119 Publications (Page 3 of 5)
2008
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 mutationsMaarouf, 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, (no. 1), pp. 20, 2008-Nov-20.
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Iron-mediated Aggregation and a Localized Structural Change Characterize Ferritin from a Mutant Light Chain Polypeptide That Causes Neurodegeneration *Baraibar, Martin A⋅Barbeito, Ana G⋅Muhoberac, Barry B and Vidal, RubenJournal of Biological Chemistry, vol. 283, (no. 46), pp. 31679-31689, 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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2007
Clinicopathologic features of frontotemporal dementia with Progranulin sequence variationSpina, Salvatore⋅Murrell, Jill R⋅Huey, ED⋅Wassermann, Eric⋅Pietrini, Pietro⋅Baraibar, MA⋅Barbeito, AG⋅Troncoso, Juan C⋅Vidal, Ruben G⋅Ghetti, Bernardino and Grafman, JordanNeurology, vol. 68, (no. 11), pp. 820-827, 2007.
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2005
Amino-terminally truncated Abeta peptide species are the main component of cotton wool plaquesMiravalle, Leticia⋅Miravalle, Leticia⋅Calero, Miguel⋅Calero, Miguel⋅Takao, Masaki⋅Takao, Masaki⋅Roher, Alex E⋅Roher, Alex E⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Vidal, Ruben and Vidal, RubenBiochemistry, vol. 44, (no. 32), pp. 10810, 2005-Aug-16.
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Amino-Terminally Truncated Aβ Peptide Species Are the Main Component of Cotton Wool PlaquesMiravalle, Leticia⋅Miravalle, Leticia⋅Calero, Miguel⋅Calero, Miguel⋅Takao, Masaki⋅Takao, Masaki⋅Roher, Alex E⋅Roher, Alex E⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Vidal, Ruben and Vidal, RubenBiochemistry, vol. 44, (no. 32), pp. 10821, 20050816.
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2004
Axonal transport of British and Danish amyloid peptides via secretory vesicles.Choi, Seung-Il⋅Vidal, Ruben G⋅Frangione, Blas and Levy, EfratThe FASEB journal : official publication of the Federation of American Societies for Experimental Biology, vol. 18, (no. 2), pp. 373-5, 2004/Feb.
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Early‐onset Dementia with Lewy BodiesTakao, Masaki⋅Takao, Masaki⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Yoshida, Hirotaka⋅Yoshida, Hirotaka⋅Piccardo, Pedro⋅Piccardo, Pedro⋅Narain, Yolanda⋅Narain, Yolanda⋅Murrell, Jill R⋅Murrell, Jill R⋅Vidal, Ruben⋅Vidal, Ruben⋅Glazier, Bradley S⋅Glazier, Bradley S⋅Jakes, Ross⋅Jakes, Ross⋅Tsutsui, Miho⋅Tsutsui, Miho⋅Spillantini, Maria G⋅Spillantini, Maria Grazia⋅Crowther, R A⋅Crowther, R. Anthony⋅Goedert, Michel⋅Goedert, Michel⋅Koto, Atsuo and Koto, AtsuoBrain Pathology, vol. 14, (no. 2), pp. 147, April 2004.
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Immunolocalization of the Oligodendrocyte Transcription Factor 1 (Olig1) in Brain TumorsAzzarelli, Biagio⋅Azzarelli, Biagio⋅Miravalle, Leticia⋅Miravalle, Leticia⋅Vidal, Ruben and Vidal, RubenJNEN: Journal of Neuropathology & Experimental Neurology, vol. 63, (no. 2), pp. 179, 2004-February.
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Intracellular Ferritin Accumulation in Neural and Extraneural Tissue Characterizes a Neurodegenerative Disease Associated with a Mutation in the Ferritin Light Polypeptide GeneVidal, Ruben G⋅Ghetti, Bernardino⋅Takao, M.⋅Brefel-Courbon, C.⋅Uro-Coste, E.⋅Glazier, BS⋅Siani, V.⋅Benson, Merrill D⋅Calvas, P.⋅Miravalle, L.⋅Rascol, O. and Delisle, MBJournal of Neuropathology & Experimental Neurology, vol. 63, (no. 4), pp. 363-380, 2004.
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Intracellular Ferritin Accumulation in Neural and Extraneural Tissue Characterizes a Neurodegenerative Disease Associated with a Mutation in the Ferritin Light Polypeptide GeneVidal, R⋅Ghetti, B⋅Takao, M and Brefel-Courbon, C(pp. 363-80). Apr 2004
Neurodegeneration caused by proteins with an aberrant carboxyl-terminus.Vidal, Ruben G⋅Delisle, Marie B and Ghetti, BernardinoJournal of neuropathology and experimental neurology. , vol. 63, (no. 8), pp. 787-800, 2004/Aug.
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P1-216 Cotton wool plaques associated with a novel mutation in the presenilin 1 gene (V261I): immunohistological, genetic and biochemicals studiesMiravalle, Leticia⋅Miravalle, Leticia⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Calero, Miguel⋅Calero, Miguel⋅Rentz, Clarissa A⋅Rentz, Clarissa A⋅Richardson, Rose M⋅Richardson, Rose M⋅Takao, Masaki⋅Takao, Masaki⋅Vidal, Ruben and Vidal, RubenNeurobiology of Aging, vol. 25, pp. S157, 2004.
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P4-242 Oxidative damage in ferritin-induced neurodegenerationVidal, Ruben⋅Vidal, Ruben⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Delisle, Marie B⋅Delisle, Marie B⋅Rascol, Olivier⋅Rascol, Olivier⋅Perry, George⋅Perry, George⋅Smith, Mark A and Smith, Mark ANeurobiology of Aging, vol. 25, pp. S544, 2004.
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The human amyloid-beta precursor protein770 mutation V717F generates peptides longer than amyloid-beta-(40-42) and flocculent amyloid aggregatesRoher, Alex E⋅Roher, Alex E⋅Kokjohn, Tyler A⋅Kokjohn, Tyler A⋅Esh, Chera⋅Esh, Chera⋅Weiss, Nicole⋅Weiss, Nicole⋅Childress, Jennifer⋅Childress, Jennifer⋅Kalback, Walter⋅Kalback, Walter⋅Luehrs, Dean C⋅Luehrs, Dean C⋅Lopez, John⋅Lopez, John⋅Brune, Daniel⋅Brune, Daniel⋅Kuo, Yu-Min⋅Kuo, Yu-Min⋅Farlow, Martin⋅Farlow, Martin⋅Murrell, Jill⋅Murrell, Jill⋅Vidal, Ruben⋅Vidal, Ruben⋅Ghetti, Bernardino and Ghetti, BernardinoThe Journal of biological chemistry, vol. 279, (no. 7), pp. 5836, 2004-Feb-13.
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2003
Hereditary ferritinopathyVidal, Ruben⋅Vidal, Ruben⋅Delisle, Marie Bernadette⋅Delisle, Marie Bernadette⋅Rascol, Olivier⋅Rascol, Olivier⋅Ghetti, Bernardino and Ghetti, BernardinoJournal of the Neurological Sciences, vol. 207, (no. 1), pp. 111, 2003.
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Hereditary ferritinopathy.Vidal, Ruben⋅Delisle, Marie Bernadette⋅Rascol, Olivier and Ghetti, BernardinoJournal of the neurological sciences, vol. 207, (no. 1-2), pp. 110-111, March 15, 2003.
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Hereditary ferritinopathy.Vidal, Ruben G⋅Delisle, Marie B⋅Rascol, Olivier and Ghetti, BernardinoJournal of the neurological sciences. , vol. 207, (no. 1-2), pp. 110-1, 2003/Mar/15.
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