Resultados de procura - Orso Bugiani

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  1. 1
    Why is delirium more frequent in the elderly?

    Why is delirium more frequent in the elderly? por Orso Bugiani

    Publicado 2021
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  2. 2
    Progressive supranuclear palsy 1979: an overview

    Progressive supranuclear palsy 1979: an overview por A Brusa, Gianluigi Mancardi, Orso Bugiani

    Publicado 1979
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  3. 3
    Presence of Reactive Microglia and Neuroinflammatory Mediators in a Case of Frontotemporal Dementia with P301S Mutation

    Presence of Reactive Microglia and Neuroinflammatory Mediators in a Case of Frontotemporal Dementia with P301S Mutation por Arianna Bellucci, Orso Bugiani, Bernardino Ghetti, Maria Grazia Spillantini

    Publicado 2011
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  4. 4
    Substitutions at Codon 22 of Alzheimer's Aβ Peptide Induce Diverse Conformational Changes and Apoptotic Effects in Human Cerebral Endothelial Cells

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

    Publicado 2000
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  5. 5
    Conformational polymorphism of the amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein.

    Conformational polymorphism of the amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein. por Luca De Gioia, Carlo Selvaggini, Elena Ghibaudi, Luisa Diomede, Orso Bugiani, Gianluigi Forloni, Fabrizio Tagliavini, Mario Salmona

    Publicado 1994
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  6. 6
    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.

    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. por Fabrizio Tagliavini, Frances Prelli, Jorge Ghiso, Orso Bugiani, D. Serban, Stanley B. Prusiner, Martin R. Farlow, Bernardino Ghetti, Blas Frangione

    Publicado 1991
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  7. 7
    Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred.

    Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred. por Giorgio Giaccone, Laura Verga, Orso Bugiani, B Frangione, D. Serban, Stanley B. Prusiner, Martin R. Farlow, Bernardino Ghetti, Fabrizio Tagliavini

    Publicado 1992
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  8. 8
    Prion Protein Amyloidosis

    Prion Protein Amyloidosis por Bernardino Ghetti, Pedro Piccardo, B Frangione, Orso Bugiani, Giorgio Giaccone, Katherine Young, Frances Prelli, Martin R. Farlow, Stephen R. Dlouhy, Fabrizio Tagliavini

    Publicado 1996
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  9. 9
    Molecular determinants of the physicochemical properties of a critical prion protein region comprising residues 106–126

    Molecular determinants of the physicochemical properties of a critical prion protein region comprising residues 106–126 por Mario Salmona, Paolo MALESANI, Luca DE GIOIA, Stefano GORLA, Maurizio Bruschi, Agnese Molinari, Franco DELLA VEDOVA, Barbara PEDROTTI, Maria Anna MARRARI, Tazeen AWAN, Orso Bugiani, Gianluigi Forloni, Fabrizio Tagliavini

    Publicado 1999
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  10. 10
    A 7-kDa Prion Protein (PrP) Fragment, an Integral Component of the PrP Region Required for Infectivity, Is the Major Amyloid Protein in Gerstmann-Sträussler-Scheinker Disease A117V

    A 7-kDa Prion Protein (PrP) Fragment, an Integral Component of the PrP Region Required for Infectivity, Is the Major Amyloid Protein in Gerstmann-Sträussler-Scheinker Disease A117V... por Fabrizio Tagliavini, Patricia Lievens, Christine Tranchant, Jean-Marie Warter, Michel Mohr, Giorgio Giaccone, Francesco Perini, Giacomina Rossi, Mario Salmona, Pedro Piccardo, Bernardino Ghetti, Ronald C. Beavis, Orso Bugiani, Blas Frangione, Frances Prelli

    Publicado 2001
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  11. 11
    Frontotemporal Dementia and Corticobasal Degeneration in a Family with a P301S Mutation in Tau

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

    Publicado 1999
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  12. 12
    Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

    Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP. por Bernardino Ghetti, Pedro Piccardo, Maria Grazia Spillantini, Y Ichimiya, M. Porro, Francesco Perini, Tetsuyuki Kitamoto, Jun Tateishi, Charles E. Seiler, B Frangione, Orso Bugiani, Giorgio Giaccone, Frances Prelli, Michel Goedert, S. R. Dlouhy, Fabrizio Tagliavini

    Publicado 1996
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  13. 13
    Structural Properties of Gerstmann-Sträussler-Scheinker Disease Amyloid Protein

    Structural Properties of Gerstmann-Sträussler-Scheinker Disease Amyloid Protein por Mario Salmona, Michela Morbin, Tania Massignan, Laura Colombo, Giulia Mazzoleni, Raffaella Capobianco, Luisa Diomede, Florian Thaler, Luca Mollica, Giovanna Musco, Joseph J. Kourie, Orso Bugiani, Deepak Sharma, Hideyo Inouye, Daniel A. Kirschner, Gianluigi Forloni, Fabrizio Tagliavini

    Publicado 2003
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  14. 14
    Tetracyclines affect prion infectivity

    Tetracyclines affect prion infectivity por Gianluigi Forloni, Selina Iussich, Tazeen Awan, Laura Colombo, Nadia Angeretti, Laura Girola, Ilaria Bertani, G. Poli, Maria Caramelli, Maria Grazia Bruzzone, Laura Farina, Lucia Limido, Giacomina Rossi, Giorgio Giaccone, James W. Ironside, Orso Bugiani, Mario Salmona, Fabrizio Tagliavini

    Publicado 2002
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  15. 15
    Prion Proteins with Different Conformations Accumulate in Gerstmann-Sträussler-Scheinker Disease Caused by A117V and F198S Mutations

    Prion Proteins with Different Conformations Accumulate in Gerstmann-Sträussler-Scheinker Disease Caused by A117V and F198S Mutations por Pedro Piccardo, Juris J. Liepnieks, Albert William, Stephen R. Dlouhy, Martin R. Farlow, Katherine Young, David Nochlin, Thomas D. Bird, Randal R. Nixon, Melvyn J. Ball, Charles DeCarli, Orso Bugiani, Fabrizio Tagliavini, Merrill D. Benson, Bernardino Ghetti

    Publicado 2001
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  16. 16
    Neuropathological Diagnostic Criteria for Creutzfeldt‐Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases)

    Neuropathological Diagnostic Criteria for Creutzfeldt‐Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases) por Herbert Budka, Adriano Aguzzi, Paul Brown, Jean‐Marie Brucher, Orso Bugiani, F. Gullotta, Matti Haltia, Jean‐Jacques Hauw, James W. Ironside, K. A. Jellinger, Hans A. Kretzschmar, P. L. Lantos, Carlo Masullo, W. Schlote, Jun Tateishi, Roy O. Weller

    Publicado 1995
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  17. 17
    Tissue Handling in Suspected Creutzfeldt‐Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases)

    Tissue Handling in Suspected Creutzfeldt‐Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases) por Herbert Budka, Adriano Aguzzi, Paul Brown, Jean‐Marie Brucher, Orso Bugiani, John Collinge, Heino Diringer, F. Gullotta, Matti Haltia, Jean‐Jacques Hauw, James W. Ironside, Hans A. Kretzschmar, P. L. Lantos, Carlo Masullo, Maurizio Pocchiari, W. Schlote, Jun Tateishi, Robert Will

    Publicado 1995
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  18. 18
    Hereditary Cerebral Hemorrhage With Amyloidosis Associated With the E693K Mutation of APP

    Hereditary Cerebral Hemorrhage With Amyloidosis Associated With the E693K Mutation of APP por Orso Bugiani, Giorgio Giaccone, Giacomina Rossi, Michela Mangieri, Raffaella Capobianco, Michela Morbin, Giulia Mazzoleni, Chiara Cupidi, Gabriella Marcon, Anna Rıta Gıovagnolı, Alberto Bizzi, Giuseppe Di Fede, Gianfranco Puoti, F. Carella, Andrea Salmaggi, A. Romorini, G. Patruno, Mauro Magoni, Alessandro Padovani, Fabrizio Tagliavini

    Publicado 2010
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  19. 19
    Phenotypic Variability of Gerstmann-Straussler-Scheinker Disease is Associated with Prion Protein Heterogeneity

    Phenotypic Variability of Gerstmann-Straussler-Scheinker Disease is Associated with Prion Protein Heterogeneity por Pedro Piccardo, Stephen R. Dlouhy, Patricia Lievens, Katherine Young, Thomas D. Bird, David Nochlin, Dennis W. Dickson, Harry V. Vinters, Thomas Zimmerman, Ian R. Mackenzie, Stephen J. Kish, Lee‐Cyn Ang, Charles De Carli, Maurizio Pocchiari, Paul Brown, Clarence J. Gibbs, D. C. Gajdusek, Orso Bugiani, James W. Ironside, Fabrizio Tagliavini, Bernardino Ghetti

    Publicado 1998
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  20. 20
    Staging of Neurofibrillary Pathology in Alzheimer's Disease: A Study of the BrainNet Europe Consortium

    Staging of Neurofibrillary Pathology in Alzheimer's Disease: A Study of the BrainNet Europe Consortium por Irina Alafuzoff, Thomas Arzberger, Safa Al‐Sarraj, István Bódi, Nenad Bogdanović, Heiko Braak, Orso Bugiani, Kelly Del‐Tredici, Isidró Ferrer, Ellen Gelpí, Giorgio Giaccone, Manuel B. Graeber, Paul G. Ince, Wouter Kamphorst, Andrew King, Penelope Korkolopoulou, Gábor G. Kovács, Sergey Larionov, David Meyronet, Camelia Monoranu, Piero Parchi, Efstratios Patsouris, Wolfgang Roggendorf, Danielle Seilhean, Fabrizio Tagliavini, Christine Stadelmann, Nathalie Streichenberger, Dietmar Rudolf Thal, Stephen B. Wharton, Hans Kretzschmar

    Publicado 2008
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