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Stem Cell Research|March 29, 2024
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>ACamille Peron, Andrea Cavaliere, Chiara Fasano, et al.Journal of Neuroinflammation|February 26, 2013
An autoinflammatory neurological disease due to interleukin 6 hypersecretionEttore Salsano, Ambra Rizzo, Gloria Bedini, et al.Stem Cell Reports|July 30, 2021
The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCsFlavia Palombo, Camille Peron, Leonardo Caporali, et al.Neuroscience|August 11, 2019
Hyperexcitability in Cultured Cortical Neuron Networks from the G93A-SOD1 Amyotrophic Lateral Sclerosis Model Mouse and its Molecular CorrelatesStefania Marcuzzo, Benedetta Terragni, Silvia Bonanno, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 15, 2018
The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disordersAmbra Rizzo, Enrico Alfei, Federica Zibordi, et al.International Journal of Molecular Sciences|November 23, 2018
Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya SyndromeSciacca Francesca Luisa, Ambra Rizzo, Gloria Bedini, et al.International Journal of Molecular Sciences|December 22, 2019
Correction: Sciacca, F. L., et al. Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome. Int. J. Mol. Sci. 2018, 19, 3675Francesca Luisa Sciacca, Ambra Rizzo, Gloria Bedini, et al.Molecular Neurodegeneration|April 26, 2025
TDP-43 seeding activity in the olfactory mucosa of patients with amyotrophic lateral sclerosisMaria Vizziello, Ilaria Linda Dellarole, Arianna Ciullini, et al.Pageof 2