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Matteo Cataldi
Matteo Cataldi
Verified email at studenti.unige.it
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Year
Sleep disorders in Prader-Willi syndrome, evidence from animal models and humans
M Cataldi, D Arnaldi, V Tucci, F De Carli, G Patti, F Napoli, M Pace, ...
Sleep Medicine Reviews 57, 101432, 2021
212021
Increased childhood peripheral facial palsy in the emergency department during COVID-19 pandemic
G Brisca, F Garbarino, S Carta, A Palmieri, M Vandone, M Severino, ...
Pediatric Emergency Care 36 (10), e595-e596, 2020
212020
Longitudinally extensive transverse myelitis (LETM) and myopericarditis in a 7-month-old child with SARs-CoV-2 infection
G Brisca, S Sotgiu, D Pirlo, B Tubino, L Siri, B Chianucci, A Carta, A Rossi, ...
Neuropediatrics 53 (01), 061-064, 2022
132022
Migrating focal seizures in autosomal dominant sleep-related hypermotor epilepsy with KCNT1 mutation
M Cataldi, L Nobili, F Zara, R Combi, G Prato, T Giacomini, V Capra, ...
Seizure 67, 57-60, 2019
122019
On the role of REM sleep microstructure in suppressing interictal spikes in Electrical Status Epilepticus during Sleep
T Giacomini, G Luria, V D’Amario, C Croci, M Cataldi, M Piai, G Nobile, ...
Clinical Neurophysiology 136, 62-68, 2022
112022
Sleep disturbances in craniopharyngioma: a challenging diagnosis
R Cordani, M Veneruso, F Napoli, C Milanaccio, A Verrico, A Consales, ...
Journal of neurology 268, 4362-4369, 2021
112021
The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatment
C Fiorillo, G Capodivento, A Geroldi, S Tozza, I Moroni, P Mohassel, ...
Neuropathology and Applied Neurobiology 48 (7), e12842, 2022
52022
Comparison of qualitative and quantitative analyses of MR-arterial spin labeling perfusion data for the assessment of pediatric patients with focal epilepsies
D Tortora, M Cataldi, M Severino, A Consales, M Pacetti, C Parodi, ...
Diagnostics 12 (4), 811, 2022
52022
Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in KCNA1 Impairing the Voltage Sensitivity of Kv1.1 Channel
P Imbrici, A Accogli, R Blunck, C Altamura, M Iacomino, MC D’adamo, ...
Biomedicines 9 (1), 75, 2021
52021
Asynchronous combined central and peripheral demyelination (CCPD) in a girl with anti-MOG positivity: A case report and review of the literature
L Bosisio, M Gastaldi, M Inglese, A Rossi, D Franciotta, M Cataldi, ...
Journal of Neuroimmunology 384, 578213, 2023
32023
Recurrent sensory-motor neuropathy mimicking CIDP as predominant presentation of PDH deficiency
C Croci, M Cataldi, S Baratto, C Bruno, F Trucco, S Doccini, A Romano, ...
Neuropediatrics 54 (03), 211-216, 2023
12023
Multimodal approach in the pre‐surgical evaluation of focal epilepsy surgery candidates: how far are we from a non‐invasive ESI‐based “sourcectomy”?
G Nobile, A Consales, D Tortora, M Pacetti, F Gianno, D Arnaldi, ...
Epileptic Disorders 23 (4), 661-666, 2021
12021
Early onset inherited peripheral neuropathies: the experience of a specialized referral center for genetic diagnosis achievement.
A Geroldi, C Ponti, A Mammi, S Patrone, F Gotta, L Trevisan, F Sanguineri, ...
Pediatric Neurology, 2024
2024
Navigating the complexities of encephalocraniocutaneous lipomatosis: a case series and review
M Pavanello, L Piro, A Roggero, A Rossi, M Cataldi, G Piatelli
Child's Nervous System, 1-8, 2024
2024
A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers
A Geroldi, S Tozza, C Fiorillo, M Nolano, P Fossa, F Vitale, R Domi, ...
Journal of the Peripheral Nervous System 28 (4), 620-628, 2023
2023
N° 164–Reduced sleep spindle activity in Rett syndrome: A polysomnographic case-control study
M Cataldi, R Cordani, L Chiarella, M Veneruso, S Boeri, G Prato, ...
Clinical Neurophysiology 150, e124, 2023
2023
AN OVERVIEW OF CHILDHOOD NEUROPATHIES: A 24 YEARS'EXPERIENCE
A Geroldi, A Mammi, S Patrone, F Gotta, L Trevisan, C Ponti, F Sanguineri, ...
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM 27, S16-S17, 2022
2022
Magnetic resonance-guided laser interstitial thermal therapy for the treatment of hypothalamic hamartoma: report of 3 pediatric cases
E Cognolato, M Pacetti, D Tortora, A Rossi, G Prato, L Siri, M Cataldi, ...
EPILEPSIA 62, 200-201, 2021
2021
Musculoskeletal Features without Ataxia Associated with A Novel de novo Mutation in KCNA1 Impairing the Voltage Sensitivity of Kv1. 1 Channel. Biomedicines 2021, 9, 75
P Imbrici, A Accogli, R Blunck, C Altamura, M Iacomino, MC D’adamo, ...
s Note: MDPI stays neu-tral with regard to jurisdictional clai-ms in …, 2021
2021
Epilepsy Surgery: Early Versus Late Approach In A Pediatric Centre
C Croci, M Cataldi, T Giacomini, G Morana, A Consales, MM Mancardi, ...
EPILEPSIA 59, S207-S208, 2018
2018
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