2018 International Congress Archives - Page 97 of 177

Longitudinal development of nigral iron load in Parkinson’s Disease

S. Franthal, L. Pirpamer, C. Rodler, N. Homayoon, M. Koegl, P. Katschnig-Winter, K. Wenzel, C. Langkammer, S. Ropele, R. Schmidt, P. Schwingenschuh (Graz, Austria)
Longitudinal follow-up of dual-lead thalamic deep brain stimulation for patients with treatment refractory multiple sclerosis tremor

B. Patel, R. Barmore, A. Elkouzi, P. Zeilman, X. Bai, L. Almeida, K. Foote, M. Okun (Gainesville, FL, USA)
Longitudinal MRI to predict cognitive impairment in Parkinson’s disease

T. Melzer, D. Myall, L. Livingston, M. Almuqbel, M. MacAskill, T. Pitcher, K. Horne, S. Grenfell, M. Pascoe, D. Miller, R. Keenan, J. Dalrymple-Alford, T. Anderson (Christchurch, New Zealand)
Longitudinal observational study on late onset Parkinson’s disease over a decade

S. Raha, L. Ebenezer (Bridgend, United Kingdom)
Loss of paraplegin drives spasticity rather than ataxia in SPG7: A European cohort analysis of 238 patients

G. Coarelli, R. Schule, B. vande Warrenburg, P. de Jonghe, C. Ewenczyk, A. Martinuzzi, M. Synofzik, E. Hamer, J. Baets, M. Anheim, L. Schöls, T. Deconinck, B. Fontaine, T. Klockgether, MG. D'Angelo, ML. Monin, P. Charles, MT. Bassi, T. Klopstock, E. Ollagnon-Roman, C. Kamm, M. Papin, CS. Davoine, G. Banneau, S. Tezenasdu Montcel, D. Seilhean, A. Brice, C. Duyckaerts, G. Stevanin, A. Durr (Paris, France)
Loss of VPS29 disrupts retromer function and synaptic transmission, leading to neurodegeneration in Drosophila

H. Ye, D. Li-Kroeger, Y. Li, H. Bellen, J. Shulman (Houston, TX, USA)
Lottery choice task as a detect tool for PD patients with pathological gambling

W. Liu, R. Wu, J. Goh (Hualien, Taiwan)
Low body weight is associated with poor functional status in Parkinson’s disease (PD)

HF. Chan, N. Cheung, D. Chau, CW. Woo, B. Chee, A. Leung, S. Or, WC. Fong (Hong Kong)
Low-Fat Versus Ketogenic Diet In Parkinson’s Disease: A Pilot Randomized Controlled Trial

M. Phillips, D. Murtagh, L. Gilbertson, F. Asztely, C. Lynch (Hamilton, New Zealand)
LRRK2 and GBA genetic mutations are not uncommon in an unselected Ashkenazi elderly cohort with PD

S. Isaacson, J. Isaacson (Boca Raton, FL, USA)