MDS Virtual Congress 2021 Archives - Page 25 of 132

Clinical correlates of visual hallucinations in Parkinson’s disease

G. Mandic Stojmenovic, T. Stojkovic, E. Stefanova, V. Markovic, I. Stankovic Tutus, I. Petrovic, N. Dragasevic Miskovic, M. Svetel, V. Kostic (Belgrade, Serbia)
Clinical epidemiology of movement disorders in Douala General Hospital, Cameroon: A two years retrospective study

D. Gams Massi, AM. Magnerou, G. Tchumno Mayoue, EA. Babe, NY. Mapoure (Douala, Cameroon)
Clinical Features Associated with Dysautonomia in Prodromal Parkinson’s Disease

C. Miller-Patterson, J. Hsu, J. Morley, A. Siderowf, A. Willis (Philadelphia, USA)
Clinical heterogeneity of DYT-KMT2B mutation in a family with monozygotic twins

O. Mcwilliam, C. Fagerberg, M. Larsen, D. Kondiziella, I. Havsteen, A. Løkkegaard (Copenhagen N, Denmark)
Clinical Outcomes in Parkinson’s with COVID 19 during the’ first wave’ in West Berkshire, United Kingdom (UK)

M. Khwaja, A. Chatterjee, N. Butt, N. Virgincar, M. Todd, T. Nanayakkara, G. Pun (Reading, United Kingdom)
Clinical phenotype and biomarkers in sporadic degenerative ataxia: longitudinal data from the SPORTAX registry

D. önder, C. Wilke, J. Faber, T. Schaprian, I. Giordano, M. Grobe-Einsler, L. Schöls, S. Vielhaber, J. Machts, C. Kamm, A. Dudesek, T. Klopstock, C. Stendel, D. Timmann-Braun, S. Boesch, A. Eigentler, B. van Dewarrenburg, J. van Gaalen, C. Tallaksen, I. Wedding, A. Filla, G. Silvestri, M. Masciullo, C. Ganos, J. Kang, D. Sarah, M. Synofzik, T. Klockgether (Bonn, Germany)
Clinical predictors of impulsive and compulsive behavior after subthalamic stimulation in Parkinson’s disease

A. Sauerbier, P. Loehrer, S. Jost, S. Heil, J. Petry-Schmelzer, J. Herberg, P. Bachon, S. Aloui, A. Gronostay, L. Klingelhoefer, J. Baldermann, D. Huys, C. Nimsky, M. Barbe, G. Fink, P. Martinez-Martin, K. Chaudhuri, V. Visser-Vandewalle, L. Timmermann, D. Weintraub, H. Dafsari (Cologne, Germany)
Clinical presentation of coexistence of Spinocerebellar ataxia (SCA14) gene duplication variant in association with Spinocerebellar Ataxia (SCA8) gene mutation in a same patient.

A. Ahmed (Winter Park, USA)
Clinical presentation of Wilson’s disease in pediatric and adult patients: A systematic review

A. Rochel-Pérez, K. Santos-Zaldivar, O. Cuevas-Koh, M. Azuela-Morales, N. Méndez-Domínguez (Mérida, Mexico)
Clinical profile and treatment outcomes of inherited hypermanganesemia among 27 Indian children: A retrospective multi-centric study

D. Garg, S. Yoganathan, A. Saini, N. Sankhyan, U. Kalane, K. Srivastava, A. Bothre, D. Panigrahi, M. Kamate, M. Juneja, V. Udani, S. Sharma (Delhi, India)