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A life For Elisa
描述: Canadian based charitable group founded by the parents of Elisa Linton.
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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 ...
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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 ...
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The Cystinosis Foundation UK is a charity concerned with promoting awareness of Cystinosis and supporting both families and medical research within the United ...
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Personal site about a child with this disorder. Provides details about the condition.
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Jonah's Just Begun supports research for Sanfilippo Syndrome (MPS III), a rare genetic disease.Jonah Weishaar
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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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Get breaking national and world news, broadcast video coverage, and exclusive interviews. Find the top news online at ABC news.
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Clinical experts provide current medical information and news on health topics.
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