research Foundation
Funds medical research to find a cure for Sanfilippo Syndrome and other neuro-genetic disorders. News and links to summaries of research that has been supported by the foundation. http://www.curekirby.org/ » Frankiepants
Personal site about a child with this disorder. Provides details about the condition. http://www.frankiepants.com » Jonah's Just Begun
The parents of Jonah Weishaar, who has the rare genetic disease Sanfilippo Syndrome, are setting up the Foundation to Cure Sanfilippo to undertake research into the condition. http://www.jonahsjustbegun.org » MPS III
Information, including the causes, different forms, the inheritance and how the disorder progresses. http://www.mpssociety.org/content/4039/MPS_III/ » The Sanfilippo Children's Research Foundation
Canadian based charitable group founded by the parents of Elisa Linton. http://www.alifeforelisa.org/ This category needs an editor
Last Updated: 2010-07-15 20:59:41
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