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Capture d’écran 2015-07-31 à 15.09.19

Please help maintaining the Rett Syndrome Database Network

Dear friends, As President of Rett Syndrome Europe, I am writing to you today to ask for your Association’s support for the European Rett database located in Italy: the Rett Syndrome Database Network (RSDN). The simple fact is that vital research on Rett syndrome or clinical trials cannot be easily achieved without collecting and analysing […]

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A research consortium against RETT syndrome

PRESS RELEASE Milan, December 3, 2013 – It was held at the headquarters of the IRCCS – Istituto di Ricerche Mario Negri in Milan, the first operational meeting dell’AIRETT RESEARCH TEAM Consortium created by renowned Italian research institutes that are involved in a joint effort to study Rett Syndrome, a rare disease, little known to the general public, for […]

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For Clinicians and Scientists : Rett Syndrome Networked Database

Rett Syndrome Networked Database is a tool of great value to both the scientific and the clinical RTT community More : www.rettdatabasenetwork.org and download PDF

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The 2012 World Rett Syndrome Congress

The 2012 World Rett Syndrome Congress, hosted for the first time in the United States, is a prestigious global meeting, attended by the world’s leading researchers, clinicians and educators in the field of Rett syndrome. It will consist of 4 distinct, yet interconnected meetings June 22-26, 2012: This dynamic program will help chart the course […]

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