Register
Community
Overview
Experts
Editors
Fellows
Code of conduct
AI Guidelines for Physicians
Company
About Us
FAQs
Privacy Policy
Terms of Use
Careers
Programs
News
News Releases
Press Coverage
Publications
Blog
Contact Us
Sign in
Please select the option that best describes you:
Topics:
Neurology
•
Child Neurology
How does choice of enzyme replacement therapy and monitoring parameters for late-onset Pompe disease differ from infantile onset disease?
Related Questions
How do you decide when to pursue genetic testing for cerebral palsy?
What is your approach to a child with toe walking with a reassuring exam but a family history of difficulty walking?
What is your approach to a pediatric patient presenting with a new daily persistent headache?
When, if ever, would you pursue genetic testing in an asymptomatic child with multiple first-degree relatives with epilepsy?
When do you consider surgery for patients with Sturge Weber?
When, if ever, do you use therapeutic hypothermia (targeted temperature management) in a non-neotal pediatric cardiac arrest patient?
When do you consider testing with stroke gene panels in young stroke patients?
What behavioral interventions have you found most effective for managing self-injurious behavior in autism?
What criteria do you use to diagnose ataxic cerebral palsy?
What workup do you consider for a developmentally typical child with multiple large café au lait macules but no other signs of neurofibromatosis?