Analysis of Depression and Suicidality Throughout the Course of Huntington Disease Using the Enroll-HD Registry
Objective: To describe the frequency of depression and suicidality among patients with Huntington disease (HD) stratified by HD stage and chorea severity. Background: High rates…Anosognosia in HD: Comparison of Self-report and Caregiver Ratings with Objective Performance Measures
Objective: Objective: To compare patient and caregiver report of cognitive, motoric, and psychiatric symptoms versus objective performance measures in patients with Huntington’s disease (HD). Background:…Olfactory dysfunction in patients with Huntington disease
Objective: To investigate olfactory dysfunction (OD) in individuals with Huntington disease (HD) and its relation to disease severity. Background: HD is a hereditary neurodegenerative disease…Profile and neural correlates of language disintegration in early Huntington’s disease
Objective: To explore the language profile of early Huntington's disease (HD) and the neural correlates that accompany the development of linguistic alterations in HD. Background:…Molecular diagnosis Approch for Huntington’s Disease in Tunisia
Objective: The aim of this study is to establish a molecular diagnosis approach for huntington's Disease (HD) Background: Huntington's disease (HD) is a rare and…A Useful Cognitive-Motor Dual Task Paradigm in Prodromal and Manifest HD
Objective: To investigate whether a cognitive-motor dual task (DT) paradigm uncovers deficits in balance in Huntington’s disease (HD) and, more importantly, prodromal HD, compared to…Feasibility of using ENROLL-HD for health services research: Evaluation of delays in Huntington’s Disease (HD) Diagnosis
Objective: To describe social and structural determinants of health of HD patients and to evaluate the feasibility of using this dataset for health services research.…Contemporary study of the difficulties of late diagnostics in patients with Huntington’s disease in Uzbekistan
Objective: To identify the causes that lead to late diagnosis of Huntington's disease. Background: Huntington's disease is a rare, progressive, and fatal autosomal dominant neurodegenerative…Cerebellar and other motor symptoms in Huntington’s Disease: A multiple scale correlation study
Objective: To describe the cerebellar symptoms and other accompanying movement disorders in Huntington's Disease (HD). Background: HD is a pathological entity whose etiological substrate is…Case of Chorea Hyperglycemia Basal Ganglia syndrome with normal glucose
Objective: To report a case of chorea hyperglycemia basal ganglia syndrome (CHBG) with normal glucose. Background: Elderly persons with CHBG usually have high glucose (average…
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