Alessandra Maresca

Via Altura 3
Bologna, 40139, Italy

Last Updated: 09/26/2026

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Found 67 publications

Lipidomics Based on HILIC-ESI-HRMS Reveal Subtle Changes in the Mitochondrial Phospholipidome of Mouse Embryonic Fibroblasts Expressing Pathogenic Variants of Human OPA1 Protein.

Lipidomics Based on HILIC-ESI-HRMS Reveal Subtle Changes in the Mitochondrial Phospholipidome of Mouse Embryonic Fibroblasts Expressing Pathogenic Variants of Human OPA1 Protein.

Journal: Molecules (Basel, Switzerland)

Published: June 09, 2026

Mutations Causative of CPEO Differentially Engage Innate Immunity Sensors.

Mutations Causative of CPEO Differentially Engage Innate Immunity Sensors.

Journal: bioRxiv : the preprint server for biology

Published: June 05, 2026

Biomarking MELAS with neurofilament light chain and circulating cell free mitochondrial DNA.

Biomarking MELAS with neurofilament light chain and circulating cell free mitochondrial DNA.

Journal: Molecular genetics and metabolism

Published: October 03, 2025

Late-onset Leber's hereditary optic neuropathy and antiandrogens for prostate cancer: is there a causative link?

Late-onset Leber's hereditary optic neuropathy and antiandrogens for prostate cancer: is there a causative link?

Journal: Frontiers in neurology

Published: April 23, 2025

Pluripotent stem-cell-based screening uncovers sildenafil as a mitochondrial disease therapy.

Pluripotent stem-cell-based screening uncovers sildenafil as a mitochondrial disease therapy.

Journal: Cell

Published: April 14, 2025

Elevated circulating cell-free mitochondrial DNA level in cerebrospinal fluid of narcolepsy type 1.

Elevated circulating cell-free mitochondrial DNA level in cerebrospinal fluid of narcolepsy type 1.

Journal: Brain communications

Published: December 18, 2024

Progressive encephalopathy in m.3243A > G/MT-TL1 mutation carriers: a quantitative EEG analysis.

Progressive encephalopathy in m.3243A > G/MT-TL1 mutation carriers: a quantitative EEG analysis.

Journal: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology

Published: August 21, 2024

Lipidomics reveals the reshaping of the mitochondrial phospholipid profile in cells lacking OPA1 and mitofusins.

Lipidomics reveals the reshaping of the mitochondrial phospholipid profile in cells lacking OPA1 and mitofusins.

Journal: Journal of lipid research

Published: April 01, 2024

Glutamine Supplementation as a Novel Metabolic Therapeutic Strategy for LIG3-Dependent Chronic Intestinal Pseudo-Obstruction.

Glutamine Supplementation as a Novel Metabolic Therapeutic Strategy for LIG3-Dependent Chronic Intestinal Pseudo-Obstruction.

Journal: Gastroenterology

Published: February 15, 2024

Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum Disorder.

Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum Disorder.

Journal: Research square

Published: November 14, 2023

Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates.

Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates.

Journal: NPJ genomic medicine

Published: October 20, 2023

Recessive MECR pathogenic variants cause an LHON-like optic neuropathy.

Recessive MECR pathogenic variants cause an LHON-like optic neuropathy.

Journal: Journal of medical genetics

Published: April 17, 2023

Showing 1-12 of 67

Last Updated: 09/26/2026