Search Results - "Mottolese, Nicola"

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    Inhibition of microglia overactivation restores neuronal survival in a mouse model of CDKL5 deficiency disorder by Galvani, Giuseppe, Mottolese, Nicola, Gennaccaro, Laura, Loi, Manuela, Medici, Giorgio, Tassinari, Marianna, Fuchs, Claudia, Ciani, Elisabetta, Trazzi, Stefania

    Published in Journal of neuroinflammation (08-07-2021)
    “…CDKL5 deficiency disorder (CDD), a severe neurodevelopmental disorder characterized by early onset epilepsy, intellectual disability, and autistic features, is…”
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    Journal Article
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    Early-onset brain alterations during postnatal development in a mouse model of CDKL5 deficiency disorder by Tassinari, Marianna, Uguagliati, Beatrice, Trazzi, Stefania, Cerchier, Camilla Bruna, Cavina, Ottavia Vera, Mottolese, Nicola, Loi, Manuela, Candini, Giulia, Medici, Giorgio, Ciani, Elisabetta

    Published in Neurobiology of disease (15-06-2023)
    “…Mutations in the CDKL5 gene are the cause of CDKL5 deficiency disorder (CDD), a rare and severe neurodevelopmental condition characterized by early-onset…”
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    Voluntary Running Improves Behavioral and Structural Abnormalities in a Mouse Model of CDKL5 Deficiency Disorder by Mottolese, Nicola, Uguagliati, Beatrice, Tassinari, Marianna, Cerchier, Camilla Bruna, Loi, Manuela, Candini, Giulia, Rimondini, Roberto, Medici, Giorgio, Trazzi, Stefania, Ciani, Elisabetta

    Published in Biomolecules (Basel, Switzerland) (01-09-2023)
    “…Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a rare neurodevelopmental disease caused by mutations in the X-linked CDKL5 gene. CDD is…”
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    Journal Article
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    Autistic‐relevant behavioral phenotypes of a mouse model of cyclin‐dependent kinase‐like 5 deficiency disorder by Mottolese, Nicola, Coiffard, Oceane, Ferraguto, Celeste, Manolis, Athanasios, Ciani, Elisabetta, Pietropaolo, Susanna

    Published in Autism research (01-09-2024)
    “…Cyclin‐dependent kinase‐like 5 (CDKL5) deficiency disorder (CDD) is a neurodevelopmental disease caused by mutations in the X‐linked CDKL5 gene and…”
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    Journal Article
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