The diagnostic utility of the new MDS criteria for multiple system atrophy: a retrospective autopsy cohort study
Objective: This study aimed to validate the clinical utility of the newly proposed criteria for multiple system atrophy (MSA) by the International Parkinson and Movement…Parkinson’s disease-specific cortical atrophy as an independent contributor to motor symptom in Parkinson’s disease
Objective: In this study, we identified specific pattern of cortical atrophy in Parkinson's disease (PD) and investigated whether PD-specific cortical atrophy contributed to motor symptom,…Smartphone App-Based Stroop Test as a surrogate for impaired self-awareness in Parkinson’s disease.
Objective: The aims of this study were to (i) develop age, sex and education stratified norm values of our smartphone app-based application of Stroop Test;…Clinical-based diagnosis and self-reported Parkinson’s disease in a population-based sample in southern Brazil
Objective: To report the frequency of self-reported PD and the diagnostic evaluation performed by clinical neurologists in a population-based cohort from south Brazil. Background: It…A forgotten cause of ocular motor apraxia
Objective: To report an example of the rare association between acquired hepatocerebral degeneration (AHD) and ocular motor apraxia (OA), and discuss its relevance for topical…Automatic Detection of Parkinson’s Disease by Voice Analysis
Objective: This study aimed to address this gap by investigating whether convolutional neural networks (CNN) can accurately distinguish PD patients from non-PD individuals. Background: Vocal…Comorbid Functional Neurologic disorders in patients with Parkinson.s disease in a rural hospital in Western part of India
Objective: To evaluate the prevalence and clinical profile of comorbid functional neurologic disorders (FNDs) among patients with Parkinson's disease (PD) in a rural medical teaching…Autosomal recessive Primary Familial Brain Calcification caused by MYORG mutations. Two unrelated cases from the south of Chile
Objective: To describe two unrelated cases of AR- PFBC with mutations in MYORG gene. Background: Primary Familial Brain Calcification (PFBC) is a rare neurogenetic disorder…Adult onset cerebrotendinous xanthomatosis (CTX) with parkinsonism responding to bilateral subthalamic nucleus deep brain stimulation
Objective: To describe a young male diagnosed with cerebrotendinous xanthomatosis who responded favourably to subthalamic nucleus deep brain stimulation (STN-DBS). Background: Cerebrotendinous Xanthomatosis is an…Cerebrospinal fluid biomarkers for diagnosis of Parkinson’s disease: a systematic review and network meta-analysis
Objective: In this study, we intended to use network meta-analysis to compare the diagnostic performances of different CSF biomarkers in the diagnosis and differential diagnosis…
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