Review: PrP 106‐126 – 25 years after by Forloni, G., Chiesa, R., Bugiani, O., Salmona, M., Tagliavini, F.

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The many ways to frontotemporal degeneration and beyond by Bugiani, O

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Tauopathy in human and experimental variant Creutzfeldt-Jakob disease by Giaccone, G, Mangieri, M, Capobianco, R, Limido, L, Hauw, J.J, Haïk, S, Fociani, P, Bugiani, O, Tagliavini, F

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A beta-related cerebral amyloid angiopathy by Bugiani, O

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Neuropathology of the dementias other than Alzheimer's by Bugiani, O

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Effectiveness of anthracycline against experimental prion disease in Syrian hamsters by 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

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Conformational polymorphism of the amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein by DE GIOIA, L, SELVAGGINI, C, GHIBAUDI, E, DIOMEDE, L, BUGIANI, O, FORLONI, G, TAGLIAVINI, F, SALMONA, M

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A -related cerebral amyloid angiopathy by Bugiani, O.

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Vascular Variant of Prion Protein Cerebral Amyloidosis with τ -Positive Neurofibrillary Tangles: The Phenotype of the Stop Codon 145 Mutation in PRNP by Ghetti, Bernardino, Piccardo, Pedro, Spillantini, Maria Grazia, Ichimiya, Yousuke, Porro, Monica, Perini, Francesco, Kitamoto, Tetsuyuki, Tateishi, Jun, Seiler, Charles, Frangione, Blas, Bugiani, Orso, Giaccone, Giorgio, Prelli, Frances, Goedert, Michel, Dlouhy, Stephen R., Tagliavini, Fabrizio

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CT and MR Imaging of Neuroaxonal Leukodystrophy Presenting as Early-Onset Frontal Dementia by Mascalchi, M, Gavazzi, C, Morbin, M, Giaccone, G, Arnetoli, G, Zappoli, R, Bugiani, O

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Staging/typing of Lewy body related α-synuclein pathology: a study of the BrainNet Europe Consortium by Alafuzoff, Irina, Ince, Paul G., Arzberger, Thomas, Al-Sarraj, Safa, Bell, Jeanne, Bodi, Istvan, Bogdanovic, Nenad, Bugiani, Orso, Ferrer, Isidro, Gelpi, Ellen, Gentleman, Stephen, Giaccone, Giorgio, Ironside, James W., Kavantzas, Nikolaos, King, Andrew, Korkolopoulou, Penelope, Kovács, Gábor G., Meyronet, David, Monoranu, Camelia, Parchi, Piero, Parkkinen, Laura, Patsouris, Efstratios, Roggendorf, Wolfgang, Rozemuller, Annemieke, Stadelmann-Nessler, Christine, Streichenberger, Nathalie, Thal, Dietmar R., Kretzschmar, Hans

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Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation by Baba, Y., Baker, M. C., Le Ber, I., Brice, A., Maeck, L., Kohlhase, J., Yasuda, M., Stoppe, G., Bugiani, O., Sperfeld, A. D., Tsuboi, Y., Uitti, R. J., Farrer, M. J., Ghetti, B., Hutton, M. L., Wszolek, Z. K.

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Familial frontotemporal dementia associated with the novel MAPT mutation T427M by Giaccone, Giorgio, Rossi, Giacomina, Farina, Laura, Marcon, Gabriella, Di Fede, Giuseppe, Catania, Marcella, Morbin, Michela, Sacco, Leonardo, Bugiani, Orso, Tagliavini, Fabrizio

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Assessment of β-amyloid deposits in human brain: a study of the BrainNet Europe Consortium by Alafuzoff, Irina, Thal, Dietmar R., Arzberger, Thomas, Bogdanovic, Nenad, Al-Sarraj, Safa, Bodi, Istvan, Boluda, Susan, Bugiani, Orso, Duyckaerts, Charles, Gelpi, Ellen, Gentleman, Stephen, Giaccone, Giorgio, Graeber, Manuel, Hortobagyi, Tibor, Höftberger, Romana, Ince, Paul, Ironside, James W., Kavantzas, Nikolaos, King, Andrew, Korkolopoulou, Penelope, Kovács, Gábor G., Meyronet, David, Monoranu, Camelia, Nilsson, Tatjana, Parchi, Piero, Patsouris, Efstratios, Pikkarainen, Maria, Revesz, Tamas, Rozemuller, Annemieke, Seilhean, Danielle, Schulz-Schaeffer, Walter, Streichenberger, Nathalie, Wharton, Stephen B., Kretzschmar, Hans

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A Neurotoxic and Gliotrophic Fragment of the Prion Protein Increases Plasma Membrane Microviscosity by Salmona, M., Forloni, G., Diomede, L., Algeri, M., De Gioia, L., Angeretti, N., Giaccone, G., Tagliavini, F., Bugiani, O.

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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 by Tagliavini, F., Prelli, F., Ghiso, J., Bugiani, O., Serban, D., Prusiner, S. B., Farlow, M. R., Ghetti, B., Frangione, B.

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FVEPs in Creutzfeldt–Jacob disease: waveforms and interaction with the periodic EEG pattern assessed by single sweep analysis by Visani, E., Agazzi, P., Scaioli, V., Giaccone, G., Binelli, S., Canafoglia, L., Panzica, F., Tagliavini, F., Bugiani, O., Avanzini, G., Franceschetti, S.

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Substitutions at Codon 22 of Alzheimer's Aβ Peptide Induce Diverse Conformational Changes and Apoptotic Effects in Human Cerebral Endothelial Cells by Miravalle, Leticia, Tokuda, Takahiko, Chiarle, Roberto, Giaccone, Giorgio, Bugiani, Orso, Tagliavini, Fabrizio, Frangione, Blas, Ghiso, Jorge

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APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38 by Moro, Maria Luisa, Giaccone, Giorgio, Lombardi, Raffaella, Indaco, Antonio, Uggetti, Andrea, Morbin, Michela, Saccucci, Stefania, Di Fede, Giuseppe, Catania, Marcella, Walsh, Dominic M., Demarchi, Andrea, Rozemuller, Annemieke, Bogdanovic, Nenad, Bugiani, Orso, Ghetti, Bernardino, Tagliavini, Fabrizio

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Frontotemporal Dementia and Corticobasal Degeneration in a Family with a P301S Mutation in Tau by Bugiani, Orso, Murrell, Jill R, Giaccone, Giorgio, Hasegawa, Masato, Ghigo, Giuseppe, Tabaton, Massimo, Morbin, Michela, Primavera, Alberto, Carella, Francesco, Solaro, Claudio, Grisoli, Marina, Savoiardo, Mario, Spillantini, Maria Grazia, Tagliavini, Fabrizio, Goedert, Michel, Ghetti, Bernardino

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