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Nouha Essid

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IEEE Transactions on Neural Systems and Rehabilitation Engineering : a Publication of the IEEE Engineering in Medicine and Biology Society|October 2, 2024
Adapting Action Recognition Neural Networks for Automated Infantile Spasm DetectionSamuel Diop, Nouha Essid, Francois Jouen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 20, 2012
Sleep-disordered breathing in children with congenital muscular dystrophiesJean-Marc Pinard, Eric Azabou, Nouha Essid, et al.
American Journal of Medical Genetics. Part A|April 28, 2016
A de novo 10p11.23-p12.1 deletion recapitulates the phenotype observed in WAC mutations and strengthens the role of WAC in intellectual disability and behavior disordersFatma Abdelhedi, Laila El Khattabi, Nouha Essid, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 14, 2012
Sleep architecture impairment in epileptic children and putative role of anti epileptic drugsValentina M Racaru, Fawzia Cheliout-Heraut, Eric Azabou, et al.
Annals of Neurology|May 31, 2017
A simple blood test expedites the diagnosis of glucose transporter type 1 deficiency syndromeDomitille Gras, Christelle Cousin, Caroline Kappeler, et al.
Neurology|April 19, 2023
Prospective Multicenter Validation of a Simple Blood Test for the Diagnosis of Glut1 Deficiency SyndromeFanny Mochel, Domitille Gras, Marie-Pierre Luton, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
IEEE Transactions on Neural Systems and Rehabilitation Engineering : a Publication of the IEEE Engineering in Medicine and Biology Society|October 2, 2024
Adapting Action Recognition Neural Networks for Automated Infantile Spasm DetectionSamuel Diop, Nouha Essid, Francois Jouen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 20, 2012
Sleep-disordered breathing in children with congenital muscular dystrophiesJean-Marc Pinard, Eric Azabou, Nouha Essid, et al.
American Journal of Medical Genetics. Part A|April 28, 2016
A de novo 10p11.23-p12.1 deletion recapitulates the phenotype observed in WAC mutations and strengthens the role of WAC in intellectual disability and behavior disordersFatma Abdelhedi, Laila El Khattabi, Nouha Essid, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 14, 2012
Sleep architecture impairment in epileptic children and putative role of anti epileptic drugsValentina M Racaru, Fawzia Cheliout-Heraut, Eric Azabou, et al.
Annals of Neurology|May 31, 2017
A simple blood test expedites the diagnosis of glucose transporter type 1 deficiency syndromeDomitille Gras, Christelle Cousin, Caroline Kappeler, et al.
Neurology|April 19, 2023
Prospective Multicenter Validation of a Simple Blood Test for the Diagnosis of Glut1 Deficiency SyndromeFanny Mochel, Domitille Gras, Marie-Pierre Luton, et al.
Pageof 1