Acceptability and Effectiveness of an Online Curriculum in Movement Disorders for Neurology Housestaff: A pilot study
Objective: To determine the acceptability, feasibility, and effect on knowledge of an online curriculum in movement disorders for neurology housestaff. Background: Neurology residents often get…The development of a patient education and treatment programme for people with Parkinson’s disease
Objective: To ensure we have a flexible education and treatment programme format, designed for people with Parkinson's disease (PWP), relevant to their time since diagnosis,…Neurology Residents Versus a Mobile Medical Application in deducing differential diagnoses in Movement Disorders: A multi-center, cross-sectional, observational study
Objective: To test the hypothesis that the differentials generated by the Mobile Medical Application are more clinically relevant and complete to the ones derived by…Adaptor Protein Complex 4-associated Hereditary Spastic Paraplegia (AP-4-HSP): A Paradigm of Childhood-Onset Hereditary Spastic Paraplegia Caused By Defective Protein Trafficking
Objective: Aims of this study include: 1) to generate induced pluripotent stem cell (iPSC)-derived neurons from patients with AP-4-associated HSP; 2) to characterize these neurons…Pantothenate kinase-associated neurodegeneration in Tunisian families
Objective: To describe clinical features, imaging and genetic findings of 6 Tunisian families diagnosed with PKAN. Background: Pantothenate kinase-associated neurodegeneration (PKAN) is an autosomal recessive…Assessment, identification and classification of movement disorders in 22q11.2 deletion syndrome
Objective: To assess the nature and frequency of movement disorders in children with molecularly confirmed 22q11.2 Deletion Syndrome. Background: 22q11.2 Deletion Syndrome (22q11.2DS) is a…Pre-status and status dystonicus in children and adolescents
Objective: Retrospective analysis of an 8-years' experience in diagnosis, management and follow-up of children experiencing Status dystonicus (SD) and pre-SD. Background: SD is considered the most…TUBB4A mutation: Expansion of H-ABC phenotype with apparent iron accumulation in the basal ganglia – case report and literature review
Objective: This case report expand the phenotype of hypomyelination with atrophy of the basal ganglia and cerebellum. Background: Background: Hypomyelination with atrophy of the basal ganglia…Optimal treatment of geniospasm: a case report and review of the literature
Objective: To present a case of geniospasm in a child successfully treated with botulinum toxin injections and to review previously reported cases in the literature…Management of life threatening dyskinesias in GNAO1 related movement disorder: two new cases and review of the literature
Objective: To present two cases of GNAO1 related movement disorder associated with life threatening persistent chorea successfully managed with bilateral GPi deep brain stimulation (GPi-DBS)…
Abstracts from the International Congress of Parkinson’s and Movement Disorders.