2019 International Congress Archives - Page 25 of 217

Associations of gait disorders and future falls in the elderly: a prospective population-based study

K. Marini, P. Mahlknecht, O. Schorr, M. Baumgartner, A. Djamshidian, A. Gasperi, S. Kiechl, G. Rungger, H. Stockner, J. Willeit, W. Poewe, K. Seppi (Innsbruck, Austria)
Associations of Genetic, Epigenetic and Phenotypic Measures in the Dominican Republic PKAN Cohort

F. Middleton, A. Espinoza, D. Larocca, R. Ericson, M. Santana Jimenez, K. Wagner, P. Stoeter, C. Bass, C. Muniz, S. Baser (Pittsburgh, PA, USA)
Associations of microtubule associated protein tau (MAPT) H1 subhaplotypes and the MAPT H2 haplotype with demographic and clinical features in Parkinson`s disease

A. Deutschlander, M. Heckman, T. Konno, M. Ossi, N. Diehl, A. Soto, A. Strongosky, R. Uitti, J. van Gerpen, O. Ross, W. Zbigniew (Jacksonville, FL, USA)
Asymmetrical striatal dopamine transporter binding correlates with excess contralateral rest tremor

A. Fois, F. Chang, R. Barnett, K. London, N. Mahant, A. Ha, Z. Aldaajani, B. Cruse, H. Morales-Briceno, K. Ma, V. Fung (Dhahran, Saudi Arabia)
Asymmetry of motor symptoms in patients with Parkinson’s Disease

Y. Trufanov, N. Svyrydova, V. Svistun, I. Harkava, H. Bondarenko, N. Zhhilova (Kyiv, Ukraine)
Ataxia by Mutation in CACNA1A Gene – Case Series

P. Almeida, J. Pedroso, I. Brandi (Salvador, Brazil)
Ataxia with(out) oculomotor apraxia: A unique SETX mutation in 3 siblings

P. Khemani, A. Kuhlman, B. Bulica, N. Patel (Seattle, WA, USA)
Ataxin-2 gene in the Cuban population: Mutagenesis and epigenetic DNA methylation disease influencing phenotype

J. Laffita-Mesa, L. Velazquez Perez (Stockholm, Sweden)
ATP1A3 Gene Mutations Associated With Rapid-Onset Dystonia-Parkinsonism (RDP) Presenting As Functional Neurologic Disorder: A Report of Two Cases

T. Biller, R. Chuang, S. Ro (Seattle, WA, USA)
Atropine as Alternate Therapy for Treatment of Sialorrhea in Parksinson’s Disease

K. Papesh, J. Nguyen (Las Vegas, NV, USA)