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European Journal of Obstetrics, Gynecology, and Reproductive Biology|April 28, 2026
Rewriting the history of Paget's disease: From Arderne's medieval case to Crocker's first extramammary description (1370-1889)Wiebren A Tjalma, Jan Bosteels, Filip Thiessen, et al.
Epilepsy & Behavior : E&B|July 26, 2016
Automated non-EEG based seizure detection: Do users have a say?Anouk Van de Vel, Katrien Smets, Kristien Wouters, et al.
Acta Neurologica Belgica|June 25, 2015
The spectrum of epilepsy caused by POLG mutationsWouter Janssen, Annelies Quaegebeur, Gert Van Goethem, et al.
Neuroradiology|September 10, 2005
Meningoencephalitis caused by Streptococcus pneumoniae: a diagnostic and therapeutic challenge. Diagnosis with diffusion-weighted MRI leading to treatment with corticosteroidsPhilippe G Jorens, Paul M Parizel, Hendrik E Demey, et al.
Human Mutation|July 9, 2009
The SCN1A variant database: a novel research and diagnostic toolLieve R F Claes, Liesbet Deprez, Arvid Suls, et al.
Acta Neurologica Belgica|May 1, 2012
Recommendations for the treatment of epilepsy in adult patients in general practice in Belgium: an updatePaul Boon, Sebastiaan Engelborghs, Henri Hauman, et al.
Orphanet Journal of Rare Diseases|February 15, 2017
STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutationsStefanie Nicole Hayer, Tine Deconinck, Benjamin Bender, et al.
Acta Neurologica Belgica|September 11, 2013
First line management of prolonged convulsive seizures in children and adults: good practice pointsLiesbeth De Waele, Paul Boon, Berten Ceulemans, et al.
BMC Medical Genetics|July 21, 2015
First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsyKatrien Smets, Anna Duarri, Tine Deconinck, et al.
Human Mutation|May 20, 2003
De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancyLieve Claes, Berten Ceulemans, Dominique Audenaert, et al.
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