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 माइटोकॉन्ड्रियल डिसफंक्शन का अध्ययन करने के लिए एक इन विट्रो दृष्टिकोण: एक साइब्रिड मॉडल 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
माइटोकॉन्ड्रियल डिसफंक्शन का अध्ययन करने के लिए एक इन विट्रो दृष्टिकोण: एक साइब्रिड मॉडल 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