Smartphone-based context awareness to improve ambulatory Parkinson’s monitoring
Objective: To determine the utility of context-awareness algorithms based on sensors in smartphones to improve ambulatory Parkinson’s disease (PD) monitoring. Background: Previous research shows that optimal motion sensor-based ambulatory PD monitoring requires multiple sensors to…Clinical and kinematic assessment of a glove-based tremor dampener in patients with essential tremor
Objective: To determine the effectiveness of a biomechanical glove in the setting of essential tremor (ET) using both kinematic and clinical evaluation. Background: Essential tremor…The Unique Voiceprint Changed In Parkinson’s Disease
Objective: To discover the unique voiceprint changed in patients with Parkinson’s disease. Background: Parkinson’s disease, PD, is a serious neurodegenerative disease affected millions old people…Intravenous Immunoglobulin Treatment did not improve Tics in a Patient with Gilles de la Tourette Syndrome and intrathecal Antibody Synthesis
Objective: Here we present the unique case of a female patient with GTS, who not only exhibited intrathecal antibody synthesis documented by positive OCBs, but…Altered Spontaneous Brain Activity in Essential Tremor with and without Resting Tremor: A Resting-state fMRI Study
Objective: This study aims to use resting-state functional magnetic resonance imaging (rs-fMRI) to explore the alterations of brain activity in drug-naïve patients with Essential tremor…Botulinum Toxin Injections for Upper Limb Dystonia with Tremor
Objective: To study the effect of BoNT injections on tremor in patients with upper limb dystonia with hand tremor. Background: Tremor is a common accompaniment…Creating National Competencies in Physical Activity for Exercise Professionals Working with People with Parkinson’s Disease
Objective: On March 5-6th 2020, the Parkinson’s Foundation is convening a meeting to assemble thought leaders in physical activity and education for Parkinson’s disease. Our…CAPN1 mutations are more common than expected in patients with hereditary spastic paraparesis
Objective: To report 4 families with hereditary spastic paraparesis due to CAPN1 mutations. Background: Some years ago, CAPN1 mutations have been described as a cause…Novel Mutation in the Protein Kinase C Gamma Gene Causing Spinocerebellar Ataxia-14 in a Large Family
Objective: To report a novel mutation not been previously reported in large, multi-ethnic general populations, in the protein kinase C gamma (PRKCG) gene causing spinocerebellar ataxia…Clinical and genetic abnormalities in patients with Friedreich’s ataxia: A genotype-phenotype correlation
Objective: To examine the possibility of molecular finding affecting FRDA phenotype, we studied the clinical features and ascertained the GAA repeat sizes in FRDA patients…
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