The impact of biographic factors and lifestyle on the symptoms of Parkinson’s Disease – a five year follow-up
Objective: To identify biographic parameters that may have an impact on the different symptoms of parkinson’s disease. Background: Parkinson’s disease (PD) is a neurodegenerative movement…Association between Parkinson’s Disease and Atrial Fibrillation: A Literature Review
Objective: Our literature review aims to summarize what has been reported in the literature with the next steps of looking at Kaiser Permanente (KP) to…Caveats regarding a family with PD and LRRK2 mutations
Objective: To describe and discuss genetic considerations regarding a kindred with PD cases with similar clinical characteristics, some with identified mutations in the LRRK2 gene…Development and Validation of an Algorithm to Automatically Assess Motor Symptoms of Parkinson’s Disease
Objective: To assist non-specialists in evaluating patients with advanced Parkinson's disease who have difficulty visiting specialists’ hospitals, we developed an algorithm to automatically rate the…Prodromal dementia with Lewy bodies in REM sleep behavior disorder: A multicenter study
Objective: To assess the progression and predictive value of neuropsychological testing on the development of dementia in idiopathic REM sleep behavior disorder (iRBD). Background: iRBD…A 20-year review of a Movement Disorders Database in Singapore
Objective: To conduct a 20-year review of the movement disorders (MD) clinical database in Singapore. Background: MDs contribute to a significant portion of chronic disease…DNAJC12 defect a new neurodevelopmental disorder associated with parkinsonism-dystonia
Objective: to expand the phenotypic characterization of this rare disorder, clinical presentation and outcome of a cohort of patients affected DNAJC12 defect are reported. Background:…Dopamine-responsive x-linked parkinsonism-epilepsy due to phosphoglycerate kinase-1 deficiency
Objective: To describe the phenotype of three siblings with early-onset parkinsonism and epilepsy due to an x-linked phosphoglycerate kinase 1 deficiency, expanding our understanding of…Phenotype and brain [18F] FDG patterns in patients with freezing of gait as the main clinical feature
Objective: To describe the clinical phenotype and brain [18F] FDG patterns in 52 patients exhibiting freezing of gait and/or gait instability as the main clinical…Prevalence of seizures in patients with Neurodegeneration with Brain Iron Accumulation
Objective: To investigate the frequency and pattern of seizures in Neurodegeneration with brain iron accumulation (NBIA) disorders in a South Indian cohort. Background: Seizure as…
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