第59回日本神経学会学術大会

講演情報

神経疾患の克服を目指して

[OC-02] Research frontline of hereditary cerebellar ataxias

2018年5月23日(水) 13:20 〜 15:10 第10会場 (ロイトン札幌2F ハイネス・ホール)

座長:池田 佳生(群馬大学大学院医学系研究科脳神経内科学), 髙橋 祐二(国立精神・神経医療研究センター神経内科)

[OC-02-2] Repeat associated Non-AUG initiated (RAN) translation in Fragile X-associated Tremor Ataxia Syndrome

Peter K. Todd (University of Michigan)

Peter K. Todd, M.D., Ph.D., is the Bucky and Patti Harris Collegiate Professor of Neurology at the University of Michigan. Dr. Todd completed his MD and PhD at the University of Wisconsin, his Neurology Residency at the University of Pennsylvania and research intensive fellowship in movement disorders and neurogenetics at the University of Michigan under the tutelage of Dr. Henry Paulson. Dr. Todd’s research focuses on neurological disorders that result from nucleotide repeat expansions. His lab aims to define the pathogenic mechanisms by which these repeat expansions elicit human diseases such as ALS and Fragile X-associated disorders and develop therapeutics for those conditions based on these insights. His group has made significant contributions to this research field by defining a novel mechanism by which repeats cause disease through aberrant protein translation- a process known as “RAN Translation”. He has won numerous awards, including the S. Weir Mitchell Award from the American Academy of Neurology, the Hagerman Research Prize from the National Fragile X Foundation, and the Basic Science Research Award from the University Of Michigan School Of Medicine. Clinically, Dr. Todd co-directs the Michigan Fragile X and Ataxia Clinics and is inaugural director of the Michigan Neurogenetics Clinical Research Program.

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