Ivano Di Meo Unit of Medical Genetics and Neurogenetics Fondazione IRCCS Istituto Neurologico Carlo Besta Biography Publications Institution JoVE Articles Ivano Di Meo has not added a biography. If you are Ivano Di Meo and would like to personalize this page please email our Author Liaison for assistance. Publications Massive Iron Accumulation in PKAN-derived Neurons and Astrocytes: Light on the Human Pathological Phenotype Cell Death & Disease. 02, 2022 | Pubmed ID: 35217637 Novel Deep Intronic Mutation in PLA2G6 Causing Early-onset Parkinson's Disease with Brain Iron Accumulation Through Pseudo-exon Activation Neurogenetics. 10, 2021 | Pubmed ID: 34387792 The Relevance of Mitochondrial DNA Variants Fluctuation During Reprogramming and Neuronal Differentiation of Human IPSCs Stem Cell Reports. 08, 2021 | Pubmed ID: 34329598 Exploiting HiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives Frontiers in Neurology. 2021 | Pubmed ID: 34168607 Ethylmalonic Encephalopathy and Liver Transplantation: Long-term Outcome of the First Treated Patient Orphanet Journal of Rare Diseases. 05, 2021 | Pubmed ID: 34011365 A Novel Homozygous MSTO1 Mutation in Ashkenazi Jewish Siblings with Ataxia and Myopathy Journal of Human Genetics. Aug, 2021 | Pubmed ID: 33612823 Neuronal Ablation of CoA Synthase Causes Motor Deficits, Iron Dyshomeostasis, and Mitochondrial Dysfunctions in a CoPAN Mouse Model International Journal of Molecular Sciences. Dec, 2020 | Pubmed ID: 33352696 Homozygous Mutations in C1QBP As Cause of Progressive External Ophthalmoplegia (PEO) and Mitochondrial Myopathy with Multiple MtDNA Deletions Human Mutation. 10, 2020 | Pubmed ID: 32652806 An In Vitro Approach to Study Mitochondrial Dysfunction: A Cybrid Model Andrea Cavaliere*1, Silvia Marchet*1, Ivano Di Meo1, Valeria Tiranti1 1Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta JoVE 63452 Genetics
An In Vitro Approach to Study Mitochondrial Dysfunction: A Cybrid Model Andrea Cavaliere*1, Silvia Marchet*1, Ivano Di Meo1, Valeria Tiranti1 1Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta JoVE 63452 Genetics
