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:
Epilepsy
•
Neurology
•
Child Neurology
•
Primary Care
When, if ever, would you pursue genetic testing in an asymptomatic child with multiple first-degree relatives with epilepsy?
Related Questions
How do you use aspirin in pre-symptomatic Sturge Weber patients?
How do you utilize at-home seizure monitoring devices for your patients with epilepsy?
Would you use bupropion for mood disorder or substance use in an adult patient with previous childhood seizures that resolved?
What is your approach to dosing phenobarbital for a neonate on intermittent hemodialysis?
Besides patient preference, what factors guide your decision to treat SeLECTs patients with antiseizure medications?
How do you approach anti-seizure medication management when it was started by another team for a seizure-naive patient before/after craniotomy for a tumor?
When would you start antiseizure medications in tuberous sclerosis before onset of seizures?
What workup do you consider for a developmentally typical child with multiple large café au lait macules but no other signs of neurofibromatosis?
How do you adjust the management of epilepsy in patients who are planning to fast?
How do you discontinue ketogenic diets previously used as a treatment for epilepsy?
