Impact of DBS STN on motor symptoms, postural instability, QoL in PD patients from the Belarusian population
Objective: To evaluate the efficiency of DBS STN in PD patients in Republican center of neurology and neurosurgery Background: Deep brain stimulation (DBS) of the…Advancing Interpretability in Parkinson’s Disease Voice Analysis: A Multilingual AI Approach
Objective: This study aims to advance the interpretability of machine learning (ML) models in the detection of Parkinson's Disease (PD) through a novel approach analyzing…AI-Powered Eyewear for Routine Facial Expression Analysis in Parkinson’s Disease: Study design and goals
Objective: Collect routine facial expression data from people with Parkinson’s Disease (PwP) and healthy controls via user-friendly AI-powered eyewear and develop AI algorithms to distinguish…Pressure Sensor Insole Gait Assessment for Parkinson’s Disease patients: A longitudinal study.
Objective: To evaluate a computational analysis of gait, based on pressure sensors insoles data, by correlating it with clinical assessments of motor symptoms in Parkinson's…Disrupted Sleep Circadian Rhythms and Brain Disorders: A Large Prospective Cohort Study
Objective: Disrupted sleep circadian rhythms have been linked to increased risks of dementia and mental health, but their associations with other brain disorders were underestimated.…Prevalence of Parkinson’s Disease and Possible Parkinsonian Syndrome in Gaucher Disease: Data From the ICGG Gaucher Registry
Objective: To estimate the age-specific risk of Parkinson’s disease (PD) and possible parkinsonian syndrome (pPS) in Gaucher disease (GD) based on registry data. Background: While…Exploring MAPT Haplotypes in Parkinson’s Disease in a Diverse Cohort: Insights from the Global Parkinson’s Genetics Program
Objective: To assess the frequency of H1/H2 haplotypes in MAPT across diverse ancestries from the Global Parkinson’s Genetics Program(GP2) and investigate their association with Parkinson's…Studying monogenic Parkinson’s disease by building a global cohort of mutation carriers
Objective: ObjectiveTo build a multi-ancestry cohort of individuals with pathogenic variants in genes known to cause Parkinson’s disease (PD) to study monogenic PD at a…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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