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Journal of Neurochemistry|February 4, 2009
Alterations of myelin-specific proteins and sphingolipids characterize the brains of acid sphingomyelinase-deficient mice, an animal model of Niemann-Pick disease type ABarbara Buccinnà, Marco Piccinini, Alessandro Prinetti, et al.International Journal of Molecular Sciences|November 9, 2024
GM1 Oligosaccharide Ameliorates Rett Syndrome Phenotypes In Vitro and In Vivo via Trk Receptor ActivationMaria Fazzari, Giulia Lunghi, Emma Veronica Carsana, et al.Biomedicines|April 29, 2025
Metabolic and Structural Consequences of GM3 Synthase Deficiency: Insights from an HEK293-T Knockout ModelElena Chiricozzi, Giulia Lunghi, Manuela Valsecchi, et al.Scientific Reports|December 20, 2019
Parkinson's disease recovery by GM1 oligosaccharide treatment in the B4galnt1+/- mouse modelElena Chiricozzi, Laura Mauri, Giulia Lunghi, et al.Nature Communications|June 7, 2014
iPSC-derived neurons from GBA1-associated Parkinson's disease patients show autophagic defects and impaired calcium homeostasisDavid C Schöndorf, Massimo Aureli, Fiona E McAllister, et al.Glycoconjugate Journal|December 15, 2023
GM1 structural requirements to mediate neuronal functionsMaria Fazzari, Giulia Lunghi, Erika Di Biase, et al.Pageof 3