Publications by authors named "Maria Lieto"

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ACT-ON-DIP: Study Protocol of a Randomized Controlled Trial of a Home-Based ACTion Observation Tele-RehabilitatioN for Upper Limb in Children with DIPlegic Cerebral Palsy.
Elena Beani, Elisa Matteucci, Elisa Sicola, Giada Martini, Maria Chiara Di Lieto

Children (Basel)· September 2025

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Impact of social participation, motor, and cognitive functioning on quality of life in children with Cerebral Palsy.
Maria Chiara Di Lieto, Elisa Matteucci, Alice Martinelli, Elena Beani, Valentina Menici

Res Dev Disabil· June 2025

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The wide world of technological telerehabilitation for pediatric neurologic and neurodevelopmental disorders - a systematic review.
Benedetta Del Lucchese, Stefano Parravicini, Silvia Filogna, Gloria Mangani, Elena Beani, Maria Chiara Di Lieto

Front Public Health· April 2025

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SCAR32: Functional characterization and expansion of the clinical-genetic spectrum.
Valentina Naef, Maria Lieto, Sara Satolli, Rosa De Micco, Martina Troisi

Ann Clin Transl Neurol· July 2024

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Far Transfer Effects of Trainings on Executive Functions in Neurodevelopmental Disorders: A Systematic Review and Metanalysis.
Clara Bombonato, Benedetta Del Lucchese, Costanza Ruffini, Maria Chiara Di Lieto, Paola Brovedani

Neuropsychol Rev· March 2024

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Specific Learning Disabilities and Emotional-Behavioral Difficulties: Phenotypes and Role of the Cognitive Profile.
Paola Cristofani, Maria Chiara Di Lieto, Claudia Casalini, Chiara Pecini, Matteo Baroncini

J Clin Med· February 2023

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Complex neurodevelopmental disorder in a preterm child with unilateral cerebellar hemorrhage.
Eleonora Bonaventura, Giulia Purpura, Rosa Pasquariello, Sara Da Prato, Maria Chiara Di Lieto

Appl Neuropsychol Child· October 2022

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A case of febrile infection-related epilepsy syndrome (FIRES) in young adult: still a diagnostic and therapeutic challenge.
Roberto Acampora, Pablo Quiroga Subirana, Luana Durante, Rossella Tonziello, Giuseppina Aversano, Maria Lieto

Neurol Sci· July 2022

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Executive Functions and Rapid Automatized Naming: A New Tele-Rehabilitation Approach in Children with Language and Learning Disorders.
Agnese Capodieci, Marco Romano, Emanuela Castro, Maria Chiara Di Lieto, Silvia Bonetti

Children (Basel)· June 2022

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Recurrent convulsive syncope misdiagnosed as seizures due to a diaphragmatic hernia.
Roberto Acampora, Gianpaolo Marte, Rossana Scala, Maria Lieto, Pietro Maida

Neurol Sci· November 2021

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Variants in cause progressive myoclonus epilepsy and developmental and epileptic encephalopathy.
Laura C Bott, Mitra Forouhan, Maria Lieto, Ambre J Sala, Ruth Ellerington

Brain Commun· October 2021

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Gene therapy with AR isoform 2 rescues spinal and bulbar muscular atrophy phenotype by modulating AR transcriptional activity.
Wooi F Lim, Mitra Forouhan, Thomas C Roberts, Jesse Dabney, Ruth Ellerington, Maria Lieto

Sci Adv· August 2021

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NGS in Hereditary Ataxia: When Rare Becomes Frequent.
Daniele Galatolo, Giovanna De Michele, Gabriella Silvestri, Vincenzo Leuzzi, Carlo Casali, Maria Lieto

Int J Mol Sci· August 2021

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Dialogic Reading to Empower Executive Functions in Preschoolers.
Costanza Ruffini, Silvia Spoglianti, Clara Bombonato, Silvia Bonetti, Maria Chiara Di Lieto

Children (Basel)· May 2021

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Adaptive Working Memory Training Can Improve Executive Functioning and Visuo-Spatial Skills in Children With Pre-term Spastic Diplegia.
Maria Chiara Di Lieto, Chiara Pecini, Paola Brovedani, Giuseppina Sgandurra, Marta Dell'Omo

Front Neurol· January 2021

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Application of the p9NORM correction method to timed neuropsychological tests in Parkinson's disease and multiple system atrophy.
Teresa Costabile, Chiara Pane, Luisa Aurisicchio, Adriana Salvati, Maria Lieto

Neurol Sci· December 2020

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New Mutations in Two Siblings With Tremor, Downbeat Nystagmus, and Primary Amenorrhea: A Benign Phenotype Without Leukoencephalopathy.
Giovanna De Michele, Daniele Galatolo, Maria Lieto, Luigi Maione, Sirio Cocozza

Mov Disord Clin Pract· August 2020

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Bi-allelic mutations in HARS1 severely impair histidyl-tRNA synthetase expression and enzymatic activity causing a novel multisystem ataxic syndrome.
Daniele Galatolo, Molly E Kuo, Patrick Mullen, Rebecca Meyer-Schuman, Stefano Doccini, Maria Lieto

Hum Mutat· July 2020

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Ataxia-myoclonus syndrome due to a novel homozygous ATP13A2 mutation.
Giovanna De Michele, Daniele Galatolo, Maria Lieto, Tommasina Fico, Francesco Saccà

Parkinsonism Relat Disord· July 2020

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Cerebellum and cognition in Friedreich ataxia: a voxel-based morphometry and volumetric MRI study.
Sirio Cocozza, Teresa Costabile, Giuseppe Pontillo, Maria Lieto, Camilla Russo

J Neurol· February 2020

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Empowering Executive Functions in 5- and 6-Year-Old Typically Developing Children Through Educational Robotics: An RCT Study.
Maria Chiara Di Lieto, Chiara Pecini, Emanuela Castro, Emanuela Inguaggiato, Francesca Cecchi

Front Psychol· February 2020

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Improving Executive Functions at School in Children With Special Needs by Educational Robotics.
Maria Chiara Di Lieto, Emanuela Castro, Chiara Pecini, Emanuela Inguaggiato, Francesca Cecchi

Front Psychol· January 2020

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Dystonia-Ataxia with early handwriting deterioration in COQ8A mutation carriers: A case series and literature review.
Serena Galosi, Emanuele Barca, Rosalba Carrozzo, Tommaso Schirinzi, Catarina Maria Quinzii, Maria Lieto

Parkinsonism Relat Disord· November 2019

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Overt Hypogonadism May Not Be a Sentinel Sign of RING Finger Protein 216: Two Novel Mutations Associated with Ataxia, Chorea, and Fertility.
Maria Lieto, Daniele Galatolo, Alessandro Roca, Sirio Cocozza, Giuseppe Pontillo

Mov Disord Clin Pract· November 2019

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Longitudinal study of a cohort of MSA-C patients in South Italy: survival and clinical features.
Maria Lieto, Alessandro Roca, Dario Bruzzese, Antonella Antenora, Girolamo Alfieri

Neurol Sci· October 2019

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