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Research into Fragile X Syndrome - discoveries, clinical trials
Updated on 2009-09-21
Created on 2008-06-29
Category: Health & Wellness
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Fenobarn FRAXA Research Leads to Orphan Drug Designation
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For the first time, a drug being developed for the treatment of
Fragile X has received an Orphan Drug Designation from the Food and Drug Administration (FDA).
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Memantine Treatment in Fragile X-Associated Tremor/Ataxia Syndrome
Clinical Trial
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Memantine Treatment in Fragile X-Associated Tremor/Ataxia Syndrome
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Fragile X syndrome partly cured in mice (ABC News in Science)
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Fragile X syndrome partly cured in mice
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Fragile X Syndrome May Be Caused By Two Duplicated Genes Producing Excess Protein
Dr Gecz says the duplicated genes - dubbed HSD17B10 and HUWE1 - produce excess protein, which appears to be the trigger leading to intellectual disability.
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Dr Gecz says the duplicated genes - dubbed HSD17B10 and HUWE1 - produce excess protein, which appears to be the trigger leading to intellectual disability.
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Mental retardation reversable in mice | Slevi
Could rapamycin offer the answer to mental retardation?
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Roche Eureka Moment on Disorder May Aid Autism Probe (Update1) - Bloomberg.com
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The first Fragile X medicine that targets the mGluR5
receptor may reach the market by 2011 or 2012
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FRAXA Research Foundation - finding a cure for Fragile X - Research
FRAXA's page on Fragile X Research
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Many faces of the same gene (ScienceAlert)
one in thirty or forty people from the general population is a carrier in the "grey" area. It's very common, and therefore even small clinical effects are borne by a great number of individuals.'
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