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Developmental Medicine and Child Neurology
|
September 7, 2019
Paediatric-onset neuronal ceroid lipofuscinosis: first symptoms and presentation at diagnosis
Blandine 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 microcephaly
Antoine 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 syndrome
Blandine 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 signaling
Sandrine 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 infants
Parvaneh 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 variability
Aline 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 defects
Hala Nasser, Liza Vera, Monique Elmaleh-Bergès, et al.
Clinical Genetics
|
June 27, 2021
EPHA7 haploinsufficiency is associated with a neurodevelopmental disorder
Jonathan 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 dyskinesia
Diane 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.
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Showing results (11-20 of 20) with videos related to
Sort By:
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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 diagnosis
Blandine 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 microcephaly
Antoine 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 syndrome
Blandine 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 signaling
Sandrine 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 infants
Parvaneh 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 variability
Aline 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 defects
Hala Nasser, Liza Vera, Monique Elmaleh-Bergès, et al.
Clinical Genetics
|
June 27, 2021
EPHA7 haploinsufficiency is associated with a neurodevelopmental disorder
Jonathan 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 dyskinesia
Diane 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.
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