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Hala Nasser

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Developmental Medicine and Child Neurology|September 7, 2019
Paediatric-onset neuronal ceroid lipofuscinosis: first symptoms and presentation at diagnosisBlandine Dozières-Puyravel, Hala Nasser, Monique Elmaleh-Bergès, et al.
American Journal of Medical Genetics. Part A|April 26, 2017
Phosphoglycerate dehydrogenase (PHGDH) deficiency without epilepsy mimicking primary microcephalyAntoine Poli, Yoann Vial, Damien Haye, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 2, 2023
Real-life data comparing the efficacy of vigabatrin and oral steroids given sequentially or combined for infantile epileptic spasms syndromeBlandine Dozieres-Puyravel, Hala Nasser, François-Xavier Mauvais, et al.
The Journal of Clinical Investigation|July 9, 2011
VIP blockade leads to microcephaly in mice via disruption of Mcph1-Chk1 signalingSandrine Passemard, Vincent El Ghouzzi, Hala Nasser, et al.
Imaging Neuroscience (Cambridge, Mass.)|August 13, 2025
Characterizing the temporal dynamics and maturation of brain activity during sleep: An EEG microstate study in preterm and full-term infantsParvaneh Adibpour, Hala Nasser, Amandine Pedoux, et al.
Developmental Cognitive Neuroscience|July 14, 2026
Characterization of aperiodic and theta activity in preterm infants using EEG: Insights into cerebral maturation and inter-individual variabilityAline González Carpinteiro, Hala Nasser, Amandine Pedoux, et al.
Journal of Medical Genetics|February 5, 2020
<i>CDK5RAP2</i> primary microcephaly is associated with hypothalamic, retinal and cochlear developmental defectsHala Nasser, Liza Vera, Monique Elmaleh-Bergès, et al.
Clinical Genetics|June 27, 2021
EPHA7 haploinsufficiency is associated with a neurodevelopmental disorderJonathan Lévy, Bérénice Schell, Hala Nasser, et al.
European Journal of Human Genetics : EJHG|May 30, 2020
Biallelic PDE2A variants: a new cause of syndromic paroxysmal dyskinesiaDiane Doummar, Christel Dentel, Romane Lyautey, et al.
Cancers|July 2, 2021
Severe Phenotype in Patients with Large Deletions of <i>NF1</i>Laurence Pacot, Dominique Vidaud, Audrey Sabbagh, et al.
Pageof 2

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

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Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Developmental Medicine and Child Neurology|September 7, 2019
Paediatric-onset neuronal ceroid lipofuscinosis: first symptoms and presentation at diagnosisBlandine Dozières-Puyravel, Hala Nasser, Monique Elmaleh-Bergès, et al.
American Journal of Medical Genetics. Part A|April 26, 2017
Phosphoglycerate dehydrogenase (PHGDH) deficiency without epilepsy mimicking primary microcephalyAntoine Poli, Yoann Vial, Damien Haye, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 2, 2023
Real-life data comparing the efficacy of vigabatrin and oral steroids given sequentially or combined for infantile epileptic spasms syndromeBlandine Dozieres-Puyravel, Hala Nasser, François-Xavier Mauvais, et al.
The Journal of Clinical Investigation|July 9, 2011
VIP blockade leads to microcephaly in mice via disruption of Mcph1-Chk1 signalingSandrine Passemard, Vincent El Ghouzzi, Hala Nasser, et al.
Imaging Neuroscience (Cambridge, Mass.)|August 13, 2025
Characterizing the temporal dynamics and maturation of brain activity during sleep: An EEG microstate study in preterm and full-term infantsParvaneh Adibpour, Hala Nasser, Amandine Pedoux, et al.
Developmental Cognitive Neuroscience|July 14, 2026
Characterization of aperiodic and theta activity in preterm infants using EEG: Insights into cerebral maturation and inter-individual variabilityAline González Carpinteiro, Hala Nasser, Amandine Pedoux, et al.
Journal of Medical Genetics|February 5, 2020
<i>CDK5RAP2</i> primary microcephaly is associated with hypothalamic, retinal and cochlear developmental defectsHala Nasser, Liza Vera, Monique Elmaleh-Bergès, et al.
Clinical Genetics|June 27, 2021
EPHA7 haploinsufficiency is associated with a neurodevelopmental disorderJonathan Lévy, Bérénice Schell, Hala Nasser, et al.
European Journal of Human Genetics : EJHG|May 30, 2020
Biallelic PDE2A variants: a new cause of syndromic paroxysmal dyskinesiaDiane Doummar, Christel Dentel, Romane Lyautey, et al.
Cancers|July 2, 2021
Severe Phenotype in Patients with Large Deletions of <i>NF1</i>Laurence Pacot, Dominique Vidaud, Audrey Sabbagh, et al.
Pageof 2