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Matteo Cataldi

Showing results (11-20 of 24) with videos related to

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Journal of Neuroimmunology|October 11, 2023
Asynchronous combined central and peripheral demyelination (CCPD) in a girl with anti-MOG positivity: A case report and review of the literatureLuca Bosisio, Matteo Gastaldi, Matilde Inglese, et al.
Seizure|March 24, 2019
Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutationMatteo Cataldi, Lino Nobili, Federico Zara, et al.
Neuropediatrics|July 30, 2021
Longitudinally Extensive Transverse Myelitis (LETM) and Myopericarditis in a 7-Month-Old Child with SARs-CoV-2 InfectionGiacomo Brisca, Stefano Sotgiu, Daniela Pirlo, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 19, 2021
Multimodal approach in the pre-surgical evaluation of focal epilepsy surgery candidates: how far are we from a non-invasive ESI-based "sourcectomy"?Giulia Nobile, Alessandro Consales, Domenico Tortora, et al.
Journal of Neurology|September 24, 2021
Correction to: Sleep disturbances in craniopharyngioma: a challenging diagnosisRamona Cordani, Marco Veneruso, Flavia Napoli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 26, 2026
Correction to: Head to head comparison between arterial spin labelling MRI and [18F]FDG-PET in presurgical evaluation of epilepsy in children: the role of voxel-based asymmetry index analysisPietro Mattioli, Giulia Nobile, Matteo Cataldi, et al.
Journal of Neurology|September 15, 2021
Sleep disturbances in craniopharyngioma: a challenging diagnosisRamona Cordani, Marco Veneruso, Flavia Napoli, et al.
Journal of Child Neurology|August 18, 2025
Early-Onset Sensorimotor Axonal Neuropathy as Sole Manifestation of <i>HADHA</i>-Related Disorder/ Mitochondrial Trifunctional Protein DefectGiulia Balletto, Giulia Barbagallo, Matteo Cataldi, et al.
Biomedicines|January 20, 2021
Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in <i>KCNA1</i> Impairing the Voltage Sensitivity of Kv1.1 ChannelPaola Imbrici, Andrea Accogli, Rikard Blunck, et al.
Diagnostics (Basel, Switzerland)|April 23, 2022
Comparison of Qualitative and Quantitative Analyses of MR-Arterial Spin Labeling Perfusion Data for the Assessment of Pediatric Patients with Focal EpilepsiesDomenico Tortora, Matteo Cataldi, Mariasavina Severino, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Journal of Neuroimmunology|October 11, 2023
Asynchronous combined central and peripheral demyelination (CCPD) in a girl with anti-MOG positivity: A case report and review of the literatureLuca Bosisio, Matteo Gastaldi, Matilde Inglese, et al.
Seizure|March 24, 2019
Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutationMatteo Cataldi, Lino Nobili, Federico Zara, et al.
Neuropediatrics|July 30, 2021
Longitudinally Extensive Transverse Myelitis (LETM) and Myopericarditis in a 7-Month-Old Child with SARs-CoV-2 InfectionGiacomo Brisca, Stefano Sotgiu, Daniela Pirlo, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 19, 2021
Multimodal approach in the pre-surgical evaluation of focal epilepsy surgery candidates: how far are we from a non-invasive ESI-based "sourcectomy"?Giulia Nobile, Alessandro Consales, Domenico Tortora, et al.
Journal of Neurology|September 24, 2021
Correction to: Sleep disturbances in craniopharyngioma: a challenging diagnosisRamona Cordani, Marco Veneruso, Flavia Napoli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 26, 2026
Correction to: Head to head comparison between arterial spin labelling MRI and [18F]FDG-PET in presurgical evaluation of epilepsy in children: the role of voxel-based asymmetry index analysisPietro Mattioli, Giulia Nobile, Matteo Cataldi, et al.
Journal of Neurology|September 15, 2021
Sleep disturbances in craniopharyngioma: a challenging diagnosisRamona Cordani, Marco Veneruso, Flavia Napoli, et al.
Journal of Child Neurology|August 18, 2025
Early-Onset Sensorimotor Axonal Neuropathy as Sole Manifestation of <i>HADHA</i>-Related Disorder/ Mitochondrial Trifunctional Protein DefectGiulia Balletto, Giulia Barbagallo, Matteo Cataldi, et al.
Biomedicines|January 20, 2021
Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in <i>KCNA1</i> Impairing the Voltage Sensitivity of Kv1.1 ChannelPaola Imbrici, Andrea Accogli, Rikard Blunck, et al.
Diagnostics (Basel, Switzerland)|April 23, 2022
Comparison of Qualitative and Quantitative Analyses of MR-Arterial Spin Labeling Perfusion Data for the Assessment of Pediatric Patients with Focal EpilepsiesDomenico Tortora, Matteo Cataldi, Mariasavina Severino, et al.
Pageof 3