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Jamel Chelly

Showing results (91-100 of 226) with videos related to

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Epilepsy & Behavior : E&B|February 26, 2020
Remarkable effect of transdermal nicotine in children with CHRNA4-related autosomal dominant sleep-related hypermotor epilepsyKristine Lossius, Anne de Saint Martin, Sverre Myren-Svelstad, et al.
Human Mutation|October 17, 2006
Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD geneNathalie Deburgrave, Fatma Daoud, Stéphane Llense, 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.
Pediatric Neurology|May 2, 2006
The incidence of Rett syndrome in FranceThierry Bienvenu, Christophe Philippe, Nicolas De Roux, et al.
The Journal of Pathology|November 5, 2003
Loss of parental-specific methylation at the IGF2 locus in human hepatocellular carcinomaKarine Poirier, Céline Chalas, Frédérique Tissier, 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.
Journal of Neuropathology and Experimental Neurology|April 11, 2017
Neuropathological Hallmarks of Brain Malformations in Extreme Phenotypes Related to DYNC1H1 MutationsAnnie Laquerriere, Camille Maillard, Mara Cavallin, 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.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 31, 2007
Loss of X-linked mental retardation gene oligophrenin1 in mice impairs spatial memory and leads to ventricular enlargement and dendritic spine immaturityMalik Khelfaoui, Cécile Denis, Elly van Galen, 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 23

Showing results (91-100 of 226) with videos related to

Sort By:
Pageof 23
Epilepsy & Behavior : E&B|February 26, 2020
Remarkable effect of transdermal nicotine in children with CHRNA4-related autosomal dominant sleep-related hypermotor epilepsyKristine Lossius, Anne de Saint Martin, Sverre Myren-Svelstad, et al.
Human Mutation|October 17, 2006
Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD geneNathalie Deburgrave, Fatma Daoud, Stéphane Llense, 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.
Pediatric Neurology|May 2, 2006
The incidence of Rett syndrome in FranceThierry Bienvenu, Christophe Philippe, Nicolas De Roux, et al.
The Journal of Pathology|November 5, 2003
Loss of parental-specific methylation at the IGF2 locus in human hepatocellular carcinomaKarine Poirier, Céline Chalas, Frédérique Tissier, 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.
Journal of Neuropathology and Experimental Neurology|April 11, 2017
Neuropathological Hallmarks of Brain Malformations in Extreme Phenotypes Related to DYNC1H1 MutationsAnnie Laquerriere, Camille Maillard, Mara Cavallin, 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.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 31, 2007
Loss of X-linked mental retardation gene oligophrenin1 in mice impairs spatial memory and leads to ventricular enlargement and dendritic spine immaturityMalik Khelfaoui, Cécile Denis, Elly van Galen, 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 23