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Rett Syndrome Research Trust NYC Journal

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A digital version of the journal created for the 4th Annual Reverse Rett NYC event which took place November 8, 2012 at The Broad Street Ballroom in Manhattan.

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The Rett Syndrome Research Trust is a non-profit exclusively devoted to global research on Rett Syndrome and related MECP2 disorders. Our goal is to heal children and adults who will otherwise suffer the effects of these disorders for the rest of their lives. Subscribe for updates on Rett Syndrome and The Rett Syndrome Research Trust at http://bit.ly/reverserett

Reverse Rett in London with Professor Adrian Bird, 2011 | Rett Syndrome Research Trust

Interview with Monica Justice, PhD | Rett Syndrome Research Trust

Rett Syndrome: The Possibilities with Monica Coenraads of RSRT and Rachael Bloom of RSRT UK

Effective Gene Therapy Treatment In Mice | Rett Syndrome Research Trust

Polish Rett Syndrome Association on January 13, 2021 Rett Syndrome Research Trust

Assessing Rett Symptoms with Cutting Edge Biosensors and Invisible Technology | RSRT

Town Hall: When will there be a cure for Rett syndrome? | Rett Syndrome Research Trist

An Update on the New Rett Digital Natural History Study | Rett Syndrome Research Trust

Interview with Skirmantas Kriaucionis, PhD | Rett Syndrome Research Trust

Rett Syndrome \ Hope for Hannah

RNA Editing and Its Potential to Improve Rett Syndrome Symptoms | Rett Syndrome Research Trust

Ben Philpot: Gene Awakenings for the Treatment of Neurological Disorders | RSRT

Interview with David Katz | Rett Syndrome Research Trust

Rett Syndrome Must Knows: Diagnosis, Symptoms, History and Care

Michael Green Shares The State of His Research | Rett Syndrome Research Trust

A Conversation with Neurogene's Leadership | Rett Syndrome Research Trust

Hope for Hannah & Gaby | Rett Syndrome Research Trust

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