Border-independent multi-functional, multi-hazard exposure modelling in Alpine regions
Pittore, M., Campalani, P., Renner, K., Plörer, M., Tagliavini, F.
Published in Natural hazards (Dordrecht) (01.11.2023)
Published in Natural hazards (Dordrecht) (01.11.2023)
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Differential overexpression of SERPINA3 in human prion diseases
Vanni, S., Moda, F., Zattoni, M., Bistaffa, E., De Cecco, E., Rossi, M., Giaccone, G., Tagliavini, F., Haïk, S., Deslys, J. P., Zanusso, G., Ironside, J. W., Ferrer, I., Kovacs, G. G., Legname, G.
Published in Scientific reports (15.11.2017)
Published in Scientific reports (15.11.2017)
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Italian consensus recommendations for a biomarker‐based aetiological diagnosis in mild cognitive impairment patients
Boccardi, M., Nicolosi, V., Festari, C., Bianchetti, A., Cappa, S., Chiasserini, D., Falini, A., Guerra, U.P., Nobili, F., Padovani, A., Sancesario, G., Morbelli, S., Parnetti, L., Tiraboschi, P., Muscio, C., Perani, D., Pizzini, F.B., Beltramello, A., Salvini Porro, G., Ciaccio, M., Schillaci, O., Trabucchi, M., Tagliavini, F., Frisoni, G.B.
Published in European journal of neurology (01.03.2020)
Published in European journal of neurology (01.03.2020)
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Journal Article
In Situ Tissue Labeling of Cerebral Amyloid Using HIV-Related Tat Peptide
Maderna, E., Colombo, L., Cagnotto, A., Di Fede, G., Indaco, A., Tagliavini, F., Salmona, M., Giaccone, G.
Published in Molecular neurobiology (01.08.2018)
Published in Molecular neurobiology (01.08.2018)
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Journal Article
Stereotypic behaviors in degenerative dementias
Prioni, S., Fetoni, V., Barocco, F., Redaelli, V., Falcone, C., Soliveri, P., Tagliavini, F., Scaglioni, A., Caffarra, P., Concari, L., Gardini, S., Girotti, F.
Published in Journal of neurology (01.11.2012)
Published in Journal of neurology (01.11.2012)
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Journal Article
Multiple forms of PKR present in the nuclei of acute leukemia cells represent an active kinase that is responsive to stress
Blalock, W L, Bavelloni, A, Piazzi, M, Tagliavini, F, Faenza, I, Martelli, A M, Follo, M Y, Cocco, L
Published in Leukemia (01.02.2011)
Published in Leukemia (01.02.2011)
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Severe microcephaly with polynodular heterotopia: a high-field MRI and neuropathological case study
Minati, L., Giaccone, G., D'Incerti, L., Zucca, I., Spreafico, R., Tagliavini, F., Pilleri, G.
Published in European journal of neurology (01.06.2013)
Published in European journal of neurology (01.06.2013)
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Effectiveness of anthracycline against experimental prion disease in Syrian hamsters
Tagliavini, F. (Istituto Nazionale Neurologico Carlo Besta, Milano, Italy.), McArthur, R.A, Canciani, B, Giaccone, G, Porro, M, Bugiani, M, Lievens, P.M.J, Bugiani, O, Peri, E, Dall'Ara, P
Published in Science (American Association for the Advancement of Science) (16.05.1997)
Published in Science (American Association for the Advancement of Science) (16.05.1997)
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A novel insertional mutation in the prion protein gene: clinical and bio-molecular findings
Mauro, C, Giaccone, G, Piscosquito, G, Lavorgna, A, Nigro, M, Di Fede, G, Leonardi, A, Coppola, C, Formisano, S, Tagliavini, F, Cotrufo, R, Puoti, G
Published in Journal of neurology, neurosurgery and psychiatry (01.12.2008)
Published in Journal of neurology, neurosurgery and psychiatry (01.12.2008)
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Abandoned children and population genetics: the cases of Iggio and Tiola
Mazzoni, S., Nicolini, L., Tagliavini, F., Manfredini, M.
Published in Journal of Biological Research (15.11.2012)
Published in Journal of Biological Research (15.11.2012)
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Journal Article
Comparison of 2-D and 3-D computer models for the M. Salta rock fall, Vajont Valley, northern Italy
Tagliavini, F., Reichenbach, P., Maragna, D., Guzzetti, F., Pasuto, A.
Published in GeoInformatica (01.09.2009)
Published in GeoInformatica (01.09.2009)
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Journal Article
Conference Proceeding
An atypical case of sporadic fatal insomnia
Priano, L, Giaccone, G, Mangieri, M, Albani, G, Limido, L, Brioschi, A, Pradotto, L, Orsi, L, Mortara, P, Fociani, P, Mauro, A, Tagliavini, F
Published in Journal of neurology, neurosurgery and psychiatry (01.08.2009)
Published in Journal of neurology, neurosurgery and psychiatry (01.08.2009)
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Journal Article
Abandoned children and population genetics: the cases of Iggio and Tiola
S. Mazzoni, L. Nicolini, F. Tagliavini, M. Manfredini
Published in Journal of Biological Research (01.01.2012)
Published in Journal of Biological Research (01.01.2012)
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Journal Article
Site investigation and modelling at "La Maina" landslide (Carnian Alps, Italy)
Marcato, G., Mantovani, M., Pasuto, A., Silvano, S., Tagliavini, F., Zabuski, L., Zannoni, A.
Published in Natural hazards and earth system sciences (01.01.2006)
Published in Natural hazards and earth system sciences (01.01.2006)
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Familial frontotemporal dementia associated with the novel MAPT mutation T427M
Giaccone, Giorgio, Rossi, Giacomina, Farina, Laura, Marcon, Gabriella, Di Fede, Giuseppe, Catania, Marcella, Morbin, Michela, Sacco, Leonardo, Bugiani, Orso, Tagliavini, Fabrizio
Published in Journal of neurology (01.12.2005)
Published in Journal of neurology (01.12.2005)
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Journal Article
Evaluation of seismic effects on the landslide deposits of Monte Salta (Eastern Italian Alps) using distinct element method
Marcato, G., Fujisawa, K., Mantovani, M., Pasuto, A., Silvano, S., Tagliavini, F., Zabuski, L.
Published in Natural hazards and earth system sciences (01.01.2007)
Published in Natural hazards and earth system sciences (01.01.2007)
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A novel phenotype of sporadic Creutzfeldt–Jakob disease
Giaccone, G, Di Fede, G, Mangieri, M, Limido, L, Capobianco, R, Suardi, S, Grisoli, M, Binelli, S, Fociani, P, Bugiani, O, Tagliavini, F
Published in Journal of neurology, neurosurgery and psychiatry (01.12.2007)
Published in Journal of neurology, neurosurgery and psychiatry (01.12.2007)
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Amyloid protein of Gerstmann‐Sträussler‐Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N‐terminal glycine at codon 58
Tagliavini, F., Prelli, F., Ghiso, J., Bugiani, O., Serban, D., Prusiner, S. B., Farlow, M. R., Ghetti, B., Frangione, B.
Published in The EMBO journal (01.03.1991)
Published in The EMBO journal (01.03.1991)
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SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder
Del Dotto, Valentina, Ullah, Farid, Di Meo, Ivano, Magini, Pamela, Gusic, Mirjana, Maresca, Alessandra, Caporali, Leonardo, Palombo, Flavia, Tagliavini, Francesca, Baugh, Evan Harris, Macao, Bertil, Szilagyi, Zsolt, Peron, Camille, Gustafson, Margaret A, Khan, Kamal, La Morgia, Chiara, Barboni, Piero, Carbonelli, Michele, Valentino, Maria Lucia, Liguori, Rocco, Shashi, Vandana, Sullivan, Jennifer, Nagaraj, Shashi, El-Dairi, Mays, Iannaccone, Alessandro, Cutcutache, Ioana, Bertini, Enrico, Carrozzo, Rosalba, Emma, Francesco, Diomedi-Camassei, Francesca, Zanna, Claudia, Armstrong, Martin, Page, Matthew, Stong, Nicholas, Boesch, Sylvia, Kopajtich, Robert, Wortmann, Saskia, Sperl, Wolfgang, Davis, Erica E, Copeland, William C, Seri, Marco, Falkenberg, Maria, Prokisch, Holger, Katsanis, Nicholas, Tiranti, Valeria, Pippucci, Tommaso, Carelli, Valerio
Published in The Journal of clinical investigation (01.01.2020)
Published in The Journal of clinical investigation (01.01.2020)
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