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@ARTICLE{Srulijes:139438,
author = {Srulijes, Karin and Brockmann, Kathrin and Ogbamicael,
Senait and Hobert, Markus A and Hauser, Ann-Kathrin and
Schulte, Claudia and Fritzen, Jasmin and Schwenk, Michael
and Gasser, Thomas and Berg, Daniela and Maetzler, Walter},
title = {{D}ual-{T}ask {P}erformance in {GBA} {P}arkinson's
{D}isease.},
journal = {Parkinson's disease},
volume = {2017},
issn = {2090-8083},
address = {London [u.a.]},
publisher = {Hindawi},
reportid = {DZNE-2020-05760},
pages = {8582740},
year = {2017},
abstract = {Parkinson's disease patients carrying a heterozygous
mutation in the gene glucocerebrosidase (GBA-PD) show faster
motor and cognitive decline than idiopathic Parkinson's
disease (iPD) patients, but the mechanisms behind this
observation are not well understood. Successful dual tasking
(DT) requires a smooth integration of motor and nonmotor
operations. This study compared the DT performances between
GBA-PD and iPD patients.Eleven GBA-PD patients (p.N370S,
p.L444P) and eleven matched iPD patients were included.
Clinical characterization included a motor score (Unified PD
Rating Scale-III, UPDRS-III) and nonmotor scores (Montreal
Cognitive Assessment, MoCA, and Beck's Depression
Inventory). Quantitative gait analysis during the
single-task (ST) and DT assessments was performed using a
wearable sensor unit. These parameters corrected for UPDRS
and MoCA were then compared between the groups.Under the DT
condition 'walking while checking boxes,' GBA-PD patients
showed slower gait and box-checking speeds than iPD
patients. GBA-PD and iPD patients did not show significant
differences regarding dual-task costs.This pilot study
suggests that DT performance with a secondary motor task is
worse in GBA-PD than in iPD patients. This finding may be
associated with the known enhanced motor and cognitive
deficits in GBA-PD compared to iPD and should motivate
further studies.},
cin = {AG Berg ; AG Berg / AG Gasser / AG Maetzler / Ext UKT},
ddc = {610},
cid = {I:(DE-2719)5000055 / I:(DE-2719)1210000 /
I:(DE-2719)5000024 / I:(DE-2719)5000058},
pnm = {345 - Population Studies and Genetics (POF3-345) / 344 -
Clinical and Health Care Research (POF3-344)},
pid = {G:(DE-HGF)POF3-345 / G:(DE-HGF)POF3-344},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:28819579},
pmc = {pmc:PMC5551514},
doi = {10.1155/2017/8582740},
url = {https://pub.dzne.de/record/139438},
}