Late-Onset Huntington’s Disease Misdiagnosed as Post-Stroke Chorea: A Case Report
Objective: Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder caused by CAG repeat expansion in the HTT gene, typically presenting in midlife with chorea,…Cryptococcal Meningitis Presenting with Lower Body Parkinsonism and Generalized Chorea: A Case Report
Objective: To report a case of cryptococcal meningitis in a person living with Human immunodeficiency virus (HIV) presented with lower body parkinsonism and subsequent generalized…Early Reduction in Cerebral Histamine 3 Receptor Expression in People with Huntington’s Disease: Results from the iMarkHD Study
Objective: To quantify histamine 3 receptor (H3R) expression using positron emission tomography (PET) in people with Huntington’s disease (PwHD) across different stages of disease progression.…Extracellular Small RNAs in Huntington’s disease: from Brain to CSF Analysis
Objective: To investigate a panel of extracellular small non-coding RNAs (sRNAs) in Huntington's disease gene expansion individuals (HDGE) and its potential as CSF biomarkers. Background:…Machine Learning-Driven Analysis of Epigenetic Signatures in Juvenile Huntington’s Disease: Investigating Histone Modification Dynamics
Objective: To investigate the role of histone modifications in Juvenile Huntington’s Disease (JHD) using machine learning, aiming to identify novel epigenetic biomarkers predictive of disease…Strategies for Participant Retainment in Large Observational Studies in Movement Disorders: a Single Centre Experience
Objective: To explore common reasons for participant attrition and recruitment barriers in observational studies in people affected by movement disorders.To explore common reasons for participant…A Case report of Progressive Supranuclear Palsy with Cerebellar Ataxia and Chorea
Objective: To report a case of progressive supranuclear palsy cerebellar type (PSP-C) with choreiform movements. Background: PSP-C is a rare subtype of PSP characterized by…Reversible Uremic Striatopathy Presenting as Acute Generalized Myoclonus and Chorea in a Patient with End Stage Renal Disease: A video-case report
Objective: To highlight uremic striatopathy as a reversible metabolic cause of acute hyperkinetic movement disorder in patients with end stage renal disease. Background: Uremic striatopathy…Incidence and movement disorders associated with Steroid-Responsive Encephalopathy Associated with Autoimmune Thyroiditis (SREAT) in the Princess Maha Chakri Sirindhorn Medical Center (MSMC)
Objective: To identify incidence and clinical features of SREAT patients in MSMC. Background: SREAT patients could present with encephalopathy with various neurological abnormalities, including behavioral…Suicidal Ideation and the Hippocampal Histaminergic System in Huntington’s Disease: A PET Study
Objective: To determine whether presence and severity of suicidal ideation (SI) are associated with hippocampal volume and histamine H3 receptor (H3R) PET uptake in people with Huntington’s disease (PwHD). Background: Suicidal ideation occurs in approximately 8–27% of PwHD, yet its causes remain unclear(1–3). The…
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