Knowledge and attitude towards movement disorders among final year medical students in a Nigerian university
Objective: The study was aimed to evaluate knowledge and attitude of medical students towards movement disorders. Background: The understanding of movement disorders could pose a…Public awareness and education of Parkinson’s Disease among Nepalese Population
Objective: This study aimed to evaluate the knowledge of Parkinson’s Disease(PD) among general population and educate them with the clinical features of this disease for…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…
Abstracts from the International Congress of Parkinson’s and Movement Disorders.