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Early patterns of activity in the developing cortex: Focus on the sensorimotor system

Seminars in cell & developmental biology, 2018-04, Vol.76, p.120-129

2018

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The repertoire of seizure onset patterns in human focal epilepsies: Determinants and prognostic values

Epilepsia (Copenhagen), 2019-01, Vol.60 (1), p.85-95

2019

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Relationship between PET metabolism and SEEG epileptogenicity in focal lesional epilepsy

European journal of nuclear medicine and molecular imaging, 2020-12, Vol.47 (13), p.3130-3142

2020

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Rapid Cortical Oscillations and Early Motor Activity in Premature Human Neonate

Cerebral cortex (New York, N.Y. 1991), 2007-07, Vol.17 (7), p.1582-1594

2007

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A Conserved Switch in Sensory Processing Prepares Developing Neocortex for Vision

Neuron (Cambridge, Mass.), 2010-08, Vol.67 (3), p.480-498

2010

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Prenatal exome sequencing in 65 fetuses with abnormality of the corpus callosum: contribution to further diagnostic delineation

Genetics in medicine, 2020-11, Vol.22 (11), p.1887-1891

2020

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The role of stereoelectroencephalography (SEEG) in reevaluation of epilepsy surgery failures

Epilepsy & behavior, 2018-04, Vol.81, p.86-93

2018

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Early-onset epileptic encephalopathy as the initial clinical presentation of WDR45 deletion in a male patient

European journal of human genetics : EJHG, 2016-04, Vol.24 (4), p.615-618

2016

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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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Auditory stimuli mimicking ambient sounds drive temporal "delta-brushes" in premature infants

PloS one, 2013-11, Vol.8 (11), p.e79028-e79028

2013

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Parents' experiences of parenting a child with profound intellectual and multiple disabilities in France: A qualitative study

Health expectations : an international journal of public participation in health care and health policy, 2024-02, Vol.27 (1), p.e13910-n/a

2024

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Consensus statements on the information to deliver after a febrile seizure

European journal of pediatrics, 2021-09, Vol.180 (9), p.2993-2999

2021

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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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Première crise épileptique chez l’enfant

La Presse Médicale Formation, 2024-04, Vol.5 (2), p.165-167

Milh, Mathieu

2024

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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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Objective Evaluation of Clinical Actionability for Genes Involved in Myopathies: 63 Genes with a Medical Value for Patient Care

International journal of molecular sciences, 2022-08, Vol.23 (15), p.8506

2022

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Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations

Brain & development (Tokyo. 1979), 2018-10, Vol.40 (9), p.768-774

2018

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Tailored suprainsular partial hemispherotomy: a new functional disconnection technique for stroke-induced refractory epilepsy

Journal of neurosurgery. Pediatrics, 2018-12, Vol.22 (6), p.601-609

2018

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Spectrum of pontocerebellar hypoplasia in 13 girls and boys with CASK mutations: confirmation of a recognizable phenotype and first description of a male mosaic patient

Orphanet journal of rare diseases, 2012-03, Vol.7 (1), p.18-18

2012

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Clinical and allelic heterogeneity in a pediatric cohort of 11 patients carrying MFN2 mutation

Brain & development (Tokyo. 1979), 2016-05, Vol.38 (5), p.498-506

2016

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Cell domain-dependent changes in the glutamatergic and GABAergic drives during epileptogenesis in the rat CA1 region

The Journal of physiology, 2007-01, Vol.578 (1), p.193-211

2007

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Early patterns of activity in the developing cortex: Focus on the sensorimotor system

The repertoire of seizure onset patterns in human focal epilepsies: Determinants and prognostic values

Relationship between PET metabolism and SEEG epileptogenicity in focal lesional epilepsy

Rapid Cortical Oscillations and Early Motor Activity in Premature Human Neonate

A Conserved Switch in Sensory Processing Prepares Developing Neocortex for Vision

Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes

Prenatal exome sequencing in 65 fetuses with abnormality of the corpus callosum: contribution to further diagnostic delineation

The role of stereoelectroencephalography (SEEG) in reevaluation of epilepsy surgery failures

Early-onset epileptic encephalopathy as the initial clinical presentation of WDR45 deletion in a male patient

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

Defining the phenotype of FHF1 developmental and epileptic encephalopathy

Auditory stimuli mimicking ambient sounds drive temporal "delta-brushes" in premature infants

Parents' experiences of parenting a child with profound intellectual and multiple disabilities in France: A qualitative study

Consensus statements on the information to deliver after a febrile seizure

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

A recurrent KCNQ2 pore mutation causing early onset epileptic encephalopathy has a moderate effect on M current but alters subcellular localization of Kv7 channels

Première crise épileptique chez l’enfant

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

Objective Evaluation of Clinical Actionability for Genes Involved in Myopathies: 63 Genes with a Medical Value for Patient Care

Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations

KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism

Tailored suprainsular partial hemispherotomy: a new functional disconnection technique for stroke-induced refractory epilepsy

Spectrum of pontocerebellar hypoplasia in 13 girls and boys with CASK mutations: confirmation of a recognizable phenotype and first description of a male mosaic patient

Clinical and allelic heterogeneity in a pediatric cohort of 11 patients carrying MFN2 mutation

Cell domain-dependent changes in the glutamatergic and GABAergic drives during epileptogenesis in the rat CA1 region

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