Juvenile Huntington’s Disease in Tunisia: Clinical Diversity and Literature review
Objective: We conducted the first JHD clinical and molecular features in Tunisia and North Africa, contributing to better understanding the diverse manifestation of the disease…Cognitive profiling in a cohort of Huntington’s disease (HD) patients
Objective: To define neuropsychological profile of HD patients adopting Parkinson’s disease Level II criteria for cognitive diagnosis[1]. Background: HD is a rare autosomal dominant genetic…Mimics or multiplicity: two patients with a PSP phenotype and underlying genetic neurodegenerative disorders.
Objective: To describe a two cases of patients presenting with a PSP phenotype and genetic findings consisted with Huntington’s disease (HD) in one case and…Nocturnal attacks of abnormal sleep behaviors and abnormal movements induced by insulin: A case report
Objective: To report a case of abnormal sleep behavior associated with hypoglycemia induced by insulin. Background: Hypoglycemia is a serious condition that can be manifested…Speech markers of Presymptomatic and Prodromal Huntington’s disease
Objective: To investigate the sensitivity of digital speech measures for detecting subtle cognitive-linguistic and fine motor features in people carrying the expanded HD gene, with…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…
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