September 3, 2023

Dr. Michael Zech Receives the David Marsden Award 2023

Our congratulations to Dr. Michael Zech, from the Institute of Human Genetics, Technical University of Munich and the Institute of Neurogenomics, Helmholtz Zentrum München, in Munich, Germany and the David Marsden Award 2023 for his paper: Biallelic AOPEP Loss-of-Function Variants Cause Progressive Dystonia with Prominent Limb Involvement. Last July Dr. Zech was presented with the…

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September 20, 2022

Presentation of the DMA at the EAN 2022 Basal Ganglia Club Session

European Academy of Neurology is a non-profit, independent organisation representing more than 45,000 members, as well as 47 European national societies. The 8th Congress of the EAN took place in Vienna in June this year. EAN Congress is one of the biggest neurological events in Europe. This year 380 lecturers and 5300 onsite participants took…

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June 15, 2022

David Marsden Award Winner Dr Susanne Knorr

At the end of Dystonia Europe’s annual conference Dystonia Days, President Adam Kalinowski presented the David Marsden Award to Dr Susanne Knorr from the University Hospital in Würzburg Germany, coincidentally the same place that last year’s winner was from. Susanne then went on to present her research ‘The evolution of dystonia-like movements in TOR1A rats after…

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May 30, 2022

Winner of the David Marsden Award 2022 Dr. Susanne Knorr

Susanne Knorr, Senior Consultant Neurologist and Researcher Würzburg University Hospital. Photo by Stephan Röhl Our congratulations to Dr. Susanne Knorr, department  of Neurology, University Hospital of Würzburg, Germany and the David Marsden Award 2022 winner for her paper: “The evolution of dystonia-like movements in TOR1A rats after transient nerve injury is accompanied by dopaminergic dysregulation and…

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May 30, 2022

Prof. Tom Warner, Queen Square London: About the Research of Dr. Susanne Knorr, the David Marsden Award Winner 2022

The changes in the brain that lead to dystonic movements have been the subject of extensive investigation, particularly for the genetic forms. DYT1 dystonia is the commonest genetic cause of childhood onset dystonia and various studies in cell, animal and human studies suggest it is due to a problem with circuits controlling movement, focused on…

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