Abstract Details

Title Familial Episodic Encephalopathy, Dysarthria, and Paralysis Is Associated with a Dominantly Inherited Mutation in ATP1A3

Topic Child Neurology and Developmental Neurology

Presentation(s) (-)

Poster/Presentation
Number 335

Background

Objective

Design/Methods

Results

Conclusions

Authors/Disclosures
Gyula Acsadi, MD, FAAN (Connecticut Children'S Medical Center/UConn) PRESENTER	Dr. Acsadi has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Biogen. Dr. Acsadi has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Avexis. Dr. Acsadi has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Serepta. Dr. Acsadi has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Genentech. Dr. Acsadi has received personal compensation in the range of $5,000-$9,999 for serving on a Speakers Bureau for Biogen.
Richard S. Young, MD, FAAN (Connecticut Childrens Specialty Group)	Dr. Young has nothing to disclose.
	No disclosure on file
	No disclosure on file
	No disclosure on file
	No disclosure on file
Kathryn J. Swoboda, MD	Dr. Swoboda has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Biogen. Dr. Swoboda has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Biogen. The institution of Dr. Swoboda has received research support from Biogen.
	No disclosure on file