Ester Gallardo-Lopez
Madrid, MD, Spain
Last Updated: 09/26/2026
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Found 40 publications
Effects of a Mitochondrial Genetic Variant on Sevoflurane Hypersensitivity.
Journal: Anesthesiology
Published: May 12, 2026
Effects of Tributyltin Chloride on Human Neuronal Differentiation and Mice Brain Development.
Journal: Environmental toxicology
Published: May 08, 2025
Identification and characterization of a new pathologic mutation in a large Leber hereditary optic neuropathy pedigree.
Journal: Orphanet journal of rare diseases
Published: October 29, 2023
Pathological Features in Paediatric Patients with TK2 Deficiency.
Journal: International journal of molecular sciences
Published: August 12, 2022
Is population frequency a useful criterion to assign pathogenicity to newly described mitochondrial DNA variants?
Journal: Orphanet journal of rare diseases
Published: March 10, 2022
Multicentric Standardization of Protocols for the Diagnosis of Human Mitochondrial Respiratory Chain Defects.
Journal: Antioxidants (Basel, Switzerland)
Published: February 02, 2022
Development and characterization of cell models harbouring mtDNA deletions for in vitro study of Pearson syndrome.
Journal: Disease models & mechanisms
Published: April 28, 2021
Genetic aspects of the oxidative phosphorylation dysfunction in dilated cardiomyopathy.
Journal: Mutation research. Reviews in mutation research
Published: March 22, 2020
Oxidative Phosphorylation Dysfunction Modifies the Cell Secretome.
Journal: International journal of molecular sciences
Published: March 18, 2020
Mitochondrial DNA pathogenic mutations in multiple symmetric lipomatosis.
Journal: Clinical genetics
Published: November 25, 2019
Ketogenic treatment reduces the percentage of a LHON heteroplasmic mutation and increases mtDNA amount of a LHON homoplasmic mutation.
Journal: Orphanet journal of rare diseases
Published: January 15, 2019
Last Updated: 09/26/2026