Recrudescence of a Compensated Hemidystonia-hemiatrophy Syndrome After COVID-19 Infection
Objective: To educate readers about a unique presentation of hemidystonia-hemiatrophy syndrome which presented after an infection with COVID-19 Background: Hemidystonia-hemiatrophy syndrome is a rare disorder…Exploring the non-invasive epigenetic screening test for hereditary dystonia DYT-KMT2B
Objective: To explore the altered H3K4me3 levels in non-neural tissue of DYT-KMT2B patients. Background: DYT-KMT2B, also known as DYT28, is a childhood-onset hereditary dystonia caused…Increased cerebellar grey matter in writer’s cramp patients: a morphometric signature of symptom compensation
Objective: This study focused on grey matter changes in the cerebellum by performing voxel-based morphometry (VBM) on infratentorial MRI scans of writers' cramp (WC) patients,…Visual Temporal Discrimination Threshold using a Virtual Reality Paradigm in Cervical Dystonia
Objective: To develop a Virtual Reality (VR) application to test temporal discrimination thresholds in cervical dystonia patients within an outpatient environment. Background: Temporal discrimination threshold…A Survey of Immunological Mechanisms in Cervical Dystonia
Objective: The overall goal was to delineate which aspects of the immune system may be most relevant to the biology of CD. Background: Although several…Movement Disorders Associated with Infectious Encephalitis in Pediatric Patients
Objective: The objective of our study is to report the clinical and imaging profile of a cohort of pediatric patients with movement disorders (MDs) associated…DPPX Autoimmune Encephalitis Associated with Severe Multifocal Dystonia.
Objective: To describe a novel motor phenomenology in an individual diagnosed with anti-DPPX encephalitis at our institution and to compare it with previously known phenotypic…Clinico-radiological Spectrum and Predictors of Disease Severity in Neurological Wilson Disease: A Single Center Observational Study.
Objective: To determine the Clinical and radiological spectrum of neurological Wilson’s disease (WD) and predictors of disease severity. Background: Wilson’s Disease (WD) is autosomal recessive,…Antibody-mediated movement disorders: a single-centre retrospective study
Objective: This study aims to evaluate the clinical spectrum of antibody-associated movement disorders from a single centre. Background: There is an increasing recognition of movement…Severe movement disorder initially suspected of being conversion – key insights from the psychiatrist
Objective: The review of a case diagnosed as Conversion Disorder (CD) in a University Movement Disorders clinic is presented here. As this patient eventually recovered…
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