Maria G. Miano

Naples, Italy

Last Updated: 09/26/2026

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Found 19 publications

Sleep disruption and neuropsychiatric features in Angelman syndrome: insights into underlying neurobiology.

Sleep disruption and neuropsychiatric features in Angelman syndrome: insights into underlying neurobiology.

Journal: Sleep medicine

Published: April 27, 2026

The lysine methyltransferase KMT5a and p53 regulate the expression of the key autophagy adaptor p62/SQSTM1 in glioblastoma.

The lysine methyltransferase KMT5a and p53 regulate the expression of the key autophagy adaptor p62/SQSTM1 in glioblastoma.

Journal: Cell communication and signaling : CCS

Published: September 18, 2025

Microglial clearance, neuroprotection and cognitive recovery via a novel synthetic sulfolipid in Alzheimer's disease.

Microglial clearance, neuroprotection and cognitive recovery via a novel synthetic sulfolipid in Alzheimer's disease.

Journal: Journal of neuroinflammation

Published: August 18, 2025

RNA-based therapies for neurodevelopmental disorders: innovative tools for molecular correction.

RNA-based therapies for neurodevelopmental disorders: innovative tools for molecular correction.

Journal: Frontiers in molecular biosciences

Published: August 07, 2025

Cannabidiol attenuates epileptic phenotype and increases survival in a mouse model of developmental and epileptic encephalopathy type 1.

Cannabidiol attenuates epileptic phenotype and increases survival in a mouse model of developmental and epileptic encephalopathy type 1.

Journal: Epilepsia

Published: March 12, 2025

Suberoylanilide Hydroxamic Acid (SAHA) Is a Driver Molecule of Neuroplasticity: Implication for Neurological Diseases.

Suberoylanilide Hydroxamic Acid (SAHA) Is a Driver Molecule of Neuroplasticity: Implication for Neurological Diseases.

Journal: Biomolecules

Published: July 07, 2023

The Chromatin-Oxygen Sensor Gene KDM5C Associates with Novel Hypoxia-Related Signatures in Glioblastoma Multiforme.

The Chromatin-Oxygen Sensor Gene KDM5C Associates with Novel Hypoxia-Related Signatures in Glioblastoma Multiforme.

Journal: International journal of molecular sciences

Published: August 04, 2022

A Novel Splicing SCN2A Mutation in an Adolescent With Low-Functioning Autism, Acute Dystonic Movement Disorder, and Late-Onset Generalized Epilepsy.

A Novel Splicing SCN2A Mutation in an Adolescent With Low-Functioning Autism, Acute Dystonic Movement Disorder, and Late-Onset Generalized Epilepsy.

Journal: Pediatric neurology

Published: July 24, 2022

Expanding the genetics and phenotypic spectrum of Lysine-specific demethylase 5C (KDM5C): a report of 13 novel variants.

Expanding the genetics and phenotypic spectrum of Lysine-specific demethylase 5C (KDM5C): a report of 13 novel variants.

Journal: European journal of human genetics : EJHG

Published: April 08, 2022

Further Delineation of Duplications of ARX Locus Detected in Male Patients with Varying Degrees of Intellectual Disability.

Further Delineation of Duplications of ARX Locus Detected in Male Patients with Varying Degrees of Intellectual Disability.

Journal: International journal of molecular sciences

Published: February 17, 2022

Deregulation of microtubule organization and RNA metabolism in Arx models for lissencephaly and developmental epileptic encephalopathy.

Deregulation of microtubule organization and RNA metabolism in Arx models for lissencephaly and developmental epileptic encephalopathy.

Journal: Human molecular genetics

Published: October 30, 2021

Analysis of a Set of KDM5C Regulatory Genes Mutated in Neurodevelopmental Disorders Identifies Temporal Coexpression Brain Signatures.

Analysis of a Set of KDM5C Regulatory Genes Mutated in Neurodevelopmental Disorders Identifies Temporal Coexpression Brain Signatures.

Journal: Genes

Published: June 18, 2021

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Last Updated: 09/26/2026