Cumulative Real-World Experience with Deutetrabenazine for Huntington’s Disease Chorea at a Single Center of Excellence in the US
Objective: To summarize clinical experience and outcomes with deutetrabenazine (DTBZ) as a treatment for Huntington’s disease (HD) chorea from the Huntington’s Disease Society of America…Visual cognition differences between asymptomatic and symptomatic carriers of Huntington’s disease (HD)
Objective: This study aims to analyze the visual cognition profile of asymptomatic and symptomatic carriers of Huntington's disease (HD), compared with healthy controls (HC), and…Impaired saccadic inhibition in Huntington mutation carriers
Objective: To assess saccadic paradigms in asymptomatic Huntington disease mutation carriers. Background: Huntington’s disease (HD) is characterized by motor, cognitive and behavioural abnormalities, such as…Akinetic-rigid motor presentation among adult-onset HD participants in Enroll-HD
Objective: To characterize a variant of adult Huntington’s disease (HD) with akinetic-rigid syndrome (ARS) as initial motor manifestation Background: HD Cases have been reported with…Brain MRI Cortical Atrophy correlation to clinical onset in Huntington’s Disease
Objective: To describe brain Magnetic Resonance Imaging (MRI) characteristics in Latin American individuals with Huntington's Disease (HD) and to correlate them to major symptom at…New-onset movement disorders in patients with COVID-19 from two centers in Western India
Objective: To study the frequency and characteristics of movement disorders in patients with COVID-19 at two tertiary-care hospitals in Western India. Background: As of March…Characterising the incidence of comorbidities, hospitalisations, and death in patients diagnosed with Huntington’s disease: A cohort study of linked Swedish National Registries (2002-2019)
Objective: To investigate comorbidities, hospitalizations, and mortality in patients newly diagnosed with Huntington’s disease using data extracted from three linked Swedish national health registries from…A case of Bainbridge-Ropers syndrome in a child.
Objective: This study describe the clinical case of Bainbridge-Ropers syndrome caused by the ASXL3 gene mutation. Background: Bainbridge-Ropers syndrome is an autosomal dominant disorder typically…Diabetes Mellitus in Huntington’s disease. The Argentinean perspective
Objective: to compare the prevalence of diabetes mellitus (DM) in a self-reported series of local Huntington disease (HD) participants in the ENROLL-HD registry with the…Evaluation of Health-Related Quality of Life for Individuals with Huntington’s Disease and Care Partners in Canada
Objective: To evaluate the impact of Huntington’s disease (HD) on health-related quality of life (HRQoL) for individuals with HD and care partners in Canada. Background:…
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