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List of works by Berten Ceulemans

Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies

scientific article published on 01 December 2018

Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

scientific article published on 01 August 2019

Diagnostic implications of genetic copy number variation in epilepsy plus

scientific article published on 13 March 2019

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

scientific article published in September 2009

Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients

scientific article

Extremely elevated cerebrospinal fluid protein levels in a child with neurologic symptoms: beware of haemophagocytic lymphohistiocytosis.

scientific article

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.

scientific article published on 4 March 2017

IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

scientific article published on 12 September 2018

Lessons learned from 40 novel PIGA patients and a review of the literature

scientific article published on 26 May 2020

Long-term home monitoring of hypermotor seizures by patient-worn accelerometers ⬇️

scientific article published on December 6, 2012

PRRT2 mutations: exploring the phenotypical boundaries.

scientific article published on 7 October 2013

STXBP1 promotes Weibel-Palade body exocytosis through its interaction with the Rab27A effector Slp4-a

scientific article published on 3 April 2014

Successful use of fenfluramine as an add-on treatment for Dravet syndrome ⬇️

scientific article published on May 3, 2012

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