MDS Virtual Congress 2020 Archives - Page 95 of 149

Non-Staged Bilateral GPi DBS Lead Revision Using iMRI: A Case Report

B. Hwang, D. Mampre, K. Mills, A. Butala, W. Anderson (Baltimore, MD, USA)
Noninvasive brain stimulation to treat hypokinetic dysarthria in PD: A sham stimulation-controlled trial

I. Rektorova, L. Brabenec, P. Klobusiakova, M. Kostalova (Brno, Czech Republic)
Noradrenergic terminal and locus coeruleus cell loss may be uncoupled in Parkinson’s disease – a PET and MRI multi-modal imaging study

M. Kinnerup, C. Doppler, E. Farrher, T. Fedorova, J. Schaldemose, K. Knudsen, R. Isamail, A. Hansen, K. Stær, G. Fink, J. Shah, D. Brooks, A. Nahimi, P. Borghammer, M. Sommerauer (Aarhus, Denmark)
Normative vs. patient-specific brain connectivity in Deep Brain Stimulation

Q. Wang, H. Akram, M. Muthuraman, G. Gonzalez-Escamilla, S. A. Sheth, G. Groppa, N. Vanegas-Arroyave, L. Zrinzo, N. Li, A. Kühn, A. Horn (Berlin, Germany)
Northwestern University Feinberg School of Medicine Parkinson’s disease and Movement Disorders Center Biorepository: bringing the clinic and lab together

A. Hernandez, S. Lubbe, T. Simuni, D. Bega, D. Krainc, N. Mencacci, R. Modiest, P. Opal, C. Taylor, N. Shetty, R. Malkani, J. Blackburn (Chicago, IL, USA)
Not so simple: the challenge of developing a non-motor symptoms app (NMS Assist) for people with Parkinson’s (PwP)

T. Gorst, T. Dominey, J. Whipps, S. Whipps, J. Cooke, S. Mullin, I. Maramba, E. Edwards, C. Carroll (Plymouth, United Kingdom)
Novel Dentato-Olivo-Luysian Atrophy in a Greek Family

S. Alshimemeri, K. Yoshida, N. Visanji, E. Rogaeva, R. Munhoz, E. Slow, A. Lang, G. Kovacs (Toronto, ON, Canada)
Novel GNO1 mutation in monozygotic twins responsive to DBS

B. Bulica (West Bloomfield, MI, USA)
Novel KCND3 mutation associated with paroxysmal motor exacerbations in spinocerebellar ataxia 19

M. Paucar, R. Ågren, T. Li, S. Lissmats, Å. Bergendal, I. Savitcheva, D. Nilsson, K. Sahlholm, P. Svenningsson, J. Nilsson (Stockholm, Sweden)
Novel Mutation in the Protein Kinase C Gamma Gene Causing Spinocerebellar Ataxia-14 in a Large Family

J. Lahrmann, M. Dagostine, D. Machado (Cheshire, CT, USA)