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Caterina Garone

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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 14, 2010
A new case of idiopathic hemiplegia hemiconvulsion syndromeEmilio Franzoni, Caterina Garone, Valentina Marchiani, et al.
Methods and Protocols|June 2, 2021
The Transcriptome of SH-SY5Y at Single-Cell Resolution: A CITE-Seq Data Analysis WorkflowDaniele Mercatelli, Nicola Balboni, Francesca De Giorgio, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 15, 2012
Tissue-specific oxidative stress and loss of mitochondria in CoQ-deficient Pdss2 mutant miceCatarina M Quinzii, Caterina Garone, Valentina Emmanuele, et al.
Brain & Development|October 24, 2006
Levetiracetam or oxcarbazepine as monotherapy in newly diagnosed benign epilepsy of childhood with centrotemporal spikes (BECTS): an open-label, parallel group trialGiangennaro Coppola, Emilio Franzoni, Alberto Verrotti, et al.
The Journal of Clinical Investigation|January 28, 2014
Requirement of enhanced Survival Motoneuron protein imposed during neuromuscular junction maturationShingo Kariya, Teresa Obis, Caterina Garone, et al.
Journal of Child Neurology|September 22, 2016
A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement DisorderCaterina Garone, Juliana Gurgel-Giannetti, Simone Sanna-Cherchi, et al.
Journal of Child Neurology|April 25, 2026
Novel Homozygous <i>TUBGCP6</i> Variant Impairs Brain Development: Case Report and Literature ReviewSilvia Lelli, Giulia Balletto, Isabelle Bacchi, et al.
Brain Communications|June 19, 2026
Disease burden of untreated thymidine kinase 2 deficiency: insights from a large patient datasetCristina Domínguez-González, Caterina Garone, Andrés Nascimento, et al.
Seizure|October 22, 2011
Fever as a seizure precipitant factor in Panayiotopoulos syndrome: a clinical and genetic studyDuccio Maria Cordelli, Anna Aldrovandi, Valentina Gentile, et al.
Archives of Neurology|September 12, 2012
MPV17 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA DeletionsCaterina Garone, Juan Carlos Rubio, Sarah E Calvo, et al.
Pageof 6

Showing results (11-20 of 54) with videos related to

Sort By:
Pageof 6
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 14, 2010
A new case of idiopathic hemiplegia hemiconvulsion syndromeEmilio Franzoni, Caterina Garone, Valentina Marchiani, et al.
Methods and Protocols|June 2, 2021
The Transcriptome of SH-SY5Y at Single-Cell Resolution: A CITE-Seq Data Analysis WorkflowDaniele Mercatelli, Nicola Balboni, Francesca De Giorgio, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 15, 2012
Tissue-specific oxidative stress and loss of mitochondria in CoQ-deficient Pdss2 mutant miceCatarina M Quinzii, Caterina Garone, Valentina Emmanuele, et al.
Brain & Development|October 24, 2006
Levetiracetam or oxcarbazepine as monotherapy in newly diagnosed benign epilepsy of childhood with centrotemporal spikes (BECTS): an open-label, parallel group trialGiangennaro Coppola, Emilio Franzoni, Alberto Verrotti, et al.
The Journal of Clinical Investigation|January 28, 2014
Requirement of enhanced Survival Motoneuron protein imposed during neuromuscular junction maturationShingo Kariya, Teresa Obis, Caterina Garone, et al.
Journal of Child Neurology|September 22, 2016
A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement DisorderCaterina Garone, Juliana Gurgel-Giannetti, Simone Sanna-Cherchi, et al.
Journal of Child Neurology|April 25, 2026
Novel Homozygous <i>TUBGCP6</i> Variant Impairs Brain Development: Case Report and Literature ReviewSilvia Lelli, Giulia Balletto, Isabelle Bacchi, et al.
Brain Communications|June 19, 2026
Disease burden of untreated thymidine kinase 2 deficiency: insights from a large patient datasetCristina Domínguez-González, Caterina Garone, Andrés Nascimento, et al.
Seizure|October 22, 2011
Fever as a seizure precipitant factor in Panayiotopoulos syndrome: a clinical and genetic studyDuccio Maria Cordelli, Anna Aldrovandi, Valentina Gentile, et al.
Archives of Neurology|September 12, 2012
MPV17 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA DeletionsCaterina Garone, Juan Carlos Rubio, Sarah E Calvo, et al.
Pageof 6