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Renzo Guerrini

Showing results (561-570 of 611) with videos related to

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Neurology|June 26, 2025
Phenotypic Spectrum in Individuals With Pathogenic <i>GABRG2</i> Loss- and Gain-of-Function VariantsAlessandra Rossi, Susan X N Lin, Nathan L Absalom, et al.
Neurology|December 5, 2020
Basal Ganglia Dysmorphism in Patients With Aicardi SyndromeSilvia Masnada, Anna Pichiecchio, Manuela Formica, et al.
Brain : a Journal of Neurology|August 14, 2025
Associations between epilepsy-related polygenic risk and brain morphology in childhoodAlexander Ngo, Lang Liu, Sara Larivière, et al.
Neurology|July 22, 2025
Development and Adaptive Function in Individuals With <i>SCN2A</i>-Related DisordersBeatrice Southby Goad, Jill Rodda, Meagan Allen, et al.
Biorxiv : the Preprint Server for Biology|January 27, 2025
ASSOCIATIONS BETWEEN EPILEPSY-RELATED POLYGENIC RISK AND BRAIN MORPHOLOGY IN CHILDHOODAlexander Ngo, Lang Liu, Sara Larivière, et al.
JCI Insight|September 16, 2016
<i>PIK3CA</i>-associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distributionGhayda Mirzaa, Andrew E Timms, Valerio Conti, et al.
Epilepsia|January 17, 2012
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies, Costin Leu, Carolien G F de Kovel, et al.
Epilepsia|September 21, 2020
Developmental and epilepsy spectrum of KCNB1 encephalopathy with long-term outcomeClaire Bar, Mathieu Kuchenbuch, Giulia Barcia, et al.
Epilepsia|November 30, 2021
Atlas of lesion locations and postsurgical seizure freedom in focal cortical dysplasia: A MELD studyKonrad Wagstyl, Kirstie Whitaker, Armin Raznahan, et al.
Brain : a Journal of Neurology|October 24, 2018
HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyondCarla Marini, Alessandro Porro, Agnès Rastetter, et al.
Pageof 62

Showing results (561-570 of 611) with videos related to

Sort By:
Pageof 62
Neurology|June 26, 2025
Phenotypic Spectrum in Individuals With Pathogenic <i>GABRG2</i> Loss- and Gain-of-Function VariantsAlessandra Rossi, Susan X N Lin, Nathan L Absalom, et al.
Neurology|December 5, 2020
Basal Ganglia Dysmorphism in Patients With Aicardi SyndromeSilvia Masnada, Anna Pichiecchio, Manuela Formica, et al.
Brain : a Journal of Neurology|August 14, 2025
Associations between epilepsy-related polygenic risk and brain morphology in childhoodAlexander Ngo, Lang Liu, Sara Larivière, et al.
Neurology|July 22, 2025
Development and Adaptive Function in Individuals With <i>SCN2A</i>-Related DisordersBeatrice Southby Goad, Jill Rodda, Meagan Allen, et al.
Biorxiv : the Preprint Server for Biology|January 27, 2025
ASSOCIATIONS BETWEEN EPILEPSY-RELATED POLYGENIC RISK AND BRAIN MORPHOLOGY IN CHILDHOODAlexander Ngo, Lang Liu, Sara Larivière, et al.
JCI Insight|September 16, 2016
<i>PIK3CA</i>-associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distributionGhayda Mirzaa, Andrew E Timms, Valerio Conti, et al.
Epilepsia|January 17, 2012
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies, Costin Leu, Carolien G F de Kovel, et al.
Epilepsia|September 21, 2020
Developmental and epilepsy spectrum of KCNB1 encephalopathy with long-term outcomeClaire Bar, Mathieu Kuchenbuch, Giulia Barcia, et al.
Epilepsia|November 30, 2021
Atlas of lesion locations and postsurgical seizure freedom in focal cortical dysplasia: A MELD studyKonrad Wagstyl, Kirstie Whitaker, Armin Raznahan, et al.
Brain : a Journal of Neurology|October 24, 2018
HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyondCarla Marini, Alessandro Porro, Agnès Rastetter, et al.
Pageof 62