COURSE PURPOSE
Journal CME highlights various articles covering relevant issues, developments and research topics in the area of movement disorders. Articles are selected from Movement Disorders, the official Journal of the International Parkinson and Movement Disorder Society.
LEARNING OBJECTIVES
Upon completion of this activity, learners will be able to:
1. Understand the need to better characterize the clinical phenotypes and genetic features of hereditary spastic paraplegia (HSP).
2. Assess the application of a combination of WES with MLPA to explore the genotype–phenotype correlations as well as the landscape and hallmarks of this study’s cohort.
3. Evaluate the proposed diagnostic flowchart to be used for sequentially detecting the causative genes in practice.
INTENDED AUDIENCE
This activity is intended for clinicians, other health professionals, researchers, policy makers from throughout the world, both MDS members and non-members, who interact with patients living with Movement Disorders.
HARDWARE AND SOFTWARE REQUIREMENTS
1. Active Internet connection (DSL or Cable). Dial-up connection will have constant buffering problem.
2. Compatible with Windows PC and MAC (256 MB of RAM or higher).
3. Activity is best viewed on Internet Explorer 9.0 or higher, Safari 5.0 or higher and Firefox 29.0 or higher.
4. Adobe Flash Player 12.0 (or higher).
5. Adobe Reader to print certificate.