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Berten Ceulemans

Showing results (81-90 of 137) with videos related to

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Annals of Clinical and Translational Neurology|November 12, 2019
SCN1B-linked early infantile developmental and epileptic encephalopathyAlec Aeby, Claudine Sculier, Alexandra A Bouza, et al.
Journal of Neurodevelopmental Disorders|August 3, 2017
A randomized double-blind, placebo-controlled trial of ganaxolone in children and adolescents with fragile X syndromeAndrew Ligsay, Anke Van Dijck, Danh V Nguyen, et al.
Seizure|November 12, 2021
Impact of fenfluramine on the expected SUDEP mortality rates in patients with Dravet syndromeJ Helen Cross, Bradley S Galer, Antonio Gil-Nagel, et al.
Seizure|October 18, 2011
Development of an electronic decision tool to support appropriate treatment choice in adult patients with epilepsy--Epi-Scope(®)Benjamin Legros, Paul Boon, Berten Ceulemans, 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.
European Journal of Human Genetics : EJHG|September 11, 2014
Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndromeGea Beunders, Sonja A de Munnik, Nathalie Van der Aa, 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.
Archives of Neurology|February 8, 2012
Novel infantile-onset leukoencephalopathy with high lactate level and slow improvementMarjan E Steenweg, Adeline Vanderver, Berten Ceulemans, et al.
Blood|April 5, 2014
STXBP1 promotes Weibel-Palade body exocytosis through its interaction with the Rab27A effector Slp4-aDorothee van Breevoort, Ambrosius P Snijders, Nicola Hellen, et al.
Pageof 14

Showing results (81-90 of 137) with videos related to

Sort By:
Pageof 14
Annals of Clinical and Translational Neurology|November 12, 2019
SCN1B-linked early infantile developmental and epileptic encephalopathyAlec Aeby, Claudine Sculier, Alexandra A Bouza, et al.
Journal of Neurodevelopmental Disorders|August 3, 2017
A randomized double-blind, placebo-controlled trial of ganaxolone in children and adolescents with fragile X syndromeAndrew Ligsay, Anke Van Dijck, Danh V Nguyen, et al.
Seizure|November 12, 2021
Impact of fenfluramine on the expected SUDEP mortality rates in patients with Dravet syndromeJ Helen Cross, Bradley S Galer, Antonio Gil-Nagel, et al.
Seizure|October 18, 2011
Development of an electronic decision tool to support appropriate treatment choice in adult patients with epilepsy--Epi-Scope(®)Benjamin Legros, Paul Boon, Berten Ceulemans, 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.
European Journal of Human Genetics : EJHG|September 11, 2014
Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndromeGea Beunders, Sonja A de Munnik, Nathalie Van der Aa, 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.
Archives of Neurology|February 8, 2012
Novel infantile-onset leukoencephalopathy with high lactate level and slow improvementMarjan E Steenweg, Adeline Vanderver, Berten Ceulemans, et al.
Blood|April 5, 2014
STXBP1 promotes Weibel-Palade body exocytosis through its interaction with the Rab27A effector Slp4-aDorothee van Breevoort, Ambrosius P Snijders, Nicola Hellen, et al.
Pageof 14