Analysing an extension type of Parkinson’s disease
Objective: We analyse an extension type of Parkinson’s disease. Background: At the International Congress of the Movement Disorder Society last year, we reviewed a patient…First Scientific Description of the Hepato-Lenticular Degeneration
Objective: Hepato-Lenticular Degeneration (HLD) first described by German pathologist Friedrich Theodor von Frerichs in 1854, but in the West it called Wilson's Disease. In Russia…Sleep and Polysomnographic Abnormalities in Indian Patients with Huntington’s Disease
Objective: To study the sleep abnormalities in patients with HD by usingquestionnaire and Video Polysomnography (VPSG) and correlate with the eye movement abnormalities. Background: About 87.8% of the patients report some sleep disturbance…Huntington’s Disease in Israel – 20 years of follow up from Maccabi Healthcare Services
Objective: To describe Huntington’s Disease (HD) epidemiology in Israel and depict comorbidities and longitudinal healthcare resources utilization. Background: HD is a rare, inherited neurodegenerative disorder,…HD Constellation: A novel patient-centred approach to enriching clinical datasets by combining medical record chart review and Enroll-HD
Objective: HD Constellation aims to create a dataset providing a longitudinal view of the Huntington’s disease (HD) course, based on physician-provided medical records in the…Longitudinal Utility of the Montreal Cognitive Assessment and Mini Mental State Exam in Huntington’s disease (HD)
Objective: Neuropsychological assessments are useful tools for examining and tracking cognitive impairment in individuals with neurological disorders; however, a full neuropsychological battery is not realistic…Performance at the Category-Exemplars language test (CATEX) in Parkinson’s disease and Huntington’s disease Italian population
Objective: This study aims to explore CATEX sensitivity to detect early cognitive deficits in Huntington’s disease (HD) and Parkinson’s disease (PD) Italian population. Background: PD…Genetic analysis of Huntington’s Disease in a Brazilian Amazonian population
Objective: Characterize genetically a series of cases of patients with Huntington’s disease and their family members at risk in the city of Manaus, capital of…Can Handwriting Movement Abnormalities Serve as an Early Biomarker of Transition to Manifest Huntington’s disease?
Objective: The objective of this study was to examine whether handwriting abnormalities are present prior to clinically manifest chorea in Huntington's disease (HD) and can…Modelling Huntington’s disease diagnosed prevalence from diagnosed incidence and survival time
Objective: To develop an epidemiological model of manifest Huntington’s disease (HD) to estimate international HD diagnosed prevalence by Shoulson–Fahn Total Functional Capacity (TFC)-based Stage based…
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