Andrea Cavaliere
Milan, 20133, Italy
Last Updated: 09/26/2026
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Found 8 publications
Generation of iPSCs from identical twin, one affected by LHON and one unaffected, both carrying a combination of two mitochondrial variants: m.14484 T>C and m.10680G>A.
Journal: Stem cell research
Published: January 04, 2024
VCP-related myopathy: a case series and a review of literature.
Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
Published: January 11, 2023
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy.
Journal: Cell reports. Medicine
Published: January 05, 2023
An In Vitro Approach to Study Mitochondrial Dysfunction: A Cybrid Model.
Journal: Journal of visualized experiments : JoVE
Published: March 28, 2022
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy.
Journal: Cell reports
Published: June 17, 2021
Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives.
Journal: Frontiers in neurology
Published: January 02, 2021
Generation of two human iPSC lines, FINCBi002-A and FINCBi003-A, carrying heteroplasmic macrodeletion of mitochondrial DNA causing Pearson's syndrome.
Journal: Stem cell research
Published: October 20, 2020
Showing 1-8 of 8
Last Updated: 09/26/2026