Widespread White Matter Changes in Manifest Huntington’s Disease
Objective: To characterize white matter changes in Huntington’s Disease (HD). Background: HD is a genetic neurodegenerative disorder characterized by motor, cognitive, and psychiatric symptoms. Diffusion Tensor…Hyperkinetic Movement Disorder associated with Papillary Thyroid Carcinoma
Objective: To describe a case of hyperkinetic movement disorder associated with papillary thyroid carcinoma, highlighting the diagnostic workup and therapeutic interventions. Background: Paraneoplastic neurological syndromes…Huntington’s Disease: Overview from 20 Years of a Single-Center Experience
Objective: This study evaluates patient data from individuals with Huntington’s disease who attended our single tertiary center. Background: Huntington’s disease is an inherited neurodegenerative disorder…Blood-based somatic CAG repeat expansion and clinical progression in Huntington’s disease patients from Western China
Objective: To investigate the association between blood-based somatic CAG repeat expansion ratio (SER) and clinical characteristics in Huntington’s disease (HD) patients from Western China. Background:…The Unlikely Treatable A Case of Ataxia
Objective: To present the first reported Colombian case in a patient presenting COQ8A-ataxia with bilateral palpebral ptosis, who had a favorable response to CoQ10 supplementation…Safety and Efficacy of a Wrist-Worn Vibratory Stimulator for Upper Limb Tremor Reduction in Essential Tremor (ULTRE): A Randomized, Controlled Trial
Objective: To assess the safety, tolerability, and efficacy of a wrist-worn vibratory stimulator by comparing two active paradigms (Pulsed (AP), Continuous (AC)) to Sham in…Effects of transcutaneous periodic vibratory stimulation on gait and balance function in Spinocerebellar degeneration -a pilot study
Objective: The aim of this study is to clarify the efficacy of transcutaneous periodic vibrational stimulation(TPVS）on gait and balance function in patients with spinocerebellar degeneration…Co-occurrence of Spinal Muscular Atrophy Type 2 and Huntington’s Disease
Objective: To describe a unique case of co-occurring SMA2 and HD in a patient. Background: Huntington’s Disease (HD) is an autosomal dominant neurodegenerative disorder caused…Novel findings in a Swedish RFC1-related disorder cohort
Objective: This study aims to clinically characterize a Swedish cohort of patients featuring RFC1 CANVAS/spectrum disorders. Background: Biallelic pentanucleotide expansions in the RFC1 gene are…Huntington disease in a Patient with Extensive Psychiatric History
Objective: Huntington's Disease (HD) is an autosomal dominant neurodegenerative disorder resulting from an expansion of CAG trinucleotide repeats in the gene encoding the huntingtin protein.…
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