Publications by authors named "Matteo Cataldi"

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VNS treatment in super-refractory status epilepticus: report of two cases and systematic review of literature.
Luca Bosisio, Giulia Barbagallo, Lino Nobili, Gianluca Piatelli, Mattia Pacetti, Matteo Cataldi

Neurol Sci· November 2025

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Case Report: Parsonage-Turner syndrome due to SEPTIN9 mutation: report of an Italian family with childhood onset and review of the literature.
Luca Bosisio, Matteo Cataldi, Marina Grandis, Barbara Tappino, Monica Traverso

Front Pediatr· September 2025

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Early-Onset Sensorimotor Axonal Neuropathy as Sole Manifestation of -Related Disorder/ Mitochondrial Trifunctional Protein Defect.
Giulia Balletto, Giulia Barbagallo, Matteo Cataldi, Francesco Germano, Monica Traverso

J Child Neurol· August 2025

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Neurophysiological Assessment in Children with Vocal Fold Paralysis: A Tertiary Center Experience.
Roberto D'Agostino, Tommaso Cacco, Ivana Fiz, Mirta Della Rocca, Simona Martelli, Matteo Cataldi

Laryngoscope· February 2025

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Early Onset Inherited Peripheral Neuropathies: The Experience of a Specialized Referral Center for Genetic Diagnosis Achievement.
Alessandro Geroldi, Clarissa Ponti, Alessia Mammi, Serena Patrone, Fabio Gotta, Matteo Cataldi

Pediatr Neurol· May 2024

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Navigating the complexities of encephalocraniocutaneous lipomatosis: a case series and review.
Marco Pavanello, Liliana Piro, Arianna Roggero, Andrea Rossi, Matteo Cataldi

Childs Nerv Syst· April 2024

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A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers.
Alessandro Geroldi, Stefano Tozza, Chiara Fiorillo, Maria Nolano, Paola Fossa, Matteo Cataldi

J Peripher Nerv Syst· December 2023

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Asynchronous combined central and peripheral demyelination (CCPD) in a girl with anti-MOG positivity: A case report and review of the literature.
Luca Bosisio, Matteo Gastaldi, Matilde Inglese, Andrea Rossi, Diego Franciotta, Matteo Cataldi

J Neuroimmunol· November 2023

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Recurrent Sensory-Motor Neuropathy Mimicking CIDP as Predominant Presentation of PDH Deficiency.
Carolina Croci, Matteo Cataldi, Serena Baratto, Claudio Bruno, Federica Trucco

Neuropediatrics· June 2023

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The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatment.
Chiara Fiorillo, Giovanna Capodivento, Alessandro Geroldi, Stefano Tozza, Isabella Moroni, Matteo Cataldi

Neuropathol Appl Neurobiol· December 2022

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On the role of REM sleep microstructure in suppressing interictal spikes in Electrical Status Epilepticus during Sleep.
Thea Giacomini, Gianvittorio Luria, Vanessa D'Amario, Carolina Croci, Matteo Cataldi

Clin Neurophysiol· April 2022

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Comparison of Qualitative and Quantitative Analyses of MR-Arterial Spin Labeling Perfusion Data for the Assessment of Pediatric Patients with Focal Epilepsies.
Domenico Tortora, Matteo Cataldi, Mariasavina Severino, Alessandro Consales, Mattia Pacetti

Diagnostics (Basel)· March 2022

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Longitudinally Extensive Transverse Myelitis (LETM) and Myopericarditis in a 7-Month-Old Child with SARs-CoV-2 Infection.
Giacomo Brisca, Stefano Sotgiu, Daniela Pirlo, Barbara Tubino, Laura Siri, Matteo Cataldi

Neuropediatrics· February 2022

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Sleep disturbances in craniopharyngioma: a challenging diagnosis.
Ramona Cordani, Marco Veneruso, Flavia Napoli, Claudia Milanaccio, Antonio Verrico, Matteo Cataldi

J Neurol· November 2021

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Correction to: Sleep disturbances in craniopharyngioma: a challenging diagnosis.
Ramona Cordani, Marco Veneruso, Flavia Napoli, Claudia Milanaccio, Antonio Verrico, Matteo Cataldi

J Neurol· November 2021

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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, Mattia Pacetti, Francesca Gianno, Matteo Cataldi

Epileptic Disord· August 2021

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Sleep disorders in Prader-Willi syndrome, evidence from animal models and humans.
Matteo Cataldi, Dario Arnaldi, Valter Tucci, Fabrizio De Carli, Giuseppa Patti

Sleep Med Rev· June 2021

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Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in Impairing the Voltage Sensitivity of Kv1.1 Channel.
Paola Imbrici, Andrea Accogli, Rikard Blunck, Concetta Altamura, Michele Iacomino, Matteo Cataldi

Biomedicines· January 2021

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Increased Childhood Peripheral Facial Palsy in the Emergency Department During COVID-19 Pandemic.
Giacomo Brisca, Francesca Garbarino, Sabina Carta, Antonella Palmieri, Marta Vandone, Matteo Cataldi

Pediatr Emerg Care· October 2020

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Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutation.
Matteo Cataldi, Lino Nobili, Federico Zara, Romina Combi, Giulia Prato

Seizure· April 2019

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A novel approach to estimate trabecular bone anisotropy using a database approach.
Javad Hazrati Marangalou, Keita Ito, Matteo Cataldi, Fulvia Taddei, Bert van Rietbergen

J Biomech· September 2013

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