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Mathieu Milh

Showing results (11-20 of 138) with videos related to

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European Journal of Medical Genetics|March 5, 2013
Mosaic 15q13.3 deletion including CHRNA7 gene in monozygotic twinsCornel Popovici, Tiffany Busa, Chantal Missirian, et al.
The Journal of Physiology|September 30, 2006
Cell domain-dependent changes in the glutamatergic and GABAergic drives during epileptogenesis in the rat CA1 regionLynda El-Hassar, Mathieu Milh, Fabrice Wendling, et al.
European Journal of Human Genetics : EJHG|July 16, 2015
Early-onset epileptic encephalopathy as the initial clinical presentation of WDR45 deletion in a male patientAffef Abidi, Cécile Mignon-Ravix, Pierre Cacciagli, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|September 19, 2025
Fulminant idiopathic intracranial hypertension mimicking Chiari I malformation in a pediatric patient: diagnostic value of MRI and promising outcomes with venous sinus stentingManel Krouma, Basile Kerleroux, Beatrice Desnous, et al.
Cerebral Cortex (New York, N.Y. : 1991)|September 5, 2006
Rapid cortical oscillations and early motor activity in premature human neonateMathieu Milh, Anna Kaminska, Catherine Huon, et al.
Epilepsia|November 26, 2003
Effects of antiepileptic drugs on refractory seizures in the intact immature corticohippocampal formation in vitroPascale Paule Quilichini, Diabé Diabira, Catherine Chiron, et al.
Epilepsy & Behavior : E&B|July 13, 2019
Screening for depression in youth with epilepsy: Psychometric analysis of NDDI-E-Y and NDDI-E in a French populationMarine Viellard, Nathalie Villeneuve, Mathieu Milh, et al.
Epilepsia|October 29, 2018
Screening for depression in youth with epilepsy: The NDDI-E-YAileen McGonigal, Jean-Arthur Micoulaud-Franchi, Nathalie Villeneuve, et al.
Pediatrics|August 21, 2013
Diagnosis and outcome of SCN4A-related severe neonatal episodic laryngospasm (SNEL): 2 new casesEmilie Caietta, Mathieu Milh, Damien Sternberg, et al.
Epilepsy & Behavior : E&B|January 14, 2014
Cognitive and adaptive evaluation of 21 consecutive patients with Dravet syndromeNathalie Villeneuve, Virginie Laguitton, Marine Viellard, et al.
Pageof 14

Showing results (11-20 of 138) with videos related to

Sort By:
Pageof 14
European Journal of Medical Genetics|March 5, 2013
Mosaic 15q13.3 deletion including CHRNA7 gene in monozygotic twinsCornel Popovici, Tiffany Busa, Chantal Missirian, et al.
The Journal of Physiology|September 30, 2006
Cell domain-dependent changes in the glutamatergic and GABAergic drives during epileptogenesis in the rat CA1 regionLynda El-Hassar, Mathieu Milh, Fabrice Wendling, et al.
European Journal of Human Genetics : EJHG|July 16, 2015
Early-onset epileptic encephalopathy as the initial clinical presentation of WDR45 deletion in a male patientAffef Abidi, Cécile Mignon-Ravix, Pierre Cacciagli, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|September 19, 2025
Fulminant idiopathic intracranial hypertension mimicking Chiari I malformation in a pediatric patient: diagnostic value of MRI and promising outcomes with venous sinus stentingManel Krouma, Basile Kerleroux, Beatrice Desnous, et al.
Cerebral Cortex (New York, N.Y. : 1991)|September 5, 2006
Rapid cortical oscillations and early motor activity in premature human neonateMathieu Milh, Anna Kaminska, Catherine Huon, et al.
Epilepsia|November 26, 2003
Effects of antiepileptic drugs on refractory seizures in the intact immature corticohippocampal formation in vitroPascale Paule Quilichini, Diabé Diabira, Catherine Chiron, et al.
Epilepsy & Behavior : E&B|July 13, 2019
Screening for depression in youth with epilepsy: Psychometric analysis of NDDI-E-Y and NDDI-E in a French populationMarine Viellard, Nathalie Villeneuve, Mathieu Milh, et al.
Epilepsia|October 29, 2018
Screening for depression in youth with epilepsy: The NDDI-E-YAileen McGonigal, Jean-Arthur Micoulaud-Franchi, Nathalie Villeneuve, et al.
Pediatrics|August 21, 2013
Diagnosis and outcome of SCN4A-related severe neonatal episodic laryngospasm (SNEL): 2 new casesEmilie Caietta, Mathieu Milh, Damien Sternberg, et al.
Epilepsy & Behavior : E&B|January 14, 2014
Cognitive and adaptive evaluation of 21 consecutive patients with Dravet syndromeNathalie Villeneuve, Virginie Laguitton, Marine Viellard, et al.
Pageof 14