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Research and Markets: Fragile X Syndrome Global Clinical Trials Review, H2, 2011
Research and Markets has announced the addition of GlobalData's new report "Fragile X Syndrome Global Clinica -
Earlier detection of Fragile X syndrome made possible
Now families children with fragile X syndrome may have a chance of earlier detection and intervention. The Murdoch Children's Research Institute breakthrough could allow newborn screening of the world's most common cause of inherited developmental disability. The research findings were published in the journal Clinical Chemistry. -
New hope in diagnosis of rare disorder
A genetic test developed by Aust researchers could diagnose the disorder Fragile X Syndrome, at birth. -
Your Health: Fragile X marks the spot
Its called Fragile X Syndrome and its associated with autism. Now a new treatment is offering kids a new lease on life. -
Oh No They Didn't! NFXF Launches New Web Site, Logo and First Brand Tagline
WALNUT CREEK, Calif. , Jan. 17, 2012 /PRNewswire/ -- The National Fragile X Foundation, the world's leading authority on fragile X syndrome, launched its new website today. The site, FragileX.org, has ... -
Help for fragile X victims
A WORLD first test will give thousands of families affected by fragile X syndrome the chance of earlier detection and intervention. -
Breakthrough in diagnosis of autism
MELBOURNE researchers have developed a new test to diagnose the genetic disorder Fragile X syndrome, the most common inherited cause of autism. The syndrome, which affects about 70,000 Australians, is currently difficult to diagnose in girls, who may carry the gene but are largely free of symptoms. -
The RARE List(TM) - You Must See it to Believe it!
7,000 Different Rare Diseases and Disorders Comprise 65 Page RARE List(TM), 95% of the Medical Conditions Included on RARE List(TM) Have No FDA Approved Treatments -
Making New Friends
CLEVELAND Jackie Mayer of Cleveland knows how difficult it is for families to attend social events when they have a child with developmental disabilities. Her 10-year-old son, Dillon, has a genetic disorder called Fragile X Syndrome, and his behavior makes it hard to go places as a family. -
RNAi - Technologies, Markets and Companies
NEW YORK, Feb. 1, 2012 /PRNewswire/ -- Reportlinker.com announces that a new market research report is available in its catalogue: RNAi - technologies, markets and companies http://www.reportlinker.com/p0203551/RNAi---technologies-markets-and-companies.html#utm_source=prnewswire&utm_medium=pr&utm_campaign=Biological_TherapyRNA ...
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Important Information
Contained within this section of our Web site is a collection of disability-specific resources, headlines, news summaries and news sources. A click to a related link queries Web sites around the world. These sites often have a lot of activity, so the query may take a short while to produce results. Patience will be rewarded!
Some articles are unrelated to disabilities even though search terms such as "disabilities" and "Massachusetts" appear within them. Currently, there is no way to exclude them.
