Glucose transporter type I deficiency syndrome: Epilepsy phenotypes and outcomes
Pong, Amanda W., Geary, Brianna R., Engelstad, Kris M., Natarajan, Ashwini, Yang, Hong, De Vivo, Darryl C.
Published in Epilepsia (Copenhagen) (01.09.2012)
Published in Epilepsia (Copenhagen) (01.09.2012)
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Journal Article
Impact of regulatory safety warnings and restrictions on drug treatment of epilepsy
Pong, Amanda W, Tyrlikova, Ivana, Giermek, Alexander J, Klein, Pavel
Published in Expert opinion on drug safety (01.02.2023)
Published in Expert opinion on drug safety (01.02.2023)
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Journal Article
Epilepsy: expert opinion on emerging drugs in phase 2/3 clinical trials
Pong, Amanda W, Ross, Jonathan, Tyrlikova, Ivana, Giermek, Alexander J, Kohli, Maya P, Khan, Yousef A, Salgado, Roger D, Klein, Pavel
Published in Expert opinion on emerging drugs (02.01.2022)
Published in Expert opinion on emerging drugs (02.01.2022)
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Journal Article
A novel mutation in the aristaless domain of the ARX gene leads to Ohtahara syndrome, global developmental delay, and ambiguous genitalia in males and neuropsychiatric disorders in females
Ekşioğlu, Yaman Z., Pong, Amanda W., Takeoka, Masanori
Published in Epilepsia (Copenhagen) (01.05.2011)
Published in Epilepsia (Copenhagen) (01.05.2011)
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Journal Article
High‐dose intravenous levetiracetam for acute seizure exacerbation in children with intractable epilepsy
Depositario‐Cabacar, Dewi T., Peters, Jurriaan M., Pong, Amanda W., Roth, Julie, Rotenberg, Alexander, Riviello, James J., Takeoka, Masanori
Published in Epilepsia (Copenhagen) (01.07.2010)
Published in Epilepsia (Copenhagen) (01.07.2010)
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Journal Article
A novel mutation in the aristaless domain of the ARX gene leads to Ohtahara syndrome, global developmental delay, and ambiguous genitalia in males and neuropsychiatric disorders in females: ARX, Ohtahara Syndrome, Psychomotor Delay
Ekşioğlu, Yaman Z., Pong, Amanda W., Takeoka, Masanori
Published in Epilepsia (Copenhagen) (01.05.2011)
Published in Epilepsia (Copenhagen) (01.05.2011)
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Journal Article