Imaging-based Troubleshooting Deep Brain Stimulation in Parkinson’s Disease
Objective: Evaluate whether if electrodes reconstruction using Lead-DBS, an open source toolbox, in patients with Parkinson’s Disease (PwPDP) treated with Deep Brain Stimulation (DBS) presenting…Performance of a Smartphone-based Oculomotor Test as a Diagnostic Tool for Parkinson’s Disease
Objective: First, to ascertain whether a smartphone-based application measuring saccadic parameters can differentiate between patients with Parkinson’s disease (PD) and healthy controls (HC). Second, to…Acceptability of Digital Health Technologies in Early Parkinson’s Disease
Objective: The Wearable Assessments in the Clinic and at Home in PD (WATCH-PD) study is an observational, longitudinal study in early PD looking at disease…The Use of Biometric Feedback Devices for Stratification of Deep Brain Stimulation (DBS) Eligibility and Treatment Response in Parkinson Disease
Objective: To review the literature on digital biomarkers’ role in DBS candidacy assessment and treatment response in people with Parkinson Disease (PwP). Background: Visit frequency…Motor Onset of Parkinson’s disease: the proximal limbs are first
Objective: To determine if proximal body parts are more affected than distal body parts at the clinical onset of Parkinson’s disease (PD). Background: Motor features…A Benign Course of Parkinson’s Disease Associated with Different Mutations in the Glucocerebrosidase (GBA) Gene – a Case Series.
Objective: To describe a subtype of GBA-associated Parkinson's disease with a benign motor and cognitive course of disease. Background: Subjects carrying mutations in the GBA…Young-onset Parkinson’s disease in a female with pathogenic deletion of the PRRT2 gene
Objective: To report a novel case of young-onset Parksinon’s disease (YOPD) associated with a pathogenic deletion of the proline-rich transmembrane protein 2 gene (PRRT2). Background:…Engagement of the Black and African American Community in Parkinson’s Genetic Research
Objective: Increase racial diversity in Parkinson’s disease (PD) genetic research by engaging Black and African American people living with PD Background: Advancements in understanding the…Clinico-genetic profile of five patients with PARK-PINK1: A case series from India
Objective: The aim of our study is to describe the clinical features and genetic profile of patients of PARK-PINK1 and to draw correlation with genetic…A Rare Case of Parkinson’ s Disease Associated With Heterozygous ATP13A2 Gene Mutation: What If There Are No Atypical Features with a Later Onset?
Objective: Autosomal recessive mutations in ATP13A2 gene is a rare cause of levodopa-responsive parkinsonism with atypical features of supranuclear gaze palsy, spasticity, dystonia, dementia, myoclonus,…
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