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Recent media reports have raised concerns about
the impact of the new diagnostic criteria for autism spectrum disorders. Learn more...
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Highlighted Article: Pathogenesis of lethal cardiac
arrhythmias in mecp2 mutant mice: implication for therapy in Rett syndrome. Read full abstract...
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Highlighted Article: What does the nature of the
MECP2 mutation tell us about parental origin and recurrence risk in Rett syndrome? Read the full abstract...
RettSearch is an international, multi-center
collaborative network of clinically-oriented researchers. Its mission is to promote the
development of new therapeutic approaches for Rett syndrome (RTT) by collecting information and
pursuing research in areas of relevance to clinical trials in RTT. Under the leadership of the
Executive Committee - Sarojini Budden, M.D., FRCPC; John Christodoulou, , F.R.A.C.P., Ph.D.,
A.R.C.P.A..; Daniel Glaze, M.D.; Helen Leonard, M.B.Ch.B., M.P.H.;Jeff Neul, M.D.; Carolyn
Schanen, M.D.; Francesca Mari, M.D., Ph.D; and Walter Kaufmann, M.D. (Chair) - members are
grouped into committees or "working groups," each with a specific theme and task. Clinical
researchers interested in applying for membership should send a current CV to the RettSearch Coordinator. Learn more about our History/Mission and Expected
Outcomes. |
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InterRett:
The Value of International Data Learn more... |
RettBase
The IRSF MECP2 Variation DatabaseRettBASE aims to provide a list of all published MECP2 gene variations (including polymorphisms), whereby unpublished data can be submitted and made available to all researchers. Learn more...
News & Publications
Highlighted article: Rett networked database: An integrated clinical and genetic network of rett syndrome databases. Read full abstract...
Highlighted article: Early speech-language development in females with Rett syndrome: focusing on the preserved speech variant. Read full abstract...
Links to NIH Funding
Resources
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| Consider applying for a RettSearch microgrant! |
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