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Berten Ceulemans

Showing results (61-70 of 137) with videos related to

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European Child & Adolescent Psychiatry|October 24, 2018
Oxidative stress and immune aberrancies in attention-deficit/hyperactivity disorder (ADHD): a case-control comparisonAnnelies A J Verlaet, Annelies Breynaert, Berten Ceulemans, et al.
Trials|March 30, 2017
Effect of Pycnogenol® on attention-deficit hyperactivity disorder (ADHD): study protocol for a randomised controlled trialAnnelies A J Verlaet, Berten Ceulemans, Helene Verhelst, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 4, 2019
Gait deviations in patients with dravet syndrome: A systematic reviewLore Wyers, Patricia Van de Walle, Aurélie Hoornweg, et al.
Seizure|February 13, 2010
Treatment and long term outcome in West syndrome: the clinical reality. A multicentre follow up studyLieven Lagae, Helène Verhelst, Berten Ceulemans, et al.
Plos One|May 13, 2015
Pharmacological characterization of an antisense knockdown zebrafish model of Dravet syndrome: inhibition of epileptic seizures by the serotonin agonist fenfluramineYifan Zhang, Angéla Kecskés, Daniëlle Copmans, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 20, 2014
Association of CDH11 with non-syndromic ASDAn Crepel, Veerle De Wolf, Nathalie Brison, et al.
Human Mutation|December 26, 2003
Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA)Liesbeth Rooms, Edwin Reyniers, Rob van Luijk, et al.
Seizure|August 28, 2016
Non-EEG seizure detection systems and potential SUDEP prevention: State of the art: Review and updateAnouk Van de Vel, Kris Cuppens, Bert Bonroy, et al.
Neuromuscular Disorders : NMD|March 26, 2011
Idebenone as a novel, therapeutic approach for Duchenne muscular dystrophy: results from a 12 month, double-blind, randomized placebo-controlled trialGunnar M Buyse, Nathalie Goemans, Marleen van den Hauwe, et al.
Human Molecular Genetics|October 19, 2020
Unravelling the disease mechanism for TSPYL1 deficiencyGunnar Buyse, Michela Di Michele, Anouck Wijgaerts, et al.
Pageof 14

Showing results (61-70 of 137) with videos related to

Sort By:
Pageof 14
European Child & Adolescent Psychiatry|October 24, 2018
Oxidative stress and immune aberrancies in attention-deficit/hyperactivity disorder (ADHD): a case-control comparisonAnnelies A J Verlaet, Annelies Breynaert, Berten Ceulemans, et al.
Trials|March 30, 2017
Effect of Pycnogenol® on attention-deficit hyperactivity disorder (ADHD): study protocol for a randomised controlled trialAnnelies A J Verlaet, Berten Ceulemans, Helene Verhelst, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 4, 2019
Gait deviations in patients with dravet syndrome: A systematic reviewLore Wyers, Patricia Van de Walle, Aurélie Hoornweg, et al.
Seizure|February 13, 2010
Treatment and long term outcome in West syndrome: the clinical reality. A multicentre follow up studyLieven Lagae, Helène Verhelst, Berten Ceulemans, et al.
Plos One|May 13, 2015
Pharmacological characterization of an antisense knockdown zebrafish model of Dravet syndrome: inhibition of epileptic seizures by the serotonin agonist fenfluramineYifan Zhang, Angéla Kecskés, Daniëlle Copmans, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 20, 2014
Association of CDH11 with non-syndromic ASDAn Crepel, Veerle De Wolf, Nathalie Brison, et al.
Human Mutation|December 26, 2003
Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA)Liesbeth Rooms, Edwin Reyniers, Rob van Luijk, et al.
Seizure|August 28, 2016
Non-EEG seizure detection systems and potential SUDEP prevention: State of the art: Review and updateAnouk Van de Vel, Kris Cuppens, Bert Bonroy, et al.
Neuromuscular Disorders : NMD|March 26, 2011
Idebenone as a novel, therapeutic approach for Duchenne muscular dystrophy: results from a 12 month, double-blind, randomized placebo-controlled trialGunnar M Buyse, Nathalie Goemans, Marleen van den Hauwe, et al.
Human Molecular Genetics|October 19, 2020
Unravelling the disease mechanism for TSPYL1 deficiencyGunnar Buyse, Michela Di Michele, Anouck Wijgaerts, et al.
Pageof 14