Ida Manna

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 7

Top Topics

Traumatic Brain Injury

Multiple Sclerosis

Genome Wide Analysis

Mitochondrial Dna

Top Venues

International journal of molecular sciences

Amyotrophic lateral sclerosis & frontotemporal degeneration

This page only lists publications with an associated author ORCID identifier.

Publications

Ida Manna, Selene De Benedittis, Danilo Porro
Extracellular Vesicles in Multiple Sclerosis: Their Significance in the Development and Possible Applications as Therapeutic Agents and Biomarkers. Genes 15 (6) (2024)
Ida Manna, Selene De Benedittis, Danilo Porro
A Comprehensive Examination of the Role of Epigenetic Factors in Multiple Sclerosis. International journal of molecular sciences 25 (16) (2024)
Ida Manna, Selene De Benedittis, Danilo Porro
Extracellular Vesicles in Multiple Sclerosis: Their Significance in the Development and Possible Applications as Therapeutic Agents and Biomarkers. Genes 15 (6) (2024)
Ida Manna, Selene De Benedittis, Danilo Porro
A Comprehensive Examination of the Role of Epigenetic Factors in Multiple Sclerosis. International journal of molecular sciences 25 (16) (2024)
Ida Manna, Francesco Fortunato, Selene De Benedittis, Ilaria Sammarra, Gloria Bertoli, Angelo Labate, Antonio Gambardella
Non-Coding RNAs: New Biomarkers and Therapeutic Targets for Temporal Lobe Epilepsy. International journal of molecular sciences 23 (6) (2022)
Selene De Benedittis, Francesco Fortunato, Claudia Cava, Francesca Gallivanone, Enrico Iaccino, Maria Eugenia Caligiuri, Isabella Castiglioni, Gloria Bertoli, Ida Manna, Angelo Labate, Antonio Gambardella
Circulating microRNA: The Potential Novel Diagnostic Biomarkers to Predict Drug Resistance in Temporal Lobe Epilepsy, a Pilot Study. International journal of molecular sciences 22 (2) (2021)
Maurizio Morelli, Andrea Quattrone, Gennarina Arabia, Ida Manna, Antonio Gambardella, Aldo Quattrone
Hyper-religiosity and visual hallucinations in a patient with frontotemporal dementia carrying a double variant in GRN gene. Amyotrophic lateral sclerosis & frontotemporal degeneration (2021)