K. Verhaert

Critical evaluation of four different seizure detection systems tested on one patient with focal and generalized tonic and clonic seizures

A. V. D. Vel, B. Ceulemans, K. Verhaert, 2014, Epilepsy & Behavior.

Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations

I. Scheffer, L. Lagae, S. Berkovic, 2010, Neurology.

Gorlin-Goltz syndrome in a child: case report and clinical review.

P. Parizel, F. Vanhoenacker, K. Verhaert, 2008, JBR-BTR : organe de la Societe royale belge de radiologie (SRBR) = orgaan van de Koninklijke Belgische Vereniging voor Radiologie.

Early‐onset absence epilepsy caused by mutations in the glucose transporter GLUT1

I. Scheffer, S. Berkovic, H. Lerche, 2009, Annals of neurology.

Cognitive outcomes following epilepsy in infancy: A longitudinal community‐based study

R. Scott, M. de Haan, J. Helen Cross, 2018, Epilepsia.

12 Acute Symptomatic Epileptic Seizures

R. Scott, K. Verhaert, 2010 .