Publications by authors named "Matteo DI Capua"

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Brain auditory evoked potentials in pediatric Intensive Care Unit: diagnostic role on encephalopathy and central respiratory failure on infants.
Emanuele Rossetti, Stefano Pro, Sergio Picardo, Daniela Longo, Matteo DI Capua

Minerva Pediatr (Torino)· April 2024

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Early electroencephalogram and somatosensory evoked potentials as prognostic bedside tools in the pediatric cardiac intensive care.
Francesca G Iodice, Stefano Pro, Claudia Iacoella, Luca DI Chiara, Matteo DI Capua

Minerva Pediatr (Torino)· December 2022

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Neonatal Cerebral Venous Thrombosis following Maternal SARS-CoV-2 Infection in Pregnancy.
Francesca Campi, Daniela Longo, Iliana Bersani, Immacolata Savarese, Giulia Lucignani, Matteo Di Capua

Neonatology· March 2022

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Childhood-Onset Multifocal Motor Neuropathy with IgM Antibodies to Gangliosides GM1: A Case Report with Poor Outcome.
Stefano Pro, Fabiana Ursitti, Gian Luca Pruneddu, Matteo Di Capua, Massimiliano Valeriani

Neuropediatrics· October 2021

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Consensus protocol for EEG and amplitude-integrated EEG assessment and monitoring in neonates.
Robertino Dilena, Federico Raviglione, Gaetano Cantalupo, Duccio M Cordelli, Paola De Liso, Matteo Di Capua

Clin Neurophysiol· April 2021

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A reappraisal of the value of video-EEG recording in the emergency department.
Umberto Raucci, Stefano Pro, Matteo Di Capua, Giovanni Di Nardo, Maria Pia Villa

Expert Rev Neurother· May 2020

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Influence of etiology on treatment choices for neonatal seizures: A survey among pediatric neurologists.
Robertino Dilena, Paola De Liso, Matteo Di Capua, Dario Consonni, Giuseppe Capovilla

Brain Dev· August 2019

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Corticospinal tract damage in HHH syndrome: a metabolic cause of hereditary spastic paraplegia.
Giorgia Olivieri, Stefano Pro, Daria Diodato, Matteo Di Capua, Daniela Longo

Orphanet J Rare Dis· August 2019

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Axonal peripheral neuropathy in propionic acidemia: A severe side effect of long-term metronidazole therapy.
Daria Diodato, Giorgia Olivieri, Sefano Pro, Daniela Maiorani, Diego Martinelli, Matteo Di Capua

Neurology· September 2018

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Bilateral loss of cortical SEPs predict severe MRI lesions in neonatal hypoxic ischemic encephalopathy treated with hypothermia.
Agnese Suppiej, Ambra Cappellari, Giacomo Talenti, Elisa Cainelli, Matteo Di Capua

Clin Neurophysiol· January 2018

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Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia.
Lorena Travaglini, Marta Nardella, Emanuele Bellacchio, Adele D'Amico, Alessandro Capuano, Matteo Di Capua

Eur J Paediatr Neurol· May 2017

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Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain Perception.
Deborah Chiabrando, Marco Castori, Maja di Rocco, Martin Ungelenk, Sebastian Gießelmann, Matteo Di Capua

PLoS Genet· December 2016

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A Novel Mutation in RPL10 (Ribosomal Protein L10) Causes X-Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo-Epiphyseal Dysplasia.
Ginevra Zanni, Vera M Kalscheuer, Andreas Friedrich, Sabina Barresi, Paolo Alfieri, Matteo Di Capua

Hum Mutat· December 2015

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Longitudinal myelitis in systemic lupus erythematosus: a paediatric case.
Andrea Campana, Paola Sabrina Buonuomo, Antonella Insalaco, Claudia Bracaglia, Matteo Di Capua

Rheumatol Int· August 2012

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Ring 21 chromosome presenting with epilepsy and intellectual disability: clinical report and review of the literature.
Nicola Specchio, Antonio Carotenuto, Marina Trivisano, Simona Cappelletti, Cristina Digilio, Matteo Di Capua

Am J Med Genet A· April 2011

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Subdural fluid collections in patients with infantile neuronal ceroid lipofuscinosis.
Sondra W Levin, Eva H Baker, Andrea Gropman, Zenaide Quezado, Ning Miao, Matteo Di Capua

Arch Neurol· December 2009

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A Multicentre Database for Normative Brainstem Auditory Evoked Potentials (BAEPs) in Children: Methodology for Data Collection and Evaluation.
Vidmer Scaioli, Mario Brinciotti, Matteo Di Capua, Silvia Lori, Augusta Janes

Open Neurol J· October 2009

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Intravenous levetiracetam terminates refractory status epilepticus in two patients with migrating partial seizures in infancy.
Maria Roberta Cilio, Roberto Bianchi, Martina Balestri, Alfredo Onofri, Simona Giovannini, Matteo Di Capua

Epilepsy Res· September 2009

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Biochemical and molecular characterization of 18 patients with pyridoxine-dependent epilepsy and mutations of the antiquitin (ALDH7A1) gene.
Barbara Plecko, Karl Paul, Eduard Paschke, Sylvia Stoeckler-Ipsiroglu, Eduard Struys, Matteo di Capua

Hum Mutat· January 2007

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Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene.
Eleonore Eymard-Pierre, Gaetan Lesca, Sandra Dollet, Filippo Maria Santorelli, Matteo di Capua

Am J Hum Genet· September 2002

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