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Annals of Clinical and Translational Neurology
|
August 9, 2019
Impaired glycinergic transmission in hyperekplexia: a model of parasomnia overlap disorder
Régis Lopez, François Rivier, Jamel Chelly, et al.
European Journal of Human Genetics : EJHG
|
May 25, 2006
Genetics and pathophysiology of mental retardation
Jamel Chelly, Malik Khelfaoui, Fiona Francis, et al.
Journal of Human Genetics
|
December 3, 2010
An isoform of the severe encephalopathy-related CDKL5 gene, including a novel exon with extremely high sequence conservation, is specifically expressed in brain
Yann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
FEBS Letters
|
December 15, 2012
MeCP2 deficiency is associated with impaired microtubule stability
Chloé Delépine, Juliette Nectoux, Nadia Bahi-Buisson, et al.
The European Journal of Neuroscience
|
March 8, 2006
The role of ARX in cortical development
Gaëlle Friocourt, Karine Poirier, Sonja Rakić, et al.
Developmental Neuroscience
|
December 14, 2007
Alternative transcripts of Dclk1 and Dclk2 and their expression in doublecortin knockout mice
Françoise Phan Dinh Tuy, Yoann Saillour, Caroline Kappeler, et al.
Plos One
|
July 14, 2010
Synaptic maturation at cortical projections to the lateral amygdala in a mouse model of Rett syndrome
Frédéric Gambino, Malik Khelfaoui, Bernard Poulain, et al.
Journal of the Neurological Sciences
|
June 23, 2019
A novel heterozygous ANO3 mutation responsible for myoclonic dystonia
Chloé Laurencin, Emmanuel Broussolle, Teodor Danaila, et al.
American Journal of Medical Genetics. Part A
|
July 6, 2010
Somatic mosaicism for a CDKL5 mutation as an epileptic encephalopathy in males
Julien Masliah-Plachon, Stéphane Auvin, Juliette Nectoux, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
May 24, 2003
Doublecortin functions at the extremities of growing neuronal processes
Gaëlle Friocourt, Annette Koulakoff, Philippe Chafey, et al.
Page
of 23
Search research articles
Search
Showing results (11-20 of 226) with videos related to
Sort By:
Page
of 23
Annals of Clinical and Translational Neurology
|
August 9, 2019
Impaired glycinergic transmission in hyperekplexia: a model of parasomnia overlap disorder
Régis Lopez, François Rivier, Jamel Chelly, et al.
European Journal of Human Genetics : EJHG
|
May 25, 2006
Genetics and pathophysiology of mental retardation
Jamel Chelly, Malik Khelfaoui, Fiona Francis, et al.
Journal of Human Genetics
|
December 3, 2010
An isoform of the severe encephalopathy-related CDKL5 gene, including a novel exon with extremely high sequence conservation, is specifically expressed in brain
Yann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
FEBS Letters
|
December 15, 2012
MeCP2 deficiency is associated with impaired microtubule stability
Chloé Delépine, Juliette Nectoux, Nadia Bahi-Buisson, et al.
The European Journal of Neuroscience
|
March 8, 2006
The role of ARX in cortical development
Gaëlle Friocourt, Karine Poirier, Sonja Rakić, et al.
Developmental Neuroscience
|
December 14, 2007
Alternative transcripts of Dclk1 and Dclk2 and their expression in doublecortin knockout mice
Françoise Phan Dinh Tuy, Yoann Saillour, Caroline Kappeler, et al.
Plos One
|
July 14, 2010
Synaptic maturation at cortical projections to the lateral amygdala in a mouse model of Rett syndrome
Frédéric Gambino, Malik Khelfaoui, Bernard Poulain, et al.
Journal of the Neurological Sciences
|
June 23, 2019
A novel heterozygous ANO3 mutation responsible for myoclonic dystonia
Chloé Laurencin, Emmanuel Broussolle, Teodor Danaila, et al.
American Journal of Medical Genetics. Part A
|
July 6, 2010
Somatic mosaicism for a CDKL5 mutation as an epileptic encephalopathy in males
Julien Masliah-Plachon, Stéphane Auvin, Juliette Nectoux, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
May 24, 2003
Doublecortin functions at the extremities of growing neuronal processes
Gaëlle Friocourt, Annette Koulakoff, Philippe Chafey, et al.
Page
of 23