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

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Research Output

Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study

for the FTD Prevention Initiative, Moore, K. M., Nicholas, J., Grossman, M., McMillan, C. T., Irwin, D. J., Massimo, L., Van Deerlin, V. M., Warren, J. D., Fox, N. C., Rossor, M. N., Mead, S., Bocchetta, M., Boeve, B. F., Knopman, D. S., Graff-Radford, N. R., Forsberg, L. K., Rademakers, R., Wszolek, Z. K., van Swieten, J. C. & 31 others, Jiskoot, L. C., Meeter, L. H., Dopper, E. GP., Papma, J. M., Snowden, J. S., Saxon, J., Jones, M., Pickering-Brown, S., Le Ber, I., Camuzat, A., Brice, A., Caroppo, P., Ghidoni, R., Pievani, M., Benussi, L., Binetti, G., Dickerson, B. C., Lucente, D., Krivensky, S., Graff, C., Öijerstedt, L., Borroni, B., Galimberti, D., Scarpini, E., Fumagalli, G. G., Sorbi, S., Frisoni, G., Mega, A., Fostinelli, S., Arighi, A. & Fenoglio, C., Feb 2020, In : The Lancet Neurology. 19, 2, p. 145-156 12 p.

Research output: Contribution to journalArticle

Open Access
  • 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
  • CSF β-amyloid predicts early cerebellar atrophy and is associated with a poor prognosis in multiple sclerosis

    Pietroboni, A. M., Schiano di Cola, F., Colombi, A., Carandini, T., Fenoglio, C., Ghezzi, L., De Riz, M. A., Triulzi, F., Scarpini, E., Padovani, A. & Galimberti, D., Jan 2020, In : Multiple Sclerosis and Related Disorders. 37, 101462.

    Research output: Contribution to journalArticle

  • Erratum: Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk (Cell (2019) 178(1) (262), (S0092867419306798), (10.1016/j.cell.2019.06.016))

    International Multiple Sclerosis Genetics Consortium, Jan 23 2020, In : Cell. 180, 2, 1 p.

    Research output: Contribution to journalComment/debate

    Open Access