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Fingerprint Dive into the research topics where Giorgio Giaccone is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Research Output

Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (Acta Neuropathologica, (2019), 138, 2, (237-250), 10.1007/s00401-019-02026-8)

EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementia), Netherlands Brain Bank (NBB), The GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group & DESGESCO (Dementia Genetics Spanish Consortium), Jan 1 2020, (Accepted/In press) In : Acta Neuropathologica.

Research output: Contribution to journalComment/debate

Open Access
  • Discovering the Italian phenotype of cerebral amyloid angiopathy (CAA): the SENECA project

    on behalf of SENECA project, Jan 1 2020, (Accepted/In press) In : Neurological Sciences.

    Research output: Contribution to journalArticle

  • Understanding the pathophysiology of cerebral amyloid angiopathy

    Gatti, L., Tinelli, F., Scelzo, E., Arioli, F., Di Fede, G., Obici, L., Pantoni, L., Giaccone, G., Caroppo, P., Parati, E. A. & Bersano, A., May 2 2020, In : International Journal of Molecular Sciences. 21, 10, 3435.

    Research output: Contribution to journalReview article

    Open Access
  • An atypical presentation of diffuse midline pontine glioma in a middle age patient: Case report

    Floro, S., Belvedere, D., Rosci, C., Secchi, M., Casellato, C., Oggioni, G., Gambini, C., Campiglio, L., Zardoni, M., Altavilla, R., Bianchi, F., D'Arrigo, A., Bartesaghi, F., Egidi, M., Uggetti, C., Giaccone, G., Marucci, G., Mastronuzzi, A., Vinci, M. & Priori, A., Sep 20 2019, In : Journal of Clinical Neuroscience.

    Research output: Contribution to journalArticle

  • Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene

    Di Fede, G., Catania, M., Atzori, C., Moda, F., Pasquali, C., Indaco, A., Grisoli, M., Zuffi, M., Guaita, M. C., Testi, R., Taraglio, S., Sessa, M., Gusmaroli, G., Spinelli, M., Salzano, G., Legname, G., Tarletti, R., Godi, L., Pocchiari, M., Tagliavini, F. & 2 others, Imperiale, D. & Giaccone, G., Jan 3 2019, In : Acta neuropathologica communications. 7, 1, 1.

    Research output: Contribution to journalArticle