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Vincent des Portes

Showing results (11-20 of 114) with videos related to

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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 7, 2013
Early diagnosis of pyridoxine-dependent epilepsy: video-EEG monitoring and biochemical and genetic investigationDorothée Ville, Carole Ginguene, Stéphanie Marignier, et al.
Experimental Brain Research|April 26, 2013
Simultaneous action execution and observation optimise grasping actionsMathilde Ménoret, Aurore Curie, Vincent des Portes, et al.
Prenatal Diagnosis|April 25, 2019
Fetal and perinatal outcome associated with small cerebellar diameter based on second- or third-trimester ultrasonographyAnthony Atallah, Laurent Guibaud, Pascal Gaucherand, et al.
European Journal of Medical Genetics|April 19, 2012
Childhood apraxia of speech without intellectual deficit in a patient with cri du chat syndromeStéphanie Marignier, Gaetan Lesca, Jessica Marguin, et al.
Fetal Diagnosis and Therapy|July 14, 2016
Expanding Porencephalic Cysts: Prenatal Imaging and Differential DiagnosisAdva Abergel, Audrey Lacalm, Mona Massoud, et al.
The Journal of Clinical Psychiatry|May 13, 2014
Translating molecular advances in fragile X syndrome into therapy: a reviewRandi J Hagerman, Vincent Des-Portes, Fabrizio Gasparini, et al.
Epilepsy & Behavior : E&B|April 8, 2011
Atypical hemispheric asymmetries for the processing of phonological features in children with rolandic epilepsyNathalie Bedoin, Emmanuel Ferragne, Céline Lopez, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 30, 2020
Early-onset epileptic encephalopathy with migrating focal seizures associated with a FARS2 homozygous nonsense variantDorothée Ville, Gaetan Lesca, Audrey Labalme, et al.
European Journal of Medical Genetics|February 25, 2020
Novel truncating and missense variants extending the spectrum of EMC1-related phenotypes, causing autism spectrum disorder, severe global development delay and visual impairmentSara Cabet, Gaetan Lesca, Audrey Labalme, et al.
Fetal Diagnosis and Therapy|March 8, 2021
Prenatal Imaging Features and Postnatal Outcome of Short Corpus Callosum: A Series of 42 CasesCaroline Bartholmot, Sara Cabet, Mona Massoud, et al.
Pageof 12

Showing results (11-20 of 114) with videos related to

Sort By:
Pageof 12
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 7, 2013
Early diagnosis of pyridoxine-dependent epilepsy: video-EEG monitoring and biochemical and genetic investigationDorothée Ville, Carole Ginguene, Stéphanie Marignier, et al.
Experimental Brain Research|April 26, 2013
Simultaneous action execution and observation optimise grasping actionsMathilde Ménoret, Aurore Curie, Vincent des Portes, et al.
Prenatal Diagnosis|April 25, 2019
Fetal and perinatal outcome associated with small cerebellar diameter based on second- or third-trimester ultrasonographyAnthony Atallah, Laurent Guibaud, Pascal Gaucherand, et al.
European Journal of Medical Genetics|April 19, 2012
Childhood apraxia of speech without intellectual deficit in a patient with cri du chat syndromeStéphanie Marignier, Gaetan Lesca, Jessica Marguin, et al.
Fetal Diagnosis and Therapy|July 14, 2016
Expanding Porencephalic Cysts: Prenatal Imaging and Differential DiagnosisAdva Abergel, Audrey Lacalm, Mona Massoud, et al.
The Journal of Clinical Psychiatry|May 13, 2014
Translating molecular advances in fragile X syndrome into therapy: a reviewRandi J Hagerman, Vincent Des-Portes, Fabrizio Gasparini, et al.
Epilepsy & Behavior : E&B|April 8, 2011
Atypical hemispheric asymmetries for the processing of phonological features in children with rolandic epilepsyNathalie Bedoin, Emmanuel Ferragne, Céline Lopez, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 30, 2020
Early-onset epileptic encephalopathy with migrating focal seizures associated with a FARS2 homozygous nonsense variantDorothée Ville, Gaetan Lesca, Audrey Labalme, et al.
European Journal of Medical Genetics|February 25, 2020
Novel truncating and missense variants extending the spectrum of EMC1-related phenotypes, causing autism spectrum disorder, severe global development delay and visual impairmentSara Cabet, Gaetan Lesca, Audrey Labalme, et al.
Fetal Diagnosis and Therapy|March 8, 2021
Prenatal Imaging Features and Postnatal Outcome of Short Corpus Callosum: A Series of 42 CasesCaroline Bartholmot, Sara Cabet, Mona Massoud, et al.
Pageof 12