Maria Lieto

Naples, Italy

Last Updated: 09/26/2026

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Found 31 publications

Perampanel effects on seizures and sleep quality in people with epilepsy: A prospective multicenter study.

Perampanel effects on seizures and sleep quality in people with epilepsy: A prospective multicenter study.

Journal: Epilepsy & behavior : E&B
Published: August 13, 2025

SCAR32: Functional characterization and expansion of the clinical-genetic spectrum.

SCAR32: Functional characterization and expansion of the clinical-genetic spectrum.

Journal: Annals of clinical and translational neurology
Published: March 25, 2024

Delayed onset Bickerstaff brainstem encephalitis overlapping Miller-Fisher Syndrome during SARS-CoV-2 infection.

Delayed onset Bickerstaff brainstem encephalitis overlapping Miller-Fisher Syndrome during SARS-CoV-2 infection.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: August 30, 2023

A case of febrile infection-related epilepsy syndrome (FIRES) in young adult: still a diagnostic and therapeutic challenge.

A case of febrile infection-related epilepsy syndrome (FIRES) in young adult: still a diagnostic and therapeutic challenge.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: February 17, 2022

Variants in ATP6V0A1 cause progressive myoclonus epilepsy and developmental and epileptic encephalopathy.

Variants in ATP6V0A1 cause progressive myoclonus epilepsy and developmental and epileptic encephalopathy.

Journal: Brain communications
Published: July 02, 2021

NGS in Hereditary Ataxia: When Rare Becomes Frequent.

NGS in Hereditary Ataxia: When Rare Becomes Frequent.

Journal: International journal of molecular sciences
Published: June 23, 2021

Recurrent convulsive syncope misdiagnosed as seizures due to a diaphragmatic hernia.

Recurrent convulsive syncope misdiagnosed as seizures due to a diaphragmatic hernia.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: May 05, 2021

Gene therapy with AR isoform 2 rescues spinal and bulbar muscular atrophy phenotype by modulating AR transcriptional activity.

Gene therapy with AR isoform 2 rescues spinal and bulbar muscular atrophy phenotype by modulating AR transcriptional activity.

Journal: Science advances
Published: March 25, 2021

Ataxia-myoclonus syndrome due to a novel homozygous ATP13A2 mutation.

Ataxia-myoclonus syndrome due to a novel homozygous ATP13A2 mutation.

Journal: Parkinsonism & related disorders
Published: April 27, 2020

New AARS2 Mutations in Two Siblings With Tremor, Downbeat Nystagmus, and Primary Amenorrhea: A Benign Phenotype Without Leukoencephalopathy.

New AARS2 Mutations in Two Siblings With Tremor, Downbeat Nystagmus, and Primary Amenorrhea: A Benign Phenotype Without Leukoencephalopathy.

Journal: Movement disorders clinical practice
Published: March 09, 2020

Application of the p9NORM correction method to timed neuropsychological tests in Parkinson's disease and multiple system atrophy.

Application of the p9NORM correction method to timed neuropsychological tests in Parkinson's disease and multiple system atrophy.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: February 17, 2020

Bi-allelic mutations in HARS1 severely impair histidyl-tRNA synthetase expression and enzymatic activity causing a novel multisystem ataxic syndrome.

Bi-allelic mutations in HARS1 severely impair histidyl-tRNA synthetase expression and enzymatic activity causing a novel multisystem ataxic syndrome.

Journal: Human mutation
Published: January 20, 2020
Showing 1-12 of 31

Last Updated: 09/26/2026