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Information about a foundation dedicated to increasing awareness of Sanfilippo Syndrome and raising funds to support research aimed at finding a cure. Includes a ...

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 Cystinosis Foundation UK is a charity concerned with promoting awareness of Cystinosis and supporting both families and medical research within the United ...

Personal site about a child with this disorder. Provides details about the condition.

Jonah's Just Begun supports research for Sanfilippo Syndrome (MPS III), a rare genetic disease.Jonah Weishaar

The PAF is an organization that funds academic and medical research leading to better treatments and a cure of propionic acidemia, an inborn error of metabolism.

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Clinical experts provide current medical information and news on health topics.