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Vertigo and dizziness in children: When to consider a neurological cause

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2023-10, Vol.30 (7), p.505-509

2023

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Challenges and new perspectives of developmental cognitive EEG studies

NeuroImage (Orlando, Fla.), 2022-10, Vol.260, p.119508-119508, Article 119508

2022

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Fluoxetine as adjunctive therapy in pediatric patients with refractory epilepsy: A retrospective analysis

Epilepsy research, 2021-11, Vol.177, p.106780-106780, Article 106780

2021

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Familial KCNQ2 mutation: a psychiatric perspective

Psychiatric genetics, 2024-02, Vol.34 (1), p.24

2024

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Altered vaccine‐induced immunity in children with Dravet syndrome

Epilepsia (Copenhagen), 2018-04, Vol.59 (4), p.e45-e50

2018

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Stiripentol exhibits higher anticonvulsant properties in the immature than in the mature rat brain

Epilepsia (Copenhagen), 2013-12, Vol.54 (12), p.2082-2090

2013

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Seizures in Pediatric Patients With Primary Brain Tumors

Pediatric neurology, 2019-08, Vol.97, p.50-55

2019

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Serious Game with Electromyography Feedback and Physical Therapy in Young Children with Unilateral Spastic Cerebral Palsy and Equinus Gait: A Prospective Open-Label Study

Sensors (Basel, Switzerland), 2024-02, Vol.24 (5), p.1513

2024

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Loss of NDST1 N-sulfotransferase activity is associated with autosomal recessive intellectual disability

Human molecular genetics, 2024-02, Vol.33 (6), p.520-529

2024

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Perceptions of fever and fever management practices in parents of children with Dravet syndrome

Epilepsy & behavior, 2011-08, Vol.21 (4), p.446-448

2011

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Anti‐ictogenic and antiepileptogenic properties of perampanel in mature and immature rats

Epilepsia (Copenhagen), 2017-11, Vol.58 (11), p.1985-1992

2017

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Intellectual outcome from 1 to 5 years after epilepsy surgery in 81 children and adolescents: A longitudinal study

Seizure (London, England), 2021-10, Vol.91, p.384-392

2021

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Anti‐ictogenic and antiepileptogenic properties of brivaracetam in mature and immature rats

Epilepsia (Copenhagen), 2015-05, Vol.56 (5), p.800-805

2015

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Autosomal Dominant MPAN : Mosaicism Expands the Clinical Spectrum to Atypical Late‐Onset Phenotypes

Movement disorders, 2023-11, Vol.38 (11), p.2103-2115

2023

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Efficacy and tolerance of cannabidiol in the treatment of epilepsy in patients with Rett syndrome

Epilepsia open, 2024-02, Vol.9 (1), p.397-403

2024

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Slow Titration of Cannabidiol Add-On in Drug-Resistant Epilepsies Can Improve Safety With Maintained Efficacy in an Open-Label Study

Frontiers in neurology, 2020-08, Vol.11, p.829-829

2020

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Molecular and clinical descriptions of patients with GABAA receptor gene variants (GABRA1, GABRB2, GABRB3, GABRG2): A cohort study, review of literature, and genotype–phenotype correlation

Epilepsia (Copenhagen), 2022-10, Vol.63 (10), p.2519-2533

2022

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De novo mutations in CBL causing early-onset paediatric moyamoya angiopathy

Journal of medical genetics, 2017-08, Vol.54 (8), p.550

2017

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What is the optimal duration for vigabatrin monotherapy in patients with infantile spasms: 6 months or longer?

Seizure (London, England), 2021-10, Vol.91, p.503-506

2021

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Cognitive outcome in children with infantile spasms using a standardized treatment protocol. A five-year longitudinal study

Seizure (London, England), 2021-07, Vol.89, p.73-80

2021

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Pro-epileptogenic effects of viral-like inflammation in both mature and immature brains

Journal of neuroinflammation, 2016-12, Vol.13 (1), p.307, Article 307

2016

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Diagnosis delay in West syndrome: misdiagnosis and consequences

European journal of pediatrics, 2012-11, Vol.171 (11), p.1695-1701

2012

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Kingella kingae Sequence Type 25 Causing Endocarditis with Multiple and Severe Cerebral Complications

The Journal of pediatrics, 2016-02, Vol.169, p.326-326.e1

2016

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Impacts of an Interdisciplinary Developmental Follow-Up Program on Neurodevelopment in Congenital Heart Disease: The CINC Study

Frontiers in pediatrics, 2020-10, Vol.8, p.539451-539451

2020

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Vertigo and dizziness in children: When to consider a neurological cause

Challenges and new perspectives of developmental cognitive EEG studies

Fluoxetine as adjunctive therapy in pediatric patients with refractory epilepsy: A retrospective analysis

Familial KCNQ2 mutation: a psychiatric perspective

Altered vaccine‐induced immunity in children with Dravet syndrome

Stiripentol exhibits higher anticonvulsant properties in the immature than in the mature rat brain

Seizures in Pediatric Patients With Primary Brain Tumors

Serious Game with Electromyography Feedback and Physical Therapy in Young Children with Unilateral Spastic Cerebral Palsy and Equinus Gait: A Prospective Open-Label Study

Loss of NDST1 N-sulfotransferase activity is associated with autosomal recessive intellectual disability

Perceptions of fever and fever management practices in parents of children with Dravet syndrome

Anti‐ictogenic and antiepileptogenic properties of perampanel in mature and immature rats

Intellectual outcome from 1 to 5 years after epilepsy surgery in 81 children and adolescents: A longitudinal study

Anti‐ictogenic and antiepileptogenic properties of brivaracetam in mature and immature rats

Autosomal Dominant MPAN : Mosaicism Expands the Clinical Spectrum to Atypical Late‐Onset Phenotypes

Efficacy and tolerance of cannabidiol in the treatment of epilepsy in patients with Rett syndrome

Slow Titration of Cannabidiol Add-On in Drug-Resistant Epilepsies Can Improve Safety With Maintained Efficacy in an Open-Label Study

Molecular and clinical descriptions of patients with GABAA receptor gene variants (GABRA1, GABRB2, GABRB3, GABRG2): A cohort study, review of literature, and genotype–phenotype correlation

De novo mutations in CBL causing early-onset paediatric moyamoya angiopathy

What is the optimal duration for vigabatrin monotherapy in patients with infantile spasms: 6 months or longer?

Cognitive outcome in children with infantile spasms using a standardized treatment protocol. A five-year longitudinal study

Pro-epileptogenic effects of viral-like inflammation in both mature and immature brains

Diagnosis delay in West syndrome: misdiagnosis and consequences

Kingella kingae Sequence Type 25 Causing Endocarditis with Multiple and Severe Cerebral Complications

Impact of cardiac surgical timing on the neurodevelopmental outcomes of newborns with Complex congenital heart disease (CHD)

Impacts of an Interdisciplinary Developmental Follow-Up Program on Neurodevelopment in Congenital Heart Disease: The CINC Study

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