COMPARISON OF ELECTROPHYSIOLOGIC AND ULTRASOUND GUIDANCE FOR ONABOTULINUM TOXIN-A INJECTIONS IN FOCAL UPPER EXTREMITY SPASTICITY AND DYSTONIA
Objective: To investigate two targeting techniques for onabotulinum toxin-A (BoNT) injection for the treatment of focal hand dystonia and upper limb spasticity: guidance with electrical…Clinical heterogeneity of DYT-KMT2B mutation in a family with monozygotic twins
Objective: We describe the clinical heterogeneity of a Danish family with complex dystonia and a variant in KMT2B not previously reported. Background: Heterozygous mutations in…Dystonic Posturing with Athetoid Movements in Stroke Without Thalamic Lesion
Objective: Case study Background: Complex hyperkinetic movement disorders are a rare complication of stroke, frequently involving posterolateral contralateral thalamic lesions. One of the proposed mechanisms…A perception of knowledge on Parkinson’s disease among University students
Objective: The objective of this study is to understand the extent of awareness among the respondents on signs, symptoms, and management of Parkinson’s disease. Background:…Prevalence of Parkinsonism and Parkinson Disease in urban and rural populations in Latin America.
Objective: To estimate the prevalence and risk factors of parkinsonism and Parkinson Disease in elderly individuals from Latin America. Background: Parkinson’ s disease (PD) is…The prevalence and types of postural deformities in Thai patients with Parkinson’s disease: A single-center study
Objective: To address overall prevalence of Postural deformities(PostD) and each type of PostD (AC, TC, UC, and PS) in PD and healthy volunteers (HVs) Background:…Psychogenic movement disorders precipitated by post-lockdown return to school in adolescents: case series from Kenya
Objective: To describe three cases who presented with new-onset psychogenic movement disorders (PMD) after returning to school when the national lockdown was lifted. Background: PMD…Impaired saccadic inhibition in Huntington mutation carriers
Objective: To assess saccadic paradigms in asymptomatic Huntington disease mutation carriers. Background: Huntington’s disease (HD) is characterized by motor, cognitive and behavioural abnormalities, such as…Validation of smartphone-based active tests with structural neuroimaging in Huntington’s disease
Objective: Explore the association of smartphone-based active tests in the Roche Huntington’s disease (HD) Digital Monitoring Platform (dMP) with brain imaging. Background: Remote digital monitoring…Intergenerational repeat instability of TTTCA expansions in SAMD12 might be the major cause of the genetic anticipation in familial cortical myoclonic tremor with epilepsy
Objective: To delineate and analyze the relationship between genetic and clinical features in 78 patients from 23 familial cortical myoclonic tremor with epilepsy type 1 (FCMTE1) pedigrees. Background:…
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