Feasibility of Remote Identification of Catatonia Across Different Motor Presentations
Objective: To evaluate the feasibility of the identification of catatonia by trained raters through remote viewing of motor assessments across patients with differing motor profiles…Intensive Neurophysiological Rehabilitation System As a New Approach for Treatment of ASD Children
Objective: Rehabilitation of ASD children is the issue of the day as it's attributed to constantly increasing quantity of autistic children. Background: Existing rehabilitation approaches…Feasibility of Reliable, Remote Assessment of a 13-year-old Boy Who Stopped Talking
Objective: To assess the feasibility of reliable, remote assessments of videos of a 13-year-old boy who stopped talking Background: The sudden absence of speech in…Screening of autistic traits in people with functional neurological disorders
Objective: To examine self-reported autistic traits in people with functional neurological disorders (FND) and the prevalence of diagnosed autism spectrum disorders (ASD) among people with…The severity of tics in patients with Gilles de la Tourette syndrome and comorbid Autism Spectrum Disorder
Objective: The aim of this study was to compare characteristics and severity of tics in patients with Gilles de la Tourette Syndrome (GTS) and comorbid…Catatonic Syndrome in Covid-19 Infection: Medication Treatment or Hyperbaric Oxygen Therapy.
Objective: Catatonic syndrome, or catatonia (from other Greek κατατείνω - “stretch, strain”), is a psychopathological syndrome (a group of symptoms), the main clinical manifestation of…Impairment of Neurological Ontogenesis in Children with Austism Spectrum Disorders
Objective: To assess level of involvement of neurological impairment in children with Autism Spectrum Disorders (ASD). Background: Autism Spectrum Disorders are not singly related to…Development of the UK hereditary spastic paraplegia registry: Analysis of SPAST patients reveals high rate of psychiatric comorbidities
Objective: To (1) describe the genetic variability, phenotype and epidemiology of spastin mutation in HSP patients (2) create the UK HSP register with a focus…A rapid chemical-genetic screen utilising impaired movement phenotypes in caenorhabditis elegans
Objective: Development of a fast and unbiased screening method to identify C. elegans mutants with movement disabilities and drugs to improve impaired locomotion. Background: Identifying…
Abstracts from the International Congress of Parkinson’s and Movement Disorders.