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 | 21 | 2021 |
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 | 21 | 2020 |
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 | 13 | 2022 |
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 | 12 | 2019 |
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 | 11 | 2022 |
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 | 11 | 2021 |
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 | 5 | 2022 |
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 | 5 | 2022 |
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 | 5 | 2021 |
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 | 3 | 2023 |
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 | 1 | 2023 |
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 | 1 | 2021 |
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 |