2017 International Congress

June 4-8, 2017. Vancouver, BC.

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Whole Exome Sequencing (WES) identifies a TUBB4A Mutation in two Saudi siblings with hypomyelinating leukodystrophy associated with atrophy of basal ganglia and cerebellum.

Z. Aldaajani, E.-S. Ali (Dhahran, Saudi Arabia)
Whole exome sequencing in essential tremor.

I. Alfradique-Dunham, L. Robak, A. Kaw, O. Fagbongbe, Z. Coban Akdemir, E. Young, J. Lupski, J. Jankovic, J. Shulman (Houston, TX, USA)
WILSON’S DISEASE: A Mongolian case

U. Dashdorj, S. Jambal (Ulaanbaatar 51, Mongolia)
Writing training enhances neural connectivity in Parkinson’s patients with micrographia

E. Nackaerts, J. Michely, E. Heremans, S. Swinnen, B. Smits-Engelsmans, W. Vandenberghe, C. Grefkes, A. Nieuwboer (Leuven, Belgium)
WTX101 – A Novel Copper Modulating Agent for Wilson Disease Demonstrates Efficacy and Safety in a Phase 2, Multi-Center, Open Label Study

D. Bega, A. Ala, F. Askari, J. Bronstein, A. Czlonkowska, P. Ferenci, D. Nicholl, K.-H. Weiss, M. Schilsky (Chicago, IL, USA)
Young Onset Parkinson’s Disease (YOPD): A different disease entity?

H. Chan, Y. Cheung, D. Chau, V. Lo, C. Woo, S. Tse, T. Fung, A. Leung, W. Fong (Hong Kong, Hong Kong)
α-Synuclein Preformed Fibrils Induce Disruption of Myelin Basic Protein Expression in Primary Oligodendrocyte Culture; Deciphering Glial Pathology in Multiple System Atrophy

S. Kaji, T. Maki, N. Uemura, R. Takahashi (Kyoto, Japan)
Сase of myotonic dystrophy

A. Jusupova (Bishkek, Kyrgyzstan)

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