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Renzo Guerrini

Showing results (431-440 of 611) with videos related to

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European Journal of Pediatrics|April 18, 2021
Consensus statements on the information to deliver after a febrile seizureAnna Loussouarn, Anita Devlin, Thomas Bast, et al.
Human Molecular Genetics|November 11, 2008
Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopiaRussell J Ferland, Luis Federico Batiz, Jason Neal, et al.
Clinical Epigenetics|April 20, 2022
Epimutations in both the TESK2 and MMACHC promoters in the Epi-cblC inherited disorder of intracellular metabolism of vitamin B<sub>12</sub>Abderrahim Oussalah, Youssef Siblini, Sébastien Hergalant, et al.
Epilepsy & Behavior : E&B|October 11, 2025
Final analysis from an open-label extension study of fenfluramine for the treatment of seizures in Lennox-Gastaut syndrome: long-term impact on patients and caregiversKelly G Knupp, Ingrid E Scheffer, An-Sofie Schoonjans, et al.
Frontiers in Pharmacology|June 2, 2022
Orphan Drug Use in Patients With Rare Diseases: A Population-Based Cohort StudyFrancesca Gorini, Michele Santoro, Anna Pierini, et al.
Clinical Epigenetics|July 3, 2021
PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutationsCatia Cavicchi, Abderrahim Oussalah, Silvia Falliano, et al.
Journal of Clinical Medicine|August 7, 2021
The Diagnostic Approach to Mitochondrial Disorders in Children in the Era of Next-Generation Sequencing: A 4-Year Cohort StudyDeborah Tolomeo, Daniele Orsucci, Claudia Nesti, et al.
Brain : a Journal of Neurology|April 19, 2018
De novo mutations of the ATP6V1A gene cause developmental encephalopathy with epilepsyAnna Fassio, Alessandro Esposito, Mitsuhiro Kato, et al.
Epilepsia|September 6, 2012
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsyCarla Marini, Francesca Darra, Nicola Specchio, et al.
Epilepsy Research|October 20, 2009
Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14Barry A Chioza, Jean Aicardi, Harald Aschauer, et al.
Pageof 62

Showing results (431-440 of 611) with videos related to

Sort By:
Pageof 62
European Journal of Pediatrics|April 18, 2021
Consensus statements on the information to deliver after a febrile seizureAnna Loussouarn, Anita Devlin, Thomas Bast, et al.
Human Molecular Genetics|November 11, 2008
Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopiaRussell J Ferland, Luis Federico Batiz, Jason Neal, et al.
Clinical Epigenetics|April 20, 2022
Epimutations in both the TESK2 and MMACHC promoters in the Epi-cblC inherited disorder of intracellular metabolism of vitamin B<sub>12</sub>Abderrahim Oussalah, Youssef Siblini, Sébastien Hergalant, et al.
Epilepsy & Behavior : E&B|October 11, 2025
Final analysis from an open-label extension study of fenfluramine for the treatment of seizures in Lennox-Gastaut syndrome: long-term impact on patients and caregiversKelly G Knupp, Ingrid E Scheffer, An-Sofie Schoonjans, et al.
Frontiers in Pharmacology|June 2, 2022
Orphan Drug Use in Patients With Rare Diseases: A Population-Based Cohort StudyFrancesca Gorini, Michele Santoro, Anna Pierini, et al.
Clinical Epigenetics|July 3, 2021
PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutationsCatia Cavicchi, Abderrahim Oussalah, Silvia Falliano, et al.
Journal of Clinical Medicine|August 7, 2021
The Diagnostic Approach to Mitochondrial Disorders in Children in the Era of Next-Generation Sequencing: A 4-Year Cohort StudyDeborah Tolomeo, Daniele Orsucci, Claudia Nesti, et al.
Brain : a Journal of Neurology|April 19, 2018
De novo mutations of the ATP6V1A gene cause developmental encephalopathy with epilepsyAnna Fassio, Alessandro Esposito, Mitsuhiro Kato, et al.
Epilepsia|September 6, 2012
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsyCarla Marini, Francesca Darra, Nicola Specchio, et al.
Epilepsy Research|October 20, 2009
Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14Barry A Chioza, Jean Aicardi, Harald Aschauer, et al.
Pageof 62