Publications by authors named "Stefano Pro"

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Two Rare Cases of Bilateral Diaphragmatic Paralysis in Neonates.
Sara Ronci, Chiara Maddaloni, Stefano Caoci, Stefano Pro, Daniela Longo

Pediatr Rep· December 2025

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Segmental brainstem myoclonus in ADCK3-Related ataxia: A novel phenomenon?
Vito Luigi Colona, Giacomo Garone, Francesco Nicita, Lorena Travaglini, Stefano Pro

Parkinsonism Relat Disord· January 2025

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Isolated Intracranial Hypertensions as Onset of Myelin Oligodendrocyte Glycoprotein Antibody Disease.
Laura Papetti, Giulia Moltoni, Daniela Longo, Gabriele Monte, Francesco Dellepiane, Stefano Pro

J Clin Med· July 2024

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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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Spectrum of -Related Cockayne Syndrome (Type B): From Mild to Severe Forms.
Jacopo Sartorelli, Lorena Travaglini, Marina Macchiaiolo, Giacomo Garone, Michaela Veronika Gonfiantini, Stefano Pro

Genes (Basel)· April 2024

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A New Case of Autosomal-Dominant -Related Disorder: Widening Genotypic and Phenotypic .
Vito Luigi Colona, Enrico Bertini, Maria Cristina Digilio, Adele D'Amico, Antonio Novelli, Stefano Pro

Brain Sci· November 2023

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Vocal Cord Paralysis and Feeding Difficulties as Early Diagnostic Clues of Congenital Myasthenic Syndrome with Neonatal Onset: A Case Report and Review of Literature.
Domenico Umberto De Rose, Sara Ronci, Stefano Caoci, Chiara Maddaloni, Daria Diodato, Stefano Pro

J Pers Med· May 2023

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Neurodevelopmental and genetic findings in neonates with intracranial arteriovenous shunts: A case series.
Francesca Campi, Domenico Umberto De Rose, Flaminia Pugnaloni, Sara Ronci, Monica Calì, Stefano Pro

Front Pediatr· March 2023

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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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"Atypical" Krabbe disease in two siblings harboring biallelic GALC mutations including a deep intronic variant.
Francesco Nicita, Fabrizia Stregapede, Federica Deodato, Simone Pizzi, Simone Martinelli, Stefano Pro

Eur J Hum Genet· August 2022

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Case report: A pediatric case of Bickerstaff brainstem encephalitis after COVID-19 vaccination and Mycoplasma pneumoniae infection: Looking for the culprit.
Gabriele Monte, Stefano Pro, Fabiana Ursitti, Michela Ada Noris Ferilli, Romina Moavero

Front Immunol· August 2022

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Novel Pathogenic Variants Featuring Unusual Phenotype of Complex Movement Disorder With Thin Corpus Callosum: A Case Report.
Francesco Nicita, Lorena Travaglini, Francesco Bombelli, Michele Tosi, Stefano Pro

Neurol Genet· April 2022

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Short and Long-Term Toxicity in Pediatric Cancer Treatment: Central Nervous System Damage.
Iside Alessi, Anna Maria Caroleo, Luca de Palma, Angela Mastronuzzi, Stefano Pro

Cancers (Basel)· March 2022

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High Intellectual Potential and High Functioning Autism: Clinical and Neurophysiological Features in a Pediatric Sample.
Assia Riccioni, Stefano Pro, Lorena Di Criscio, Monica Terribili, Martina Siracusano

Brain Sci· December 2021

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Age-related sensory neuropathy in patients with spinal muscular atrophy type 1.
Stefano Pro, Alberto Eugenio Tozzi, Adele D'Amico, Michela Catteruccia, Claudio Cherchi

Muscle Nerve· November 2021

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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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Peripheral Nervous System Involvement in Non-Primary Pediatric Cancer: From Neurotoxicity to Possible Etiologies.
Stefano Pro, Luciana Vinti, Alessandra Boni, Angela Mastronuzzi, Martina Scilipoti

J Clin Med· July 2021

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Acute strabismus in neurological emergencies of childhood: A retrospective, single-centre study.
Giacomo Garone, Valentina Ferro, Marta Barbato, Nicola Vanacore, Laura Papini, Stefano Pro

Eur J Paediatr Neurol· May 2021

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Event-Related Potentials in ADHD Associated With Tuberous Sclerosis Complex: A Possible Biomarker of Symptoms Severity?
Romina Moavero, Sara Marciano, Stefano Pro, Donata De Stefano, Federico Vigevano

Front Neurol· July 2020

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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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Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutation.
Fabrizia Stregapede, Lorena Travaglini, Adriana P Rebelo, Vivian Pedigone Cintra, Emanuele Bellacchio, Stefano Pro

Clin Genet· March 2020

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Visual pathways evaluation in Kearns Sayre syndrome: a diffusion tensor imaging study.
Maria Camilla Rossi-Espagnet, Martina Lucignani, Luca Pasquini, Antonio Napolitano, Stefano Pro

Neuroradiology· February 2020

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Reply to: Viability of diffusion tensor imaging for assessing retrochiasmatic involvement in Kearns-Sayre syndrome remains elusive.
Maria Camilla Rossi-Espagnet, Stefano Pro, Diego Martinelli, Daria Diodato, Antonio Napolitano

Neuroradiology· February 2020

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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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A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorder.
Federica Graziola, Fabrizia Stregapede, Lorena Travaglini, Giacomo Garone, Margherita Verardo, Stefano Pro

Parkinsonism Relat Disord· April 2019

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