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Epilepsia|April 17, 2015
Early and effective treatment of KCNQ2 encephalopathyTiziana Pisano, Adam L Numis, Sinéad B Heavin, et al.
Vaccine|September 13, 2018
Transcriptome profiling in blood before and after hepatitis B vaccination shows significant differences in gene expression between responders and non-respondersEsther Bartholomeus, Nicolas De Neuter, Pieter Meysman, et al.
Vaccine|March 14, 2020
Transcriptomic profiling of different responder types in adults after a Priorix® vaccinationEsther Bartholomeus, Nicolas De Neuter, Arvid Suls, et al.
Genes and Immunity|June 16, 2018
Memory CD4+ T cell receptor repertoire data mining as a tool for identifying cytomegalovirus serostatusNicolas De Neuter, Esther Bartholomeus, George Elias, et al.
Epilepsy Research|January 12, 2013
The role of SLC2A1 in early onset and childhood absence epilepsiesHiltrud Muhle, Ingo Helbig, Tobias Guldberg Frøslev, et al.
Epilepsy Research|June 20, 2015
Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?Felicitas Becker, Julian Schubert, Sarah Weckhuysen, et al.
Annals of Neurology|December 10, 2013
Dominant-negative effects of KCNQ2 mutations are associated with epileptic encephalopathyGökce Orhan, Merle Bock, Dorien Schepers, et al.
The Journal of Infectious Diseases|August 23, 2025
Genetic landscape of a cohort of children with varicella-zoster virus encephalitis, cerebellitis and strokeFranziska Winzig, Kerstin De Keukeleere, Esther Bartholomeus, et al.
Annals of Neurology|October 3, 2009
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1Arvid Suls, Saul A Mullen, Yvonne G Weber, et al.
EMBO Molecular Medicine|November 29, 2015
Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathyBorislav Dejanovic, Tania Djémié, Nora Grünewald, et al.
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