508 Publications (Page 10 of 21)
2009
Failure to detect the presence of prions in the uterine and gestational tissues from a Gravida with Creutzfeldt-Jakob disease.Xiao, Xiangzhu⋅Miravalle, Leticia⋅Yuan, Jue⋅McGeehan, John⋅Dong, Zhiqian⋅Wyza, Robert⋅Mac Lennan, Gregory⋅Golichowski, Alan M⋅Kneale, Geoff⋅King, Nicholas⋅Kong, Qingzhong⋅Spina, Salvatore⋅Vidal, Ruben G⋅Ghetti, Bernardino⋅Roos, Karen⋅Gambetti, Pierluigi and Zou, Wen QuanThe American journal of pathology, vol. 174, (no. 5), pp. 1602-8, 2009/May.
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Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification.Parchi, Piero⋅Strammiello, Rosaria⋅Notari, Silvio⋅Giese, Armin⋅Langeveld, Jan P⋅Ladogana, Anna⋅Zerr, Inga⋅Roncaroli, Federico⋅Cras, Patrich⋅Ghetti, Bernardino⋅Pocchiari, Maurizio⋅Kretzschmar, Hans and Capellari, SabinaActa neuropathologica, vol. 118, (no. 5), pp. 659-71, 2009/Nov.
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Mutant presenilin 1 increases the expression and activity of BACE1.Giliberto, Luca⋅Borghi, Roberta⋅Piccini, Alessandra⋅Mangerini, Rosa⋅Sorbi, Sandro⋅Cirmena, Gabriella⋅Garuti, Anna⋅Ghetti, Bernardino⋅Tagliavini, Fabrizio⋅Mughal, Mohamed R⋅Mattson, Mark P⋅Zhu, Xiongwei⋅Wang, Xinglong⋅Guglielmotto, Michela⋅Tamagno, Elena and Tabaton, MassimoThe Journal of biological chemistry, vol. 284, (no. 14), pp. 9027-9038, April 3, 2009.
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Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendationsMackenzie, Ian R A⋅Mackenzie, Ian⋅Neumann, Manuela⋅Neumann, Manuela⋅Bigio, Eileen H⋅Bigio, Eileen H⋅Cairns, Nigel J⋅Cairns, Nigel⋅Alafuzoff, Irina⋅Alafuzoff, Irina⋅Kril, Jillian⋅Kril, Jillian⋅Kovacs, Gabor G⋅Kovacs, Gabor G⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Halliday, Glenda M⋅Halliday, Glenda⋅Holm, Ida E⋅Holm, Ida E⋅Ince, Paul G⋅Ince, Paul G⋅Kamphorst, Wouter⋅Kamphorst, Wouter⋅Revesz, Tamas⋅Revesz, Tamas⋅Rozemuller, Annemieke J M⋅Rozemuller, Annemieke J⋅Kumar-Singh, Samir⋅Kumar-Singh, Samir⋅Akiyama, Haruhiko⋅Akiyama, Haruhiko⋅Baborie, Atik⋅Baborie, Atik⋅Spina, Salvatore⋅Spina, Salvatore⋅Dickson, Dennis W⋅Dickson, Dennis W⋅Trojanowski, John Q⋅Trojanowski, John Q⋅Mann, David M A and Mann, DavidActa Neuropathologica, vol. 117, (no. 1), pp. 15-18, 2009.
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Old Age Before Cognitive ImpairmentGhetti, BernardinoCurrent Alzheimer Research, vol. 6, (no. 4), pp. 323-323, 2009.
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P4‐241: Novel TARDBP mutation associated with frontotemporal dementia and movement disorder but not motor neuron diseaseKovacs, Gabor G⋅Murrell, Jill R⋅Horvath, Sandor⋅Haraszti, Laszlo⋅Majtenyi, Katalin⋅Budka, Herbert⋅Ghetti, Bernardino and Spina, SalvatoreAlzheimer's & Dementia, vol. 5, (no. 4S_Part_16), pp. P501, July 2009.
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Regional differences in the vulnerability of substantia nigra dopaminergic neurons in weaver miceMarti, Joaquim⋅Marti, Joaquín⋅Santa-Cruz, MC⋅Santa-Cruz, María C⋅Molina, V.⋅Molina, Vanessa⋅Serra, R.⋅Serra, Roger⋅Bayer, SA⋅Bayer, Shirley A⋅Ghetti, Bernardino⋅Ghetti, B.⋅Hervás, José P and Hervas, JPActa neurobiologiae experimentalis, vol. 69, (no. 2), pp. 198, 2009-00-00.
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TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and choreaKovacs, Gabor G⋅Kovacs, Gabor G⋅Kovacs, Gabor G⋅Murrell, Jill R⋅Murrell, Jill R⋅Murrell, Jill R⋅Horvath, Sandor⋅Horvath, Sandor⋅Horvath, Sandor⋅Haraszti, Laszlo⋅Haraszti, Laszlo⋅Haraszti, Laszlo⋅Majtenyi, Katalin⋅Majtenyi, Katalin⋅Majtenyi, Katalin⋅Molnar, Maria J⋅Molnar, Maria J⋅Molnar, Maria J⋅Budka, Herbert⋅Budka, Herbert⋅Budka, Herbert⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Spina, Salvatore⋅Spina, Salvatore and Spina, SalvatoreMovement disorders : official journal of the Movement Disorder Society, vol. 24, (no. 12), pp. 1843, 2009-Sep-15.
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2008
Aggregated, wild-type prion protein causes neurological dysfunction and synaptic abnormalities.Chiesa, Roberto⋅Piccardo, Pedro⋅Biasini, Emiliano⋅Ghetti, Bernardino and Harris, David AThe Journal of neuroscience : the official journal of the Society for Neuroscience, vol. 28, (no. 49), pp. 13258-67, 2008/Dec/3.
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Analysis of tau phosphorylation and truncation in a mouse model of human tauopathy.Delobel, Patrice⋅Lavenir, Isabelle⋅Fraser, Graham⋅Ingram, Esther⋅Holzer, Max⋅Ghetti, Bernardino⋅Spillantini, Maria G⋅Crowther, R A and Goedert, MichelThe American journal of pathology, vol. 172, (no. 1), pp. 123-31, 2008/Jan.
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Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease.Notari, Silvio⋅Strammiello, Rosaria⋅Capellari, Sabina⋅Giese, Armin⋅Cescatti, Maura⋅Grassi, Jacques⋅Ghetti, Bernardino⋅Langeveld, Jan P⋅Zou, Wen Quan⋅Gambetti, Pierluigi⋅Kretzschmar, Hans A and Parchi, PieroThe Journal of biological chemistry, vol. 283, (no. 45), pp. 30557-65, 2008/Nov/7.
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Detection of filamentous tau inclusions by the fluorescent Congo red derivative FSB [(trans,trans)-1-fluoro-2,5-bis(3-hydroxycarbonyl-4-hydroxy)styrylbenzene].Velasco, Ana⋅Fraser, Graham⋅Delobel, Patrice⋅Ghetti, Bernardino⋅Lavenir, Isabelle and Goedert, MichelFEBS letters, vol. 582, (no. 6), pp. 901-906, March 19, 2008.
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Expression of a Mutant Form of the Ferritin Light Chain Gene Induces Neurodegeneration and Iron Overload in Transgenic MiceVidal, Ruben G⋅Miravalle, Leticia⋅Gao, Xiaoying⋅Barbeito, Ana G⋅Baraibar, Martin A⋅Hekmatyar, Shahryar K⋅Widel, Mario⋅Bansal, Navin⋅Delisle, Marie B and Ghetti, BernardinoJournal of Neuroscience, vol. 28, (no. 1), pp. 60-67, 2008.
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Histopathological and molecular heterogeneity among individuals with dementia associated with Presenilin mutations.Maarouf, Chera L⋅Maarouf, Chera L⋅Maarouf, Chera L⋅Daugs, Ian D⋅Daugs, Ian D⋅Daugs, Ian D⋅Spina, Salvatore⋅Spina, Salvatore⋅Spina, Salvatore⋅Vidal, Ruben⋅Vidal, Ruben⋅Vidal, Ruben⋅Kokjohn, Tyler A⋅Kokjohn, Tyler A⋅Kokjohn, Tyler A⋅Patton, R Lyle⋅Patton, R Lyle⋅Patton, R Lyle⋅Kalback, Walter M⋅Kalback, Walter M⋅Kalback, Walter M⋅Luehrs, Dean C⋅Luehrs, Dean C⋅Luehrs, Dean C⋅Walker, Douglas G⋅Walker, Douglas G⋅Walker, Douglas G⋅Castaño, Eduardo M⋅Castaño, Eduardo M⋅Castaño, Eduardo M⋅Beach, Thomas G⋅Beach, Thomas G⋅Beach, Thomas G⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Roher, Alex E⋅Roher, Alex E and Roher, Alex EMolecular neurodegeneration, vol. 3, pp. 20, November 20, 2008.
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In vivo and postmortem clinicoanatomical correlations in frontotemporal dementia and parkinsonism linked to chromosome 17.Ghetti, Bernardino⋅Ghetti, Bernardino⋅Spina, Salvatore⋅Spina, Salvatore⋅Murrell, Jill R⋅Murrell, Jill R⋅Huey, Edward D⋅Huey, Edward D⋅Pietrini, Pietro⋅Pietrini, Pietro⋅Sweeney, Brian⋅Sweeney, Brian⋅Wassermann, Eric M⋅Wassermann, Eric M⋅Keohane, Catherine⋅Keohane, Catherine⋅Farlow, Martin R⋅Farlow, Martin R⋅Grafman, Jordan H and Grafman, JordanNeuro-degenerative diseases, vol. 5, (no. 3-4), pp. 215-7, 2008.
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O2-05-03: Inclusion body myopathy with paget disease of the bone and frontotemporal dementia: New families, a novel mutation, and a new clinical presentationSpina, Salvatore⋅Spina, Salvatore⋅Van Laar, Amber⋅Van Laar, Amber⋅Murrell, Jill⋅Murrell, Jill⋅Courten-Myers, Gabrielle⋅Courten-Myers, Gabrielle⋅Hamilton, Ronald⋅Hamilton, Ronald⋅Vidal, Ruben⋅Vidal, Ruben⋅Farlow, Martin⋅Farlow, Martin⋅Quinlan, John⋅Quinlan, John⋅DeKosky, Steven⋅DeKosky, Steven⋅Ghetti, Bernardino and Ghetti, BernardinoAlzheimer's & Dementia: The Journal of the Alzheimer's Association, vol. 4, (no. 4), pp. T141, 2008.
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O3-01-04: Vascular amyloid deposition and related pathology in a transgenic mouse model of familial Danish dementiaVidal, Ruben⋅Vidal, Ruben⋅Barbeito, Ana⋅Barbeito, Ana⋅Miravalle, Leticia⋅Miravalle, Leticia⋅Ghetti, Bernardino and Ghetti, BernardinoAlzheimer's & Dementia: The Journal of the Alzheimer's Association, vol. 4, (no. 4), pp. T158, 2008.
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P1-105: Neurodegeneration and iron overload in transgenic mice expressing a mutant form of the ferritin light polypeptide geneVidal, Ruben⋅Vidal, Ruben⋅Miravalle, Leticia⋅Miravalle, Leticia⋅Barbeito, Ana⋅Barbeito, Ana⋅Baraibar, Martin⋅Baraibar, Martin⋅Bansal, Navin⋅Bansal, Navin⋅Smith, Mark⋅Smith, Mark⋅Delisle, Marie⋅Delisle, Marie⋅Ghetti, Bernardino and Ghetti, BernardinoAlzheimer's & Dementia: The Journal of the Alzheimer's Association, vol. 4, (no. 4), pp. T237, 2008.
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P2-205: Neuropathologic and genetic characterization of frontotemporal lobar degeneration with ubiquitin- and/or TDP-43-positive inclusions: A large seriesSpina, Salvatore⋅Spina, Salvatore⋅Murrell, Jill⋅Murrell, Jill⋅Vidal, Ruben⋅Vidal, Ruben⋅Ghetti, Bernardino and Ghetti, BernardinoAlzheimer's & Dementia: The Journal of the Alzheimer's Association, vol. 4, (no. 4), pp. T431, 2008.
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P3-221: Familial Alzheimer's disease associated with the V717L amyloid precursor protein gene mutation: Neuropathological characterizationGhetti, Bernardino⋅Ghetti, Bernardino⋅Hake, Ann⋅Hake, Ann⋅Murrell, Jill⋅Murrell, Jill⋅Epperson, Francine⋅Epperson, Francine⋅Farlow, Martin⋅Farlow, Martin⋅Vidal, Ruben⋅Vidal, Ruben⋅Spina, Salvatore and Spina, SalvatoreAlzheimer's & Dementia: The Journal of the Alzheimer's Association, vol. 4, (no. 4), pp. T585, 2008.
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Presenilin-1 280Glu-->Ala mutation alters C-terminal APP processing yielding longer abeta peptides: implications for Alzheimer's diseaseVan Vickle, Gregory D⋅Van Vickle, Gregory D⋅Esh, Chera L⋅Esh, Chera L⋅Kokjohn, Tyler A⋅Kokjohn, Tyler A⋅Patton, R Lyle⋅Patton, R Lyle⋅Kalback, Walter M⋅Kalback, Walter M⋅Luehrs, Dean C⋅Luehrs, Dean C⋅Beach, Thomas G⋅Beach, Thomas G⋅Newel, Amanda J⋅Newel, Amanda J⋅Lopera, Francisco⋅Lopera, Francisco⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Vidal, Ruben⋅Vidal, Ruben⋅Castaño, Eduardo M⋅Castaño, Eduardo M⋅Roher, Alex E and Roher, Alex EMolecular medicine (Cambridge, Mass.), vol. 14, (no. 3-4), pp. 184, 2008 Mar-Apr.
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Presenilin-1 280Glu→Ala Mutation Alters C-Terminal APP Processing Yielding Longer Aβ Peptides: Implications for Alzheimer’s DiseaseVan Vickle, Gregory D⋅Van Vickle, Gregory D⋅Esh, Chera L⋅Esh, Chera L⋅Kokjohn, Tyler A⋅Kokjohn, Tyler A⋅Patton, R. Lyle⋅Patton, R. Lyle⋅Kalback, Walter M⋅Kalback, Walter M⋅Luehrs, Dean C⋅Luehrs, Dean C⋅Beach, Thomas G⋅Beach, Thomas G⋅Newel, Amanda J⋅Newel, Amanda J⋅Lopera, Francisco⋅Lopera, Francisco⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Vidal, Ruben⋅Vidal, Ruben⋅Castaño, Eduardo M⋅Castaño, Eduardo M⋅Roher, Alex E and Roher, Alex EMolecular Medicine, vol. 14, (no. 3-4), pp. 194, 2008-03-00.
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The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD familySpina, Salvatore⋅Spina, Salvatore⋅Farlow, Martin R⋅Farlow, Martin R⋅Unverzagt, Frederick W⋅Unverzagt, Frederick⋅Kareken, David A⋅Kareken, David A⋅Murrell, Jill R⋅Murrell, Jill R⋅Fraser, Graham⋅Fraser, Graham⋅Epperson, Francine⋅Epperson, Francine⋅Crowther, R Anthony⋅Crowther, RAnthony⋅Spillantini, Maria G⋅Spillantini, Maria G⋅Goedert, Michel⋅Goedert, Michel⋅Ghetti, Bernardino and Ghetti, BernardinoBrain, vol. 131, (no. 1), pp. 72-89, 2008.
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White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration.Kovacs, Gabor G⋅Kovacs, Gabor G⋅Majtenyi, Katalin⋅Majtenyi, Katalin⋅Spina, Salvatore⋅Spina, Salvatore⋅Murrell, Jill R⋅Murrell, Jill R⋅Gelpi, Ellen⋅Gelpi, Ellen⋅Hoftberger, Romana⋅Hoftberger, Romana⋅Fraser, Graham⋅Fraser, Graham⋅Crowther, R A⋅Crowther, R A⋅Goedert, Michel⋅Goedert, Michel⋅Budka, Herbert⋅Budka, Herbert⋅Ghetti, Bernardino and Ghetti, BernardinoJournal of neuropathology and experimental neurology, vol. 67, (no. 10), pp. 963-75, 2008/Oct.
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2007
Accumulation of prion protein in the brain that is not associated with transmissible disease.Piccardo, Pedro⋅Manson, Jean C⋅King, Declan⋅Ghetti, Bernardino and Barron, Rona MProceedings of the National Academy of Sciences of the United States of America, vol. 104, (no. 11), pp. 4712-4717, March 13, 2007.
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