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Human Molecular Genetics|October 26, 2005
Susceptibility genes for complex epilepsyJohn C Mulley, Ingrid E Scheffer, Louise A Harkin, et al.
Epilepsia|February 27, 2009
EEG features of absence seizures in idiopathic generalized epilepsy: impact of syndrome, age, and stateLynette Grant Sadleir, Ingrid E Scheffer, Sherry Smith, et al.
Epilepsy & Behavior : E&B|August 29, 2020
Cognitive, behavioral, and social functioning in children and adults with Dravet syndromeAmy Brown, Marta Arpone, Amy L Schneider, et al.
Epilepsia Open|July 4, 2024
Practical considerations for the use of fenfluramine to manage patients with Dravet syndrome or Lennox-Gastaut syndrome in clinical practiceElaine C Wirrell, Lieven Lagae, Ingrid E Scheffer, et al.
Epilepsia|March 21, 2002
Chromosomal abnormalities and epilepsy: a review for clinicians and gene huntersRita Singh, R J McKinlay Gardner, Kathryn M Crossland, et al.
Epilepsia|February 27, 2025
Operational definition of developmental and epileptic encephalopathies to underpin the design of therapeutic trialsIngrid E Scheffer, Jacqueline French, Kette D Valente, et al.
Neurology. Genetics|April 12, 2016
In silico prioritization based on coexpression can aid epileptic encephalopathy gene discoveryKaren L Oliver, Vesna Lukic, Saskia Freytag, et al.
Pharmacological Reviews|December 22, 2017
Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted TherapiesJulia Oyrer, Snezana Maljevic, Ingrid E Scheffer, et al.
Seminars in Neurology|May 17, 2013
Racemose neurocysticercosisRohit R Das, Kristyn J Tekulve, Atul Agarwal, et al.
Epilepsia|April 6, 2011
The genetics of Dravet syndromeCarla Marini, Ingrid E Scheffer, Rima Nabbout, et al.
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