RecruitingNCT00041600
Human Epilepsy Genetics--Neuronal Migration Disorders Study
Sponsor
Harvard University Faculty of Medicine
Enrollment
3,500 participants
Start Date
Apr 1, 1996
Study Type
OBSERVATIONAL
Conditions
Summary
The purpose of this study is to identify genes responsible for epilepsy, brain malformations and disorders of human cognition.
Eligibility
Inclusion Criteria2
- Males and females of any age.
- Persons with a brain malformation or disorder of cognition (familial intellectual disability \[previously known as mental retardation\] or autism).
Exclusion Criteria1
- Persons without a brain malformation or disorder of cognition (familial intellectual disability (previously known as mental retardation\] or autism).
Interested in this trial?
Get notified about updates and connect with the research team.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT00041600
Related Trials
Tumor Related Epilepsy
NCT026393251 location
Investigation of Blood-Brain-Barrier Breakdown Using Manganese Magnetic Resonance Imaging in Drug-Resistant Epilepsy
NCT025318801 location
AI-Based Mobile Intervention on Medication Non-Adherence and Transition
NCT074450742 locations
MEHMO Natural History and Biomarkers
NCT060191821 location
Transgenerational Metabolic-Immune Biomarkers of Neurological and Neurodevelopmental Disorders
NCT043227342 locations