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Elena Parrini

Showing results (1-10 of 82) with videos related to

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Neurobiology of Disease|February 28, 2009
Neuronal migration disordersRenzo Guerrini, Elena Parrini
Epilepsia|September 25, 2012
Epilepsy in Rett syndrome, and CDKL5- and FOXG1-gene-related encephalopathiesRenzo Guerrini, Elena Parrini
Epilepsy & Behavior : E&B|July 14, 2019
What is the role of next generation sequencing in status epilepticus?Renzo Guerrini, Elena Parrini, Carla Marini, et al.
Molecular Diagnosis & Therapy|February 16, 2017
The Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Epilepsy in Paediatric PatientsDavide Mei, Elena Parrini, Carla Marini, et al.
Molecular Syndromology|October 27, 2016
Genetic Basis of Brain MalformationsElena Parrini, Valerio Conti, William B Dobyns, et al.
Neurogenetics|October 2, 2004
Mosaic mutations of the FLN1 gene cause a mild phenotype in patients with periventricular heterotopiaElena Parrini, Davide Mei, Micheal Wright, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 27, 2019
Lesional and non-lesional epilepsies: A blurring genetic boundaryRenzo Guerrini, Elena Parrini, Alessandro Esposito, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 5, 2021
Cerebellar dentate nuclei swelling: a new and early magnetic resonance imaging finding of beta-propeller protein-associated neurodegenerationAlessandra D'Amico, Alfonso Romano, Elena Parrini, et al.
Molecular Genetics & Genomic Medicine|May 7, 2019
Severe presentation and complex brain malformations in an individual carrying a CCND2 variantGerarda Cappuccio, Lorenzo Ugga, Elena Parrini, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 3, 2023
Autism and mild epilepsy associated with a de novo missense pathogenic variant in the GTPase effector domain of DNM1Davide Mei, Elena Parrini, Claudia Bianchini, et al.
Pageof 9

Showing results (1-10 of 82) with videos related to

Sort By:
Pageof 9
Neurobiology of Disease|February 28, 2009
Neuronal migration disordersRenzo Guerrini, Elena Parrini
Epilepsia|September 25, 2012
Epilepsy in Rett syndrome, and CDKL5- and FOXG1-gene-related encephalopathiesRenzo Guerrini, Elena Parrini
Epilepsy & Behavior : E&B|July 14, 2019
What is the role of next generation sequencing in status epilepticus?Renzo Guerrini, Elena Parrini, Carla Marini, et al.
Molecular Diagnosis & Therapy|February 16, 2017
The Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Epilepsy in Paediatric PatientsDavide Mei, Elena Parrini, Carla Marini, et al.
Molecular Syndromology|October 27, 2016
Genetic Basis of Brain MalformationsElena Parrini, Valerio Conti, William B Dobyns, et al.
Neurogenetics|October 2, 2004
Mosaic mutations of the FLN1 gene cause a mild phenotype in patients with periventricular heterotopiaElena Parrini, Davide Mei, Micheal Wright, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 27, 2019
Lesional and non-lesional epilepsies: A blurring genetic boundaryRenzo Guerrini, Elena Parrini, Alessandro Esposito, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 5, 2021
Cerebellar dentate nuclei swelling: a new and early magnetic resonance imaging finding of beta-propeller protein-associated neurodegenerationAlessandra D'Amico, Alfonso Romano, Elena Parrini, et al.
Molecular Genetics & Genomic Medicine|May 7, 2019
Severe presentation and complex brain malformations in an individual carrying a CCND2 variantGerarda Cappuccio, Lorenzo Ugga, Elena Parrini, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 3, 2023
Autism and mild epilepsy associated with a de novo missense pathogenic variant in the GTPase effector domain of DNM1Davide Mei, Elena Parrini, Claudia Bianchini, et al.
Pageof 9