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

Epilepsia (Copenhagen), 2012-07, Vol.53 (7), p.1131-1139

2012

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Developmental unilateral facial palsy in a newborn: six cases and literature review

European journal of pediatrics, 2020-03, Vol.179 (3), p.367-375

2020

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Treatment of Focal-Onset Seizures in Children: Should This Be More Etiology-Driven?

Frontiers in neurology, 2022-03, Vol.13, p.842276-842276

2022

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KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy

Annals of neurology, 2012-01, Vol.71 (1), p.15-25

2012

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

American journal of human genetics, 2018-12, Vol.103 (6), p.1022-1029

2018

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Low-dose fenfluramine in the treatment of neurologic disorders: experience in Dravet syndrome

Therapeutic Advances in Neurological Disorders, 2015-11, Vol.8 (6), p.328-338

2015

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Pharmacological characterization of an antisense knockdown zebrafish model of Dravet syndrome: inhibition of epileptic seizures by the serotonin agonist fenfluramine

PloS one, 2015-05, Vol.10 (5), p.e0125898-e0125898

2015

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

Epilepsia (Copenhagen), 2020-06, Vol.61 (6), p.1142-1155

2020

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

Annals of neurology, 2009-09, Vol.66 (3), p.415-419

2009

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De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy

American journal of human genetics, 2001-06, Vol.68 (6), p.1327-1332

2001

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Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy

Pediatric neurology, 2004-04, Vol.30 (4), p.236-243

2004

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A randomized double-blind, placebo-controlled trial of ganaxolone in children and adolescents with fragile X syndrome

Journal of neurodevelopmental disorders, 2017-08, Vol.9 (1), p.26-26, Article 26

2017

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Childhood chronic inflammatory demyelinating polyneuroradiculopathy – Three cases and a review of the literature

European journal of paediatric neurology, 2012-07, Vol.16 (4), p.315-331

2012

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Recurrent NEDD4L Variant in Periventricular Nodular Heterotopia, Polymicrogyria and Syndactyly

Frontiers in genetics, 2020-02, Vol.11, p.26

2020

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Clinical Investigation of French Maritime Pine Bark Extract on Attention-Deficit Hyperactivity Disorder as compared to Methylphenidate and Placebo: Part 1: Efficacy in a Randomised Trial

Journal of functional foods, 2022-10, Vol.97, p.105246, Article 105246

2022

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Overall management of patients with Dravet syndrome

Developmental medicine and child neurology, 2011-04, Vol.53 (s2), p.19-23

CEULEMANS, BERTEN

2011

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Pseudomonas aeruginosa in children with cerebral palsy: a prospective study

Frontiers in pediatrics, 2023, Vol.11, p.1267345-1267345

2023

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Clinical Investigation of French Maritime Pine Bark Extract on Attention-Deficit Hyperactivity Disorder as compared to Methylphenidate and Placebo: Part 2: Oxidative Stress and Immunological Modulation

Journal of functional foods, 2022-10, Vol.97, p.105247, Article 105247

2022

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SCN1B‐linked early infantile developmental and epileptic encephalopathy

Annals of clinical and translational neurology, 2019-12, Vol.6 (12), p.2354-2367

2019

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Are GMI gangliosidosis and Morquio type B two different disorders or part of one phenotypic spectrum?

JIMD reports, 2021-05, Vol.59 (1), p.90-103

2021

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Effect of Pycnogenol® on attention-deficit hyperactivity disorder (ADHD): study protocol for a randomised controlled trial

Trials, 2017-03, Vol.18 (1), p.145-9, Article 145

2017

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Treatment and long term outcome in West syndrome: The clinical reality. A multicentre follow up study

Seizure (London, England), 2010-04, Vol.19 (3), p.159-164

2010

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Early myoclonic encephalopathy caused by a disruption of the neuregulin-1 receptor ErbB4

European journal of human genetics : EJHG, 2009-03, Vol.17 (3), p.378-382

2009

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

Developmental unilateral facial palsy in a newborn: six cases and literature review

Treatment of Focal-Onset Seizures in Children: Should This Be More Etiology-Driven?

KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy

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

Low-dose fenfluramine in the treatment of neurologic disorders: experience in Dravet syndrome

Pharmacological characterization of an antisense knockdown zebrafish model of Dravet syndrome: inhibition of epileptic seizures by the serotonin agonist fenfluramine

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

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

Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders

De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy

Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy

A randomized double-blind, placebo-controlled trial of ganaxolone in children and adolescents with fragile X syndrome

Childhood chronic inflammatory demyelinating polyneuroradiculopathy – Three cases and a review of the literature

Recurrent NEDD4L Variant in Periventricular Nodular Heterotopia, Polymicrogyria and Syndactyly

Clinical Investigation of French Maritime Pine Bark Extract on Attention-Deficit Hyperactivity Disorder as compared to Methylphenidate and Placebo: Part 1: Efficacy in a Randomised Trial

Overall management of patients with Dravet syndrome

Pseudomonas aeruginosa in children with cerebral palsy: a prospective study

Clinical Investigation of French Maritime Pine Bark Extract on Attention-Deficit Hyperactivity Disorder as compared to Methylphenidate and Placebo: Part 2: Oxidative Stress and Immunological Modulation

SCN1B‐linked early infantile developmental and epileptic encephalopathy

REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31

Are GMI gangliosidosis and Morquio type B two different disorders or part of one phenotypic spectrum?

Effect of Pycnogenol® on attention-deficit hyperactivity disorder (ADHD): study protocol for a randomised controlled trial

Treatment and long term outcome in West syndrome: The clinical reality. A multicentre follow up study

Early myoclonic encephalopathy caused by a disruption of the neuregulin-1 receptor ErbB4

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