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Yoann Saillour

Showing results (11-20 of 41) with videos related to

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Brain Research. Molecular Brain Research|March 3, 2004
Neuroanatomical distribution of ARX in brain and its localisation in GABAergic neuronsKarine Poirier, Hilde Van Esch, Gaëlle Friocourt, et al.
Neurogenetics|September 28, 2013
Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyriaStéphanie Valence, Karine Poirier, Nicolas Lebrun, et al.
Development (Cambridge, England)|April 10, 2025
Differential contribution of P73+ Cajal-Retzius cells and Reelin to cortical morphogenesisVicente Elorriaga, Benoît Bouloudi, Elodie Delberghe, et al.
European Journal of Medical Genetics|January 7, 2016
De novo TUBB2B mutation causes fetal akinesia deformation sequence with microlissencephaly: An unusual presentation of tubulinopathyAnnie Laquerriere, Marie Gonzales, Yoann Saillour, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 4, 2017
The X-Linked Intellectual Disability Protein IL1RAPL1 Regulates Dendrite ComplexityCaterina Montani, Mariana Ramos-Brossier, Luisa Ponzoni, et al.
Neurogenetics|October 2, 2009
A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardationGinevra Zanni, Hilde van Esch, Anissa Bensalem, et al.
European Journal of Human Genetics : EJHG|September 6, 2012
Expanding the spectrum of TUBA1A-related cortical dysgenesis to PolymicrogyriaKarine Poirier, Yoann Saillour, Franck Fourniol, et al.
Neurogenetics|July 27, 2012
Mosaic DCX deletion causes subcortical band heterotopia in malesChloé Quélin, Yoann Saillour, Isabelle Souville, et al.
Human Mutation|August 7, 2008
Detection of exonic copy-number changes using a highly efficient oligonucleotide-based comparative genomic hybridization-array methodYoann Saillour, Mireille Cossée, France Leturcq, et al.
Epilepsy Research|May 13, 2008
Combination of infantile spasms, non-epileptic seizures and complex movement disorder: a new case of ARX-related epilepsyKarine Poirier, Monika Eisermann, Isabelle Caubel, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Brain Research. Molecular Brain Research|March 3, 2004
Neuroanatomical distribution of ARX in brain and its localisation in GABAergic neuronsKarine Poirier, Hilde Van Esch, Gaëlle Friocourt, et al.
Neurogenetics|September 28, 2013
Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyriaStéphanie Valence, Karine Poirier, Nicolas Lebrun, et al.
Development (Cambridge, England)|April 10, 2025
Differential contribution of P73+ Cajal-Retzius cells and Reelin to cortical morphogenesisVicente Elorriaga, Benoît Bouloudi, Elodie Delberghe, et al.
European Journal of Medical Genetics|January 7, 2016
De novo TUBB2B mutation causes fetal akinesia deformation sequence with microlissencephaly: An unusual presentation of tubulinopathyAnnie Laquerriere, Marie Gonzales, Yoann Saillour, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 4, 2017
The X-Linked Intellectual Disability Protein IL1RAPL1 Regulates Dendrite ComplexityCaterina Montani, Mariana Ramos-Brossier, Luisa Ponzoni, et al.
Neurogenetics|October 2, 2009
A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardationGinevra Zanni, Hilde van Esch, Anissa Bensalem, et al.
European Journal of Human Genetics : EJHG|September 6, 2012
Expanding the spectrum of TUBA1A-related cortical dysgenesis to PolymicrogyriaKarine Poirier, Yoann Saillour, Franck Fourniol, et al.
Neurogenetics|July 27, 2012
Mosaic DCX deletion causes subcortical band heterotopia in malesChloé Quélin, Yoann Saillour, Isabelle Souville, et al.
Human Mutation|August 7, 2008
Detection of exonic copy-number changes using a highly efficient oligonucleotide-based comparative genomic hybridization-array methodYoann Saillour, Mireille Cossée, France Leturcq, et al.
Epilepsy Research|May 13, 2008
Combination of infantile spasms, non-epileptic seizures and complex movement disorder: a new case of ARX-related epilepsyKarine Poirier, Monika Eisermann, Isabelle Caubel, et al.
Pageof 5