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…Phenytoin Intoxication Masquerading as Generalized Chorea: A Case of Iatrogenic Double-Prescribing
Objective: To report a rare case of phenytoin-induced generalized chorea resulting from inadvertent medication duplication across multiple healthcare facilities, highlighting a preventable cause of acute…Intrinsic Suppression of the NRF2–Ferroptosis Defense Axis Defines Selective Vulnerability of D2-Striosome Neurons in Huntington’s Disease
Objective: This study mapped baseline stress-response and cell death programs in healthy human striatal populations to identify intrinsic molecular constraints in D2-striosome neurons and their…Late onset chorea secondary to antiphospholipid syndrome with radiological correlation on brain FDG-PET: a case report.
Objective: To describe chorea as the initial manifestation of antiphospholipid syndrome (APS) and its radiological correlation on brain FDG-PET as an autoimmune movement disorder. Background:…“Unexplained” Chorea Explained by Neuronal Antibodies: A Dutch Cohort Study
Objective: To identify neuronal antibodies in patients with unexplained chorea. Background: In recent years, autoimmune causes of chorea are increasingly recognized and the number of…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:…
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