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Renzo Guerrini

Showing results (411-420 of 611) with videos related to

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Epilepsy Research|June 21, 2007
Linkage and mutational analysis of CLCN2 in childhood absence epilepsyKate Everett, Barry Chioza, Jean Aicardi, et al.
The Journal of Experimental Medicine|July 9, 2020
Mutations in the exocyst component EXOC2 cause severe defects in human brain developmentNicole J Van Bergen, Syed Mukhtar Ahmed, Felicity Collins, et al.
Brain : a Journal of Neurology|April 3, 2023
Widespread genomic influences on phenotype in Dravet syndrome, a 'monogenic' conditionHelena Martins Custodio, Lisa M Clayton, Ravishankara Bellampalli, et al.
Seizure|February 23, 2021
Angiocentric glioma-associated seizures: The possible role of EATT2, pyruvate carboxylase and glutamine synthetaseAnna Maria Buccoliero, Chiara Caporalini, Mirko Scagnet, et al.
Seizure|July 6, 2021
Corrigendum to 'Angiocentric glioma-associated seizures: The possible role of EATT2, pyruvate carboxylase and glutamine synthetase [Seizure: European Journal of Epilepsy 86 (2021) 152-154]Anna Maria Buccoliero, Chiara Caporalini, Mirko Scagnet, et al.
Haematologica|November 27, 2025
Neurodegenerative Langerhans cell histiocytosis: long-term follow-up of 63 patients from the Italian RegistryIrene Trambusti, Francesco Pegoraro, Maria Luisa Coniglio, et al.
Genes|July 2, 2021
Whole Exome Sequencing Is the Minimal Technological Approach in Probands Born to Consanguineous CouplesFrancesca Peluso, Stefano Giuseppe Caraffi, Roberta Zuntini, et al.
Human Molecular Genetics|May 6, 2014
Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotypeElena Ambrosini, Federico Sicca, Maria S Brignone, et al.
Journal of Visualized Experiments : Jove|December 30, 2017
A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain MalformationsValerio Conti, Aurelie Carabalona, Emilie Pallesi-Pocachard, et al.
Epilepsia|October 5, 2022
Fenfluramine provides clinically meaningful reduction in frequency of drop seizures in patients with Lennox-Gastaut syndrome: Interim analysis of an open-label extension studyKelly G Knupp, Ingrid E Scheffer, Berten Ceulemans, et al.
Pageof 62

Showing results (411-420 of 611) with videos related to

Sort By:
Pageof 62
Epilepsy Research|June 21, 2007
Linkage and mutational analysis of CLCN2 in childhood absence epilepsyKate Everett, Barry Chioza, Jean Aicardi, et al.
The Journal of Experimental Medicine|July 9, 2020
Mutations in the exocyst component EXOC2 cause severe defects in human brain developmentNicole J Van Bergen, Syed Mukhtar Ahmed, Felicity Collins, et al.
Brain : a Journal of Neurology|April 3, 2023
Widespread genomic influences on phenotype in Dravet syndrome, a 'monogenic' conditionHelena Martins Custodio, Lisa M Clayton, Ravishankara Bellampalli, et al.
Seizure|February 23, 2021
Angiocentric glioma-associated seizures: The possible role of EATT2, pyruvate carboxylase and glutamine synthetaseAnna Maria Buccoliero, Chiara Caporalini, Mirko Scagnet, et al.
Seizure|July 6, 2021
Corrigendum to 'Angiocentric glioma-associated seizures: The possible role of EATT2, pyruvate carboxylase and glutamine synthetase [Seizure: European Journal of Epilepsy 86 (2021) 152-154]Anna Maria Buccoliero, Chiara Caporalini, Mirko Scagnet, et al.
Haematologica|November 27, 2025
Neurodegenerative Langerhans cell histiocytosis: long-term follow-up of 63 patients from the Italian RegistryIrene Trambusti, Francesco Pegoraro, Maria Luisa Coniglio, et al.
Genes|July 2, 2021
Whole Exome Sequencing Is the Minimal Technological Approach in Probands Born to Consanguineous CouplesFrancesca Peluso, Stefano Giuseppe Caraffi, Roberta Zuntini, et al.
Human Molecular Genetics|May 6, 2014
Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotypeElena Ambrosini, Federico Sicca, Maria S Brignone, et al.
Journal of Visualized Experiments : Jove|December 30, 2017
A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain MalformationsValerio Conti, Aurelie Carabalona, Emilie Pallesi-Pocachard, et al.
Epilepsia|October 5, 2022
Fenfluramine provides clinically meaningful reduction in frequency of drop seizures in patients with Lennox-Gastaut syndrome: Interim analysis of an open-label extension studyKelly G Knupp, Ingrid E Scheffer, Berten Ceulemans, et al.
Pageof 62