Search Results - "Miramondi, Federica"
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Identification of Region-Specific Cytoskeletal and Molecular Alterations in Astrocytes of Mecp2 Deficient Animals
Published in Frontiers in neuroscience (15-02-2022)“…Rett syndrome (RTT) is a neurodevelopmental disorder that represents the most common genetic cause of severe intellectual disability in females. Most patients…”
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Neural precursor cells rescue symptoms of Rett syndrome by activation of the Interferon γ pathway
Published in EMBO molecular medicine (20-09-2024)“…The beneficial effects of Neural Precursor Cell (NPC) transplantation in several neurological disorders are well established and they are generally mediated by…”
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Journal Article