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Renzo Guerrini

Showing results (481-490 of 611) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|April 27, 2021
Real-life survey of pitfalls and successes of precision medicine in genetic epilepsiesSimona Balestrini, Daniela Chiarello, Maria Gogou, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2022
The Genetic Landscape of Complex Childhood-Onset Hyperkinetic Movement DisordersBelén Pérez-Dueñas, Kathleen Gorman, Anna Marcé-Grau, et al.
Nature Reviews. Neurology|September 8, 2020
International consensus recommendations on the diagnostic work-up for malformations of cortical developmentRenske Oegema, Tahsin Stefan Barakat, Martina Wilke, et al.
Epilepsia|January 31, 2013
Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significanceFederico Zara, Nicola Specchio, Pasquale Striano, et al.
Molecular Genetics & Genomic Medicine|September 22, 2016
Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patientsCarolien G F de Kovel, Eva H Brilstra, Marjan J A van Kempen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 5, 2025
COL4A1 and COL4A2-related disorders: Clinical features, diagnostic guidelines, and managementDiana Tambala, Rachel Vassar, John Snow, et al.
BMJ Open|June 18, 2016
Efficacy of ketamine in refractory convulsive status epilepticus in children: a protocol for a sequential design, multicentre, randomised, controlled, open-label, non-profit trial (KETASER01)Anna Rosati, Lucrezia Ilvento, Manuela L'Erario, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformationNathaniel H Robin, Clare J Taylor, Donna M McDonald-McGinn, et al.
Epilepsia|May 30, 2020
Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizuresShan Tang, Laura Addis, Anna Smith, et al.
Brain : a Journal of Neurology|June 30, 2022
Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disordersNataliya Di Donato, Renzo Guerrini, Charles J Billington, et al.
Pageof 62

Showing results (481-490 of 611) with videos related to

Sort By:
Pageof 62
Journal of Neurology, Neurosurgery, and Psychiatry|April 27, 2021
Real-life survey of pitfalls and successes of precision medicine in genetic epilepsiesSimona Balestrini, Daniela Chiarello, Maria Gogou, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2022
The Genetic Landscape of Complex Childhood-Onset Hyperkinetic Movement DisordersBelén Pérez-Dueñas, Kathleen Gorman, Anna Marcé-Grau, et al.
Nature Reviews. Neurology|September 8, 2020
International consensus recommendations on the diagnostic work-up for malformations of cortical developmentRenske Oegema, Tahsin Stefan Barakat, Martina Wilke, et al.
Epilepsia|January 31, 2013
Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significanceFederico Zara, Nicola Specchio, Pasquale Striano, et al.
Molecular Genetics & Genomic Medicine|September 22, 2016
Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patientsCarolien G F de Kovel, Eva H Brilstra, Marjan J A van Kempen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 5, 2025
COL4A1 and COL4A2-related disorders: Clinical features, diagnostic guidelines, and managementDiana Tambala, Rachel Vassar, John Snow, et al.
BMJ Open|June 18, 2016
Efficacy of ketamine in refractory convulsive status epilepticus in children: a protocol for a sequential design, multicentre, randomised, controlled, open-label, non-profit trial (KETASER01)Anna Rosati, Lucrezia Ilvento, Manuela L'Erario, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformationNathaniel H Robin, Clare J Taylor, Donna M McDonald-McGinn, et al.
Epilepsia|May 30, 2020
Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizuresShan Tang, Laura Addis, Anna Smith, et al.
Brain : a Journal of Neurology|June 30, 2022
Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disordersNataliya Di Donato, Renzo Guerrini, Charles J Billington, et al.
Pageof 62