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Bernardino Ghetti

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Huey Edward D; Pardini Matteo; Cavanagh Alyson; Wassermann Eric M; Kapogiannis Dimitrios; Spina Salvatore; Ghetti Bernardino; Grafman Jordan
Association of ideomotor apraxia with frontal gray matter volume loss in corticobasal syndrome.
Kovacs Gabor G; Murrell Jill R; Horvath Sandor; Haraszti Laszlo; Majtenyi Katalin; Molnar Maria J; Budka Herbert; Ghetti Bernardino; Spina Salvatore
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.
Ghetti Bernardino
Old age before cognitive impairment.

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All Publications

2009: Huey Edward D; Pardini Matteo; Cavanagh Alyson; Wassermann Eric M; Kapogiannis Dimitrios; Spina Salvatore; Ghetti Bernardino; Grafman Jordan
Association of ideomotor apraxia with frontal gray matter volume loss in corticobasal syndrome.
Archives of neurology 2009;66(10):1274-80.
2009: Kovacs Gabor G; Murrell Jill R; Horvath Sandor; Haraszti Laszlo; Majtenyi Katalin; Molnar Maria J; Budka Herbert; Ghetti Bernardino; Spina Salvatore
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.
Movement disorders : official journal of the Movement Disorder Society 2009;24(12):1843-7.
2009: Ghetti Bernardino
Old age before cognitive impairment.
Current Alzheimer research 2009;6(4):323.
2009: Ory-Magne Fabienne; Brefel-Courbon Christine; Payoux Pierre; Debruxelles Sabrina; Sibon Igor; Goizet Cyril; Labauge Pierre; Menegon Patrice; Uro-Coste Emmanuelle; Ghetti Bernardino; Delisle Marie Bernadetle; Vidal Ruben; Rascol Olivier
Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498-499InsTC).
Movement disorders : official journal of the Movement Disorder Society 2009;24(11):1676-83.
2009: Barbeito Ana G; Garringer Holly J; Baraibar Martin A; Gao Xiaoying; Arredondo Miguel; Núñez Marco T; Smith Mark A; Ghetti Bernardino; Vidal Ruben
Abnormal iron metabolism and oxidative stress in mice expressing a mutant form of the ferritin light polypeptide gene.
Journal of neurochemistry 2009;109(4):1067-78.
2009: Xiao Xiangzhu; Miravalle Leticia; Yuan Jue; McGeehan John; Dong Zhiqian; Wyza Robert; MacLennan Gregory T; Golichowski Alan M; Kneale Geoff; King Nicholas; Kong Qingzhong; Spina Salvatore; Vidal Ruben; Ghetti Bernardino; Roos Karen; Gambetti Pierluigi; Zou Wen-Quan
Failure to detect the presence of prions in the uterine and gestational tissues from a Gravida with Creutzfeldt-Jakob disease.
The American journal of pathology 2009;174(5):1602-8.
2009: 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; Tabaton Massimo
Mutant presenilin 1 increases the expression and activity of BACE1.
The Journal of biological chemistry 2009;284(14):9027-38.
2009: Mackenzie Ian R A; Neumann Manuela; Bigio Eileen H; Cairns Nigel J; Alafuzoff Irina; Kril Jillian; Kovacs Gabor G; Ghetti Bernardino; Halliday Glenda; Holm Ida E; Ince Paul G; Kamphorst Wouter; Revesz Tamas; Rozemuller Annemieke J M; Kumar-Singh Samir; Akiyama Haruhiko; Baborie Atik; Spina Salvatore; Dickson Dennis W; Trojanowski John Q; Mann David M A
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations.
Acta neuropathologica 2009;117(1):15-8.
2009: Vidal Ruben; Barbeito Ana G; Miravalle Leticia; Ghetti Bernardino
Cerebral amyloid angiopathy and parenchymal amyloid deposition in transgenic mice expressing the Danish mutant form of human BRI2.
Brain pathology (Zurich, Switzerland) 2009;19(1):58-68.
2009: Marti Joaquín; Santa-Cruz María C; Molina Vanessa; Serra Roger; Bayer Shirley A; Ghetti Bernardino; Hervás José P
Regional differences in the vulnerability of substantia nigra dopaminergic neurons in weaver mice.
Acta neurobiologiae experimentalis 2009;69(2):198-206.
2008: Chiesa Roberto; Piccardo Pedro; Biasini Emiliano; Ghetti Bernardino; Harris David A
Aggregated, wild-type prion protein causes neurological dysfunction and synaptic abnormalities.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2008;28(49):13258-67.
2008: Notari Silvio; Strammiello Rosaria; Capellari Sabina; Giese Armin; Cescatti Maura; Grassi Jacques; Ghetti Bernardino; Langeveld Jan P M; Zou Wen-Quan; Gambetti Pierluigi; Kretzschmar Hans A; Parchi Piero
Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease.
The Journal of biological chemistry 2008;283(45):30557-65.
2008: Kovacs Gabor G; Majtenyi Katalin; Spina Salvatore; Murrell Jill R; Gelpi Ellen; Hoftberger Romana; Fraser Graham; Crowther R Anthony; Goedert Michel; Budka Herbert; Ghetti Bernardino
White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration.
Journal of neuropathology and experimental neurology 2008;67(10):963-75.
2008: Van Vickle Gregory D; Esh Chera L; Kokjohn Tyler A; Patton R Lyle; Kalback Walter M; Luehrs Dean C; Beach Thomas G; Newel Amanda J; Lopera Francisco; Ghetti Bernardino; Vidal Ruben; Castaño Eduardo M; Roher Alex E
Presenilin-1 280Glu-->Ala mutation alters C-terminal APP processing yielding longer abeta peptides: implications for Alzheimer's disease.
Molecular medicine (Cambridge, Mass.) 2008;14(3-4):184-94.
2008: Velasco Ana; Fraser Graham; Delobel Patrice; Ghetti Bernardino; Lavenir Isabelle; Goedert Michel
Detection of filamentous tau inclusions by the fluorescent Congo red derivative FSB [(trans,trans)-1-fluoro-2,5-bis(3-hydroxycarbonyl-4-hydroxy)styrylbenzene].
FEBS letters 2008;582(6):901-6.
2008: Vidal Ruben; Miravalle Leticia; Gao Xiaoying; Barbeito Ana G; Baraibar Martin A; Hekmatyar Shahryar K; Widel Mario; Bansal Navin; Delisle Marie B; Ghetti Bernardino
Expression of a mutant form of the ferritin light chain gene induces neurodegeneration and iron overload in transgenic mice.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2008;28(1):60-7.
2008: Delobel Patrice; Lavenir Isabelle; Fraser Graham; Ingram Esther; Holzer Max; Ghetti Bernardino; Spillantini Maria Grazia; Crowther R Anthony; Goedert Michel
Analysis of tau phosphorylation and truncation in a mouse model of human tauopathy.
The American journal of pathology 2008;172(1):123-31.
2008: Spina Salvatore; Farlow Martin R; Unverzagt Frederick W; Kareken David A; Murrell Jill R; Fraser Graham; Epperson Francine; Crowther R Anthony; Spillantini Maria G; Goedert Michel; Ghetti Bernardino
The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family.
Brain : a journal of neurology 2008;131(Pt 1):72-89.
2008: Maarouf Chera L; Daugs Ian D; Spina Salvatore; Vidal Ruben; Kokjohn Tyler A; Patton R Lyle; Kalback Walter M; Luehrs Dean C; Walker Douglas G; Castaño Eduardo M; Beach Thomas G; Ghetti Bernardino; Roher Alex E
Histopathological and molecular heterogeneity among individuals with dementia associated with Presenilin mutations.
Molecular neurodegeneration 2008;3():20.
2008: Ghetti Bernardino; Spina Salvatore; Murrell Jill R; Huey Edward D; Pietrini Pietro; Sweeney Brian; Wassermann Eric M; Keohane Catherine; Farlow Martin R; Grafman Jordan
In vivo and postmortem clinicoanatomical correlations in frontotemporal dementia and parkinsonism linked to chromosome 17.
Neuro-degenerative diseases 2008;5(3-4):215-7.
2007: Martí Joaquín; Santa-Cruz M C; Bayer Shirley A; Ghetti Bernardino; Hervás José P
Purkinje cell age-distribution in fissures and in foliar crowns: a comparative study in the weaver cerebellum.
Brain structure & function 2007;212(3-4):347-57.
2007: Ingelsson Martin; Ramasamy Karunya; Russ Carsten; Freeman Stefanie H; Orne Jennifer; Raju Susan; Matsui Toshifumi; Growdon John H; Frosch Matthew P; Ghetti Bernardino; Brown Robert H; Irizarry Michael C; Hyman Bradley T
Increase in the relative expression of tau with four microtubule binding repeat regions in frontotemporal lobar degeneration and progressive supranuclear palsy brains.
Acta neuropathologica 2007;114(5):471-9.
2007: Spina Salvatore; Murrell Jill R; Huey Edward D; Wassermann Eric M; Pietrini Pietro; Grafman Jordan; Ghetti Bernardino
Corticobasal syndrome associated with the A9D Progranulin mutation.
Journal of neuropathology and experimental neurology 2007;66(10):892-900.
2007: Rademakers Rosa; Baker Matt; Gass Jennifer; Adamson Jennifer; Huey Edward D; Momeni Parastoo; Spina Salvatore; Coppola Giovanni; Karydas Anna M; Stewart Heather; Johnson Nancy; Hsiung Ging-Yuek; Kelley Brendan; Kuntz Karen; Steinbart Ellen; Wood Elisabeth McCarty; Yu Chang-En; Josephs Keith; Sorenson Eric; Womack Kyle B; Weintraub Sandra; Pickering-Brown Stuart M; Schofield Peter R; Brooks William S; Van Deerlin Vivianna M; Snowden Julie; Clark Christopher M; Kertesz Andrew; Boylan Kevin; Ghetti Bernardino; Neary David; Schellenberg Gerard D; Beach Thomas G; Mesulam Marsel; Mann David; Grafman Jordan; Mackenzie Ian R; Feldman Howard; Bird Thomas; Petersen Ron; Knopman David; Boeve Bradley; Geschwind Dan H; Miller Bruce; Wszolek Zbigniew; Lippa Carol; Bigio Eileen H; Dickson Dennis; Graff-Radford Neill; Hutton Mike
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.
Lancet neurology 2007;6(10):857-68.
2007: Filley Christopher M; Rollins Yvonne D; Anderson C Alan; Arciniegas David B; Howard Katherine L; Murrell Jill R; Boyer Philip J; Kleinschmidt-DeMasters Belte K; Ghetti Bernardino
The genetics of very early onset Alzheimer disease.
Cognitive and behavioral neurology : official journal of the Society for Behavioral and Cognitive Neurology 2007;20(3):149-56.
2007: Martí Joaquín; Santa-Cruz M C; Bayer Shirley A; Ghetti Bernardino; Hervás José P
Generation and survival of midbrain dopaminergic neurons in weaver mice.
International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 2007;25(5):299-307.
2007: 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
Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation.
Journal of neural transmission (Vienna, Austria : 1996) 2007;114(7):947-50.
2007: Li Aimin; Piccardo Pedro; Barmada Sami J; Ghetti Bernardino; Harris David A
Prion protein with an octapeptide insertion has impaired neuroprotective activity in transgenic mice.
The EMBO journal 2007;26(11):2777-85.
2007: Piccini Alessandra; Zanusso Gianluigi; Borghi Roberta; Noviello Cristiana; Monaco Salvatore; Russo Roberta; Damonte Gianluca; Armirotti Andrea; Gelati Matteo; Giordano Renzo; Zambenedetti Pamela; Russo Claudio; Ghetti Bernardino; Tabaton Massimo
Association of a presenilin 1 S170F mutation with a novel Alzheimer disease molecular phenotype.
Archives of neurology 2007;64(5):738-45.
2007: Spina Salvatore; Murrell Jill R; Yoshida Hirotaka; Ghetti Bernardino; Bermingham Niamh; Sweeney Brian; Dlouhy Stephen R; Crowther R Anthony; Goedert Michel; Keohane Catherine
The novel Tau mutation G335S: clinical, neuropathological and molecular characterization.
Acta neuropathologica 2007;113(4):461-70.
2007: Ringman John M; Rodriguez Yaneth; Diaz-Olavarrieta Claudia; Chavez Mireya; Thompson Michael; Fairbanks Lynn; Paz Francisco; Varpetian Arousiak; Chaparro Hector; Macias-Islas Miguel Angel; Murrell Jill; Ghetti Bernardino; Kawas Claudia
Performance on MMSE sub-items and education level in presenilin-1 mutation carriers without dementia.
International psychogeriatrics / IPA 2007;19(2):323-32.
2007: Piccardo Pedro; Manson Jean C; King Declan; Ghetti Bernardino; Barron Rona M
Accumulation of prion protein in the brain that is not associated with transmissible disease.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(11):4712-7.
2007: Spina S; Murrell J R; Huey E D; Wassermann E M; Pietrini P; Baraibar M A; Barbeito A G; Troncoso J C; Vidal R; Ghetti B; Grafman J
Clinicopathologic features of frontotemporal dementia with progranulin sequence variation.
Neurology 2007;68(11):820-7.
2007: Di Fede Giuseppe; Giaccone Giorgio; Limido Lucia; Mangieri Michela; Suardi Silvia; Puoti Gianfranco; Morbin Michela; Mazzoleni Giulia; Ghetti Bernardino; Tagliavini Fabrizio
The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease.
Journal of neuropathology and experimental neurology 2007;66(2):124-30.
2007: Goedert Michel; Ghetti Bernardino
Alois Alzheimer: his life and times.
Brain pathology (Zurich, Switzerland) 2007;17(1):57-62.
2006: Murrell Jill; Ghetti Bernardino; Cochran Elizabeth; Macias-Islas Miguel Angel; Medina Luis; Varpetian Arousiak; Cummings Jeffrey L; Mendez Mario F; Kawas Claudia; Chui Helena; Ringman John M
The A431E mutation in PSEN1 causing familial Alzheimer's disease originating in Jalisco State, Mexico: an additional fifteen families.
Neurogenetics 2006;7(4):277-9.
2006: Huey Edward D; Grafman Jordan; Wassermann Eric M; Pietrini Pietro; Tierney Michael C; Ghetti Bernardino; Spina Salvatore; Baker Matt; Hutton Mike; Elder Joshua W; Berger Stephen L; Heflin Kyle A; Hardy John; Momeni Parastoo
Characteristics of frontotemporal dementia patients with a Progranulin mutation.
Annals of neurology 2006;60(3):374-80.
2006: Radde Rebecca; Bolmont Tristan; Kaeser Stephan A; Coomaraswamy Janaky; Lindau Dennis; Stoltze Lars; Calhoun Michael E; Jäggi Fabienne; Wolburg Hartwig; Gengler Simon; Haass Christian; Ghetti Bernardino; Czech Christian; Hölscher Christian; Mathews Paul M; Jucker Mathias
Abeta42-driven cerebral amyloidosis in transgenic mice reveals early and robust pathology.
EMBO reports 2006;7(9):940-6.
2006: Schweitzer Kelly; Decker Emily; Zhu Liping; Miller Richard E; Mirra Suzanne S; Spina Salvatore; Ghetti Bernardino; Wang Mu; Murrell Jill
Aberrantly regulated proteins in frontotemporal dementia.
Biochemical and biophysical research communications 2006;348(2):465-72.
2006: Moroncini Gianluca; Mangieri Michela; Morbin Michela; Mazzoleni Giulia; Ghetti Bernardino; Gabrielli Armando; Williamson Robert Anthony; Giaccone Giorgio; Tagliavini Fabrizio
Pathologic prion protein is specifically recognized in situ by a novel PrP conformational antibody.
Neurobiology of disease 2006;23(3):717-24.
2006: Ghetti Bernardino; Goebel Hans H
Frontotemporal dementia: the post-tau era.
Neurology 2006;67(4):560-1.
2006: Shiarli A-M; Jennings R; Shi J; Bailey K; Davidson Y; Tian J; Bigio E H; Ghetti B; Murrell J R; Delisle M B; Mirra S; Crain B; Zolo P; Arima K; Iseki E; Murayama S; Kretzschmar H; Neumann M; Lippa C; Halliday G; Mackenzie J; Khan N; Ravid R; Dickson D; Wszolek Z; Iwatsubo T; Pickering-Brown S M; Mann D M A
Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease.
Neuropathology and applied neurobiology 2006;32(4):374-87.
2006: Colucci Monica; Moleres Francisco J; Xie Zhi-Liang; Ray-Chaudhury Abhik; Gutti Sujata; Butefisch Cathrin M; Cervenakova Larisa; Wang Wen; Goldfarb Lev G; Kong Qingzhong; Ghetti Bernardino; Chen Shu G; Gambetti Pierluigi
Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP deposits.
Journal of neuropathology and experimental neurology 2006;65(7):642-51.
2006: Tofaris George K; Garcia Reitböck Pablo; Humby Trevor; Lambourne Sarah L; O'Connell Mark; Ghetti Bernardino; Gossage Helen; Emson Piers C; Wilkinson Lawrence S; Goedert Michel; Spillantini Maria Grazia
Pathological changes in dopaminergic nerve cells of the substantia nigra and olfactory bulb in mice transgenic for truncated human alpha-synuclein(1-120): implications for Lewy body disorders.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2006;26(15):3942-50.
2006: Baba Yasuhiko; Ghetti Bernardino; Baker Matthew C; Uitti Ryan J; Hutton Michael L; Yamaguchi Keiji; Bird Thomas; Lin Wenlang; DeLucia Michael W; Dickson Dennis W; Wszolek Zbigniew K
Hereditary diffuse leukoencephalopathy with spheroids: clinical, pathologic and genetic studies of a new kindred.
Acta neuropathologica 2006;111(4):300-11.
2006: Delobel Patrice; Lavenir Isabelle; Ghetti Bernardino; Holzer Max; Goedert Michel
Cell-cycle markers in a transgenic mouse model of human tauopathy: increased levels of cyclin-dependent kinase inhibitors p21Cip1 and p27Kip1.
The American journal of pathology 2006;168(3):878-87.
2006: Ghetti Bernardino
Neurodegeneration and hereditary dementias: 40 years of learning.
Journal of Alzheimer's disease : JAD 2006;9(3 Suppl):45-52.
2006: Spillantini Maria Grazia; Murrell Jill R; Goedert Michel; Farlow Martin; Klug Aaron; Ghetti Bernardino
Mutations in the tau gene (MAPT) in FTDP-17: the family with Multiple System Tauopathy with Presenile Dementia (MSTD).
Journal of Alzheimer's disease : JAD 2006;9(3 Suppl):373-80.
2006: Wszolek Zbigniew K; Tsuboi Yoshio; Ghetti Bernardino; Pickering-Brown Stuart; Baba Yasuhiko; Cheshire William P
Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).
Orphanet journal of rare diseases 2006;1():30.
2005: Castellani Rudy J; Siedlak Sandra L; Fortino Anne E; Perry George; Ghetti Bernardino; Smith Mark A
Chitin-like polysaccharides in Alzheimer's disease brains.
Current Alzheimer research 2005;2(4):419-23.
2005: Esh Chera; Patton Lyle; Kalback Walter; Kokjohn Tyler A; Lopez John; Brune Daniel; Newell Amanda J; Beach Thomas; Schenk Dale; Games Dora; Paul Steven; Bales Kelly; Ghetti Bernardino; Castaño Eduardo M; Roher Alex E
Altered APP processing in PDAPP (Val717 --> Phe) transgenic mice yields extended-length Abeta peptides.
Biochemistry 2005;44(42):13807-19.
2005: Petersen Robert B; Siedlak Sandra L; Lee Hyoung-gon; Kim Yong-Sun; Nunomura Akihiko; Tagliavini Fabrizio; Ghetti Bernardino; Cras Patrick; Moreira Paula I; Castellani Rudy J; Guentchev Marin; Budka Herbert; Ironside James W; Gambetti Pierluigi; Smith Mark A; Perry George
Redox metals and oxidative abnormalities in human prion diseases.
Acta neuropathologica 2005;110(3):232-8.
2005: Yamaguchi Keiji; Cochran Elizabeth J; Murrell Jill R; Polymeropoulos Mihael H; Shannon Kathleen M; Crowther R Anthony; Goedert Michel; Ghetti Bernardino
Abundant neuritic inclusions and microvacuolar changes in a case of diffuse Lewy body disease with the A53T mutation in the alpha-synuclein gene.
Acta neuropathologica 2005;110(3):298-305.
2005: Ringman J M; Diaz-Olavarrieta C; Rodriguez Y; Chavez M; Fairbanks L; Paz F; Varpetian A; Maldonado H C; Macias-Islas M A; Murrell J; Ghetti B; Kawas C
Neuropsychological function in nondemented carriers of presenilin-1 mutations.
Neurology 2005;65(4):552-8.
2005: Miravalle Leticia; Calero Miguel; Takao Masaki; Roher Alex E; Ghetti Bernardino; Vidal Ruben
Amino-terminally truncated Abeta peptide species are the main component of cotton wool plaques.
Biochemistry 2005;44(32):10810-21.
2005: Ghetti Bernardino
Recognition: robert terry.
Alzheimer's & dementia : the journal of the Alzheimer's Association 2005;1(1):78.
2005: Baba Yasuhiko; Tsuboi Yoshio; Baker Matthew C; Uitti Ryan J; Hutton Michael L; Dickson Dennis W; Farrer Matthew; Putzke John D; Woodruff Bryan K; Ghetti Bernardino; Murrell Jill R; Boeve Bradley F; Petersen Ronald C; Verpillat Patrice; Brice Alexis; Delisle Marie-Bernadette; Rascol Oliver; Arima Kunimasa; Dysken Maurice W; Yasuda Minoru; Kobayashi Tomonori; Sunohara Nobuhiko; Komure Osamu; Kuno Sadako; Sperfeld Anne D; Stoppe Gabriela; Kohlhase Jürgen; Pickering-Brown Stuart; Neary David; Bugiani Orso; Wszolek Zbigniew K
The effect of tau genotype on clinical features in FTDP-17.
Parkinsonism & related disorders 2005;11(4):205-8.
2005: Zaidi Syed I A; Richardson Sandra L; Capellari Sabina; Song Li; Smith Mark A; Ghetti Bernardino; Sy Man-Sun; Gambetti Pierluigi; Petersen Robert B
Characterization of the F198S prion protein mutation: enhanced glycosylation and defective refolding.
Journal of Alzheimer's disease : JAD 2005;7(2):159-71; discussion 173-80.
2005: Boeve Bradley F; Tremont-Lukats Ivo W; Waclawik Andrew J; Murrell Jill R; Hermann Bruce; Jack Clifford R; Shiung Maria M; Smith Glenn E; Nair Anil R; Lindor Noralane; Koppikar Vinaya; Ghetti Bernardino
Longitudinal characterization of two siblings with frontotemporal dementia and parkinsonism linked to chromosome 17 associated with the S305N tau mutation.
Brain : a journal of neurology 2005;128(Pt 4):752-72.
2005: Stewart Richard S; Piccardo Pedro; Ghetti Bernardino; Harris David A
Neurodegenerative illness in transgenic mice expressing a transmembrane form of the prion protein.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2005;25(13):3469-77.
2005: Gemignani A; Pietrini P; Murrell J R; Glazier B S; Zolo P; Guazzelli M; Ghetti B
Slow wave and rem sleep mechanisms are differently altered in hereditary pick disease associated with the TAU G389R mutation.
Archives italiennes de biologie 2005;143(1):65-79.
2005: Chiesa Roberto; Piccardo Pedro; Dossena Sara; Nowoslawski Lisa; Roth Kevin A; Ghetti Bernardino; Harris David A
Bax deletion prevents neuronal loss but not neurological symptoms in a transgenic model of inherited prion disease.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(1):238-43.
2004: Vidal Ruben; Delisle Marie Bernadette; Ghetti Bernardino
Neurodegeneration caused by proteins with an aberrant carboxyl-terminus.
Journal of neuropathology and experimental neurology 2004;63(8):787-800.
2004: Woodruff Bryan K; Baba Yasuhiko; Hutton Michael L; Wszolek Zbigniew K; Tsuboi Yoshio; Kobayashi Tomonori; Ghetti Bernardino; Arima Kunimasa; Yasuda Minoru; Rascol Olivier
Haplotype-phenotype correlations in kindreds with the N279K mutation in the tau gene.
Archives of neurology 2004;61(8):1327; author reply 1327.
2004: Barmada Sami; Piccardo Pedro; Yamaguchi Keiji; Ghetti Bernardino; Harris David A
GFP-tagged prion protein is correctly localized and functionally active in the brains of transgenic mice.
Neurobiology of disease 2004;16(3):527-37.
2004: Takao Masaki; Ghetti Bernardino; Yoshida Hirotaka; Piccardo Pedro; Narain Yolanda; Murrell Jill R; Vidal Ruben; Glazier Bradley S; Jakes Ross; Tsutsui Miho; Spillantini Maria Grazia; Crowther R Anthony; Goedert Michel; Koto Atsuo
Early-onset dementia with Lewy bodies.
Brain pathology (Zurich, Switzerland) 2004;14(2):137-47.
2004: Vidal R; Ghetti B; Takao M; Brefel-Courbon C; Uro-Coste E; Glazier B S; Siani V; Benson M D; Calvas P; Miravalle L; Rascol O; Delisle M B
Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide gene.
Journal of neuropathology and experimental neurology 2004;63(4):363-80.
2004: Notari Silvio; Capellari Sabina; Giese Armin; Westner Ingo; Baruzzi Agostino; Ghetti Bernardino; Gambetti Pierluigi; Kretzschmar Hans A; Parchi Piero
Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJD.
The Journal of biological chemistry 2004;279(16):16797-804.
2004: Vitali Antonella; Piccini Alessandra; Borghi Roberta; Fornaro Pantaleo; Siedlak Sandra L; Smith Mark A; Gambetti Pierluigi; Ghetti Bernardino; Tabaton Massimo
Soluble amyloid beta-protein is increased in frontotemporal dementia with tau gene mutations.
Journal of Alzheimer's disease : JAD 2004;6(1):45-51.
2004: Roher Alex E; Kokjohn Tyler A; Esh Chera; Weiss Nicole; Childress Jennifer; Kalback Walter; Luehrs Dean C; Lopez John; Brune Daniel; Kuo Yu-Min; Farlow Martin; Murrell Jill; Vidal Ruben; Ghetti Bernardino
The human amyloid-beta precursor protein770 mutation V717F generates peptides longer than amyloid-beta-(40-42) and flocculent amyloid aggregates.
The Journal of biological chemistry 2004;279(7):5829-36.
2003: Tofaris George K; Razzaq Azam; Ghetti Bernardino; Lilley Kathryn S; Spillantini Maria Grazia
Ubiquitination of alpha-synuclein in Lewy bodies is a pathological event not associated with impairment of proteasome function.
The Journal of biological chemistry 2003;278(45):44405-11.
2003: De Michele Giuseppe; Pocchiari Maurizio; Petraroli Rossella; Manfredi Mario; Caneve Giorgio; Coppola Giovanni; Casali Carlo; Saccà Francesco; Piccardo Pedro; Salvatore Elena; Berardelli Alfredo; Orio Marcello; Barbieri Fabrizio; Ghetti Bernardino; Filla Alessandro
Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2003;30(3):233-6.
2003: Powers J M; Byrne N P; Ito M; Takao M; Yankopoulou D; Spillantini M G; Ghetti B
A novel leukoencephalopathy associated with tau deposits primarily in white matter glia.
Acta neuropathologica 2003;106(2):181-7.
2003: Chiesa Roberto; Piccardo Pedro; Quaglio Elena; Drisaldi Bettina; Si-Hoe San Ling; Takao Masaki; Ghetti Bernardino; Harris David A
Molecular distinction between pathogenic and infectious properties of the prion protein.
Journal of virology 2003;77(13):7611-22.
2003: Harris David A; Chiesa Roberto; Drisaldi Bettina; Quaglio Elena; Migheli Antonio; Piccardo Pedro; Ghetti Bernardino
A murine model of a familial prion disease.
Clinics in laboratory medicine 2003;23(1):175-86.
2003: Ghetti Bernardino; Tagliavini Fabrizio; Takao M; Bugiani Orso; Piccardo Pedro
Hereditary prion protein amyloidoses.
Clinics in laboratory medicine 2003;23(1):65-85, viii.
2003: Vidal Ruben; Delisle Marie Bernadette; Rascol Olivier; Ghetti Bernardino
Hereditary ferritinopathy.
Journal of the neurological sciences 2003;207(1-2):110-1.
2002: Tsuboi Y; Baker M; Hutton M L; Uitti R J; Rascol O; Delisle M-B; Soulages X; Murrell J R; Ghetti B; Yasuda M; Komure O; Kuno S; Arima K; Sunohara N; Kobayashi T; Mizuno Y; Wszolek Z K
Clinical and genetic studies of families with the tau N279K mutation (FTDP-17).
Neurology 2002;59(11):1791-3.
2002: Allen Bridget; Ingram Esther; Takao Masaki; Smith Michael J; Jakes Ross; Virdee Kanwar; Yoshida Hirotaka; Holzer Max; Craxton Molly; Emson Piers C; Atzori Cristiana; Migheli Antonio; Crowther R Anthony; Ghetti Bernardino; Spillantini Maria Grazia; Goedert Michel
Abundant tau filaments and nonapoptotic neurodegeneration in transgenic mice expressing human P301S tau protein.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2002;22(21):9340-51.
2002: Zhong Jin; Deng Jixian; Ghetti Bernardino; Lee Wei-Hua
Inhibition of insulin-like growth factor I activity contributes to the premature apoptosis of cerebellar granule neuron in weaver mutant mice: in vitro analysis.
Journal of neuroscience research 2002;70(1):36-45.
2002: Adamec Emil; Murrell Jill R; Takao Masaki; Hobbs Wendy; Nixon Ralph A; Ghetti Bernardino; Vonsattel Jean P
P301L tauopathy: confocal immunofluorescence study of perinuclear aggregation of the mutated protein.
Journal of the neurological sciences 2002;200(1-2):85-93.
2002: Takao Masaki; Ghetti Bernardino; Hayakawa Isao; Ikeda Eiji; Fukuuchi Yasuo; Miravalle Leticia; Piccardo Pedro; Murrell Jill R; Glazier Bradley S; Koto Atsuo
A novel mutation (G217D) in the Presenilin 1 gene ( PSEN1) in a Japanese family: presenile dementia and parkinsonism are associated with cotton wool plaques in the cortex and striatum.
Acta neuropathologica 2002;104(2):155-70.
2002: Ogunnyi Adesola; Akang Effiong E U; Gureje Oye; Takao Masaki; Piccardo Pedro; Baiyewu Olusegun; Hall Kathleen S; Ghetti Bernardino; Hendrie Hugh C
Dementia with Lewy bodies in a Nigerian: a case report.
International psychogeriatrics / IPA 2002;14(2):211-8.
2002: Martí Joaquín; Wills Katherine V; Ghetti Bernardino; Bayer Shirley A
A combined immunohistochemical and autoradiographic method to detect midbrain dopaminergic neurons and determine their time of origin.
Brain research. Brain research protocols 2002;9(3):197-205.
2002: Davis Richard L; Shrimpton Antony E; Carrell Robin W; Lomas David A; Gerhard Lieselotte; Baumann Bruno; Lawrence Daniel A; Yepes Manuel; Kim Tai Seung; Ghetti Bernardino; Piccardo Pedro; Takao Masaki; Lacbawan Felicitas; Muenke Maximilian; Sifers Richard N; Bradshaw Charles B; Kent Paul F; Collins George H; Larocca Daria; Holohan Peter D
Association between conformational mutations in neuroserpin and onset and severity of dementia.
Lancet 2002;359(9325):2242-7.
2002: Tsuboi Yoshio; Uitti Ryan J; Delisle Marie-Bernadette; Ferreira Joaquim J; Brefel-Courbon Christine; Rascol Olivier; Ghetti Bernardino; Murrell Jill R; Hutton Michael; Baker Matthew; Wszolek Zbigniew K
Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: a comparison of the pallidopontonigral degeneration kindred and a French family.
Archives of neurology 2002;59(6):943-50.
2002: Moehlmann Tobias; Winkler Edith; Xia Xuefeng; Edbauer Dieter; Murrell Jill; Capell Anja; Kaether Christoph; Zheng Hui; Ghetti Bernardino; Haass Christian; Steiner Harald
Presenilin-1 mutations of leucine 166 equally affect the generation of the Notch and APP intracellular domains independent of their effect on Abeta 42 production.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(12):8025-30.
2002: Marti Joaquin; Wills Katherine V; Ghetti Bernardino; Bayer Shirley A
Regional differences in the Purkinje cells settled pattern: a comparative autoradiographic study in control and homozygous weaver mice.
Experimental neurology 2002;175(1):168-81.
2002: Taratuto Ana Lia; Piccardo P; Reich E G; Chen S G; Sevlever G; Schultz M; Luzzi A A; Rugiero M; Abecasis G; Endelman M; Garcia A M; Capellari S; Xie Z; Lugaresi E; Gambetti P; Dlouhy S R; Ghetti B
Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease.
Neurology 2002;58(3):362-7.
2001: Atzori C; Ghetti B; Piva R; Srinivasan A N; Zolo P; Delisle M B; Mirra S S; Migheli A
Activation of the JNK/p38 pathway occurs in diseases characterized by tau protein pathology and is related to tau phosphorylation but not to apoptosis.
Journal of neuropathology and experimental neurology 2001;60(12):1190-7.
2001: Takao M; Ghetti B; Murrell J R; Unverzagt F W; Giaccone G; Tagliavini F; Bugiani O; Piccardo P; Hulette C M; Crain B J; Farlow M R; Heyman A
Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizures.
Journal of neuropathology and experimental neurology 2001;60(12):1137-52.
2001: Panegyres P K; Toufexis K; Kakulas B A; Cernevakova L; Brown P; Ghetti B; Piccardo P; Dlouhy S R
A new PRNP mutation (G131V) associated with Gerstmann-Sträussler-Scheinker disease.
Archives of neurology 2001;58(11):1899-902.
2001: Martí J; Wills K V; Ghetti B; Bayer S A
Evidence that the loss of Purkinje cells and deep cerebellar nuclei neurons in homozygous weaver is not related to neurogenetic patterns.
International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 2001;19(6):599-610.
2001: Piccardo P; Liepnieks J J; William A; Dlouhy S R; Farlow M R; Young K; Nochlin D; Bird T D; Nixon R R; Ball M J; DeCarli C; Bugiani O; Tagliavini F; Benson M D; Ghetti B
Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations.
The American journal of pathology 2001;158(6):2201-7.
2001: Chiesa R; Pestronk A; Schmidt R E; Tourtellotte W G; Ghetti B; Piccardo P; Harris D A
Primary myopathy and accumulation of PrPSc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutation.
Neurobiology of disease 2001;8(2):279-88.
2001: Tagliavini F; Lievens P M; Tranchant C; Warter J M; Mohr M; Giaccone G; Perini F; Rossi G; Salmona M; Piccardo P; Ghetti B; Beavis R C; Bugiani O; Frangione B; Prelli F
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.
The Journal of biological chemistry 2001;276(8):6009-15.
2001: Levy E; Sastre M; Kumar A; Gallo G; Piccardo P; Ghetti B; Tagliavini F
Codeposition of cystatin C with amyloid-beta protein in the brain of Alzheimer disease patients.
Journal of neuropathology and experimental neurology 2001;60(1):94-104.
2001: Yazaki M; Liepnieks J J; Murrell J R; Takao M; Guenther B; Piccardo P; Farlow M R; Ghetti B; Benson M D
Biochemical characterization of a neuroserpin variant associated with hereditary dementia.
The American journal of pathology 2001;158(1):227-33.
2000: Takao M; Benson M D; Murrell J R; Yazaki M; Piccardo P; Unverzagt F W; Davis R L; Holohan P D; Lawrence D A; Richardson R; Farlow M R; Ghetti B
Neuroserpin mutation S52R causes neuroserpin accumulation in neurons and is associated with progressive myoclonus epilepsy.
Journal of neuropathology and experimental neurology 2000;59(12):1070-86.
2000: Lippa C F; Swearer J M; Kane K J; Nochlin D; Bird T D; Ghetti B; Nee L E; St George-Hyslop P; Pollen D A; Drachman D A
Familial Alzheimer's disease: site of mutation influences clinical phenotype.
Annals of neurology 2000;48(3):376-9.
2000: Parchi P; Zou W; Wang W; Brown P; Capellari S; Ghetti B; Kopp N; Schulz-Schaeffer W J; Kretzschmar H A; Head M W; Ironside J W; Gambetti P; Chen S G
Genetic influence on the structural variations of the abnormal prion protein.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(18):10168-72.
2000: Martí J; Wills K V; Ghetti B; Bayer S A
The weaver gene continues to target late-generated dopaminergic neurons in midbrain areas at P90.
Brain research. Developmental brain research 2000;122(2):173-81.
2000: Martí J; Wills K V; Ghetti B; Bayer S A
The weaver gene has no effect on the generation patterns of mesencephalic dopaminergic neurons.
Brain research. Developmental brain research 2000;122(2):165-72.
2000: Vidal R; Calero M; Piccardo P; Farlow M R; Unverzagt F W; Méndez E; Jiménez-Huete A; Beavis R; Gallo G; Gomez-Tortosa E; Ghiso J; Hyman B T; Frangione B; Ghetti B
Senile dementia associated with amyloid beta protein angiopathy and tau perivascular pathology but not neuritic plaques in patients homozygous for the APOE-epsilon4 allele.
Acta neuropathologica 2000;100(1):1-12.
2000: Bugiani O; Giaccone G; Piccardo P; Morbin M; Tagliavini F; Ghetti B
Neuropathology of Gerstmann-Sträussler-Scheinker disease.
Microscopy research and technique 2000;50(1):10-5.
2000: Murrell J R; Hake A M; Quaid K A; Farlow M R; Ghetti B
Early-onset Alzheimer disease caused by a new mutation (V717L) in the amyloid precursor protein gene.
Archives of neurology 2000;57(6):885-7.
2000: Russo C; Schettini G; Saido T C; Hulette C; Lippa C; Lannfelt L; Ghetti B; Gambetti P; Tabaton M; Teller J K
Presenilin-1 mutations in Alzheimer's disease.
Nature 2000;405(6786):531-2.
2000: Chiesa R; Drisaldi B; Quaglio E; Migheli A; Piccardo P; Ghetti B; Harris D A
Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(10):5574-9.
2000: Harkins A B; Dlouhy S; Ghetti B; Cahill A L; Won L; Heller B; Heller A; Fox A P
Evidence of elevated intracellular calcium levels in weaver homozygote mice.
The Journal of physiology 2000;524 Pt 2():447-55.
2000: Harris D A; Chiesa R; Drisaldi B; Quaglio E; Migheli A; Piccardo P; Ghetti B
A transgenic model of a familial prion disease.
Archives of virology. Supplementum 2000;(16):103-12.
2000: Goedert M; Ghetti B; Spillantini M G
Tau gene mutations in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). Their relevance for understanding the neurogenerative process.
Annals of the New York Academy of Sciences 2000;920():74-83.
2000: Ghetti B; Murrell J R; Zolo P; Spillantini M G; Goedert M
Progress in hereditary tauopathies: a mutation in the Tau gene (G389R) causes a Pick disease-like syndrome.
Annals of the New York Academy of Sciences 2000;920():52-62.
2000: Delisle M B; Uro-Coste E; Murrell J R; Rascol O; Ghetti B
[Neurodegenerative disease associated with a mutation of codon 279 (N279K) in exon 10 of Tau protein]
Bulletin de l'Académie nationale de médecine 2000;184(4):799-809; discussion 809-11.
1999: Bales K R; Verina T; Cummins D J; Du Y; Dodel R C; Saura J; Fishman C E; DeLong C A; Piccardo P; Petegnief V; Ghetti B; Paul S M
Apolipoprotein E is essential for amyloid deposition in the APP(V717F) transgenic mouse model of Alzheimer's disease.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(26):15233-8.
1999: Murrell J R; Spillantini M G; Zolo P; Guazzelli M; Smith M J; Hasegawa M; Redi F; Crowther R A; Pietrini P; Ghetti B; Goedert M
Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits.
Journal of neuropathology and experimental neurology 1999;58(12):1207-26.
1999: Ghetti B; Murrell J; Spillantini M G
Mutations in the Tau gene cause frontotemporal dementia.
Brain research bulletin 1999;50(5-6):471-2.
1999: Zhang W; Ghetti B; Yang X L; Lee W
Alteration of IGF system gene expression during the postnatal development of pcd mice.
The Journal of endocrinology 1999;163(2):191-8.
1999: Broome J D; Wills K V; Lapchak P A; Ghetti B; Camp L L; Bayer S A
Glial cell line-derived neurotrophic factor protects midbrain dopamine neurons from the lethal action of the weaver gene: a quantitative immunocytochemical study.
Brain research. Developmental brain research 1999;116(1):1-7.
1999: Parchi P; Giese A; Capellari S; Brown P; Schulz-Schaeffer W; Windl O; Zerr I; Budka H; Kopp N; Piccardo P; Poser S; Rojiani A; Streichemberger N; Julien J; Vital C; Ghetti B; Gambetti P; Kretzschmar H
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.
Annals of neurology 1999;46(2):224-33.
1999: Migheli A; Piva R; Casolino S; Atzori C; Dlouhy S R; Ghetti B
A cell cycle alteration precedes apoptosis of granule cell precursors in the weaver mouse cerebellum.
The American journal of pathology 1999;155(2):365-73.
1999: Delisle M B; Murrell J R; Richardson R; Trofatter J A; Rascol O; Soulages X; Mohr M; Calvas P; Ghetti B
A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy.
Acta neuropathologica 1999;98(1):62-77.
1999: Varani L; Hasegawa M; Spillantini M G; Smith M J; Murrell J R; Ghetti B; Klug A; Goedert M; Varani G
Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(14):8229-34.
1999: Bugiani O; Murrell J R; Giaccone G; Hasegawa M; Ghigo G; Tabaton M; Morbin M; Primavera A; Carella F; Solaro C; Grisoli M; Savoiardo M; Spillantini M G; Tagliavini F; Goedert M; Ghetti B
Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau.
Journal of neuropathology and experimental neurology 1999;58(6):667-77.
1999: Mirra S S; Murrell J R; Gearing M; Spillantini M G; Goedert M; Crowther R A; Levey A I; Jones R; Green J; Shoffner J M; Wainer B H; Schmidt M L; Trojanowski J Q; Ghetti B
Tau pathology in a family with dementia and a P301L mutation in tau.
Journal of neuropathology and experimental neurology 1999;58(4):335-45.
1998: Chiesa R; Piccardo P; Ghetti B; Harris D A
Neurological illness in transgenic mice expressing a prion protein with an insertional mutation.
Neuron 1998;21(6):1339-51.
1998: Schwartz N B; Szabo M; Verina T; Wei J; Dlouhy S R; Won L; Heller A; Hodes M E; Ghetti B
Hypothalamic-pituitary-gonadal axis in the mutant weaver mouse.
Neuroendocrinology 1998;68(6):374-85.
1998: Fox A P; Dlouhy S; Ghetti B; Hurley J H; Nucifora P G; Nelson D J; Won L; Heller A
Altered responses to potassium in cerebellar neurons from weaver heterozygote mice.
Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale 1998;123(3):298-306.
1998: Jiménez-Huete A; Lievens P M; Vidal R; Piccardo P; Ghetti B; Tagliavini F; Frangione B; Prelli F
Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissues.
The American journal of pathology 1998;153(5):1561-72.
1998: Lippa C F; Fujiwara H; Mann D M; Giasson B; Baba M; Schmidt M L; Nee L E; O'Connell B; Pollen D A; St George-Hyslop P; Ghetti B; Nochlin D; Bird T D; Cairns N J; Lee V M; Iwatsubo T; Trojanowski J Q
Lewy bodies contain altered alpha-synuclein in brains of many familial Alzheimer's disease patients with mutations in presenilin and amyloid precursor protein genes.
The American journal of pathology 1998;153(5):1365-70.
1998: Piccardo P; Dlouhy S R; Lievens P M; Young K; Bird T D; Nochlin D; Dickson D W; Vinters H V; Zimmerman T R; Mackenzie I R; Kish S J; Ang L C; De Carli C; Pocchiari M; Brown P; Gibbs C J; Gajdusek D C; Bugiani O; Ironside J; Tagliavini F; Ghetti B
Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity.
Journal of neuropathology and experimental neurology 1998;57(10):979-88.
1998: Wei J; Hodes M E; Piva R; Feng Y; Wang Y; Ghetti B; Dlouhy S R
Characterization of murine Girk2 transcript isoforms: structure and differential expression.
Genomics 1998;51(3):379-90.
1998: Spillantini M G; Murrell J R; Goedert M; Farlow M R; Klug A; Ghetti B
Mutation in the tau gene in familial multiple system tauopathy with presenile dementia.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(13):7737-41.
1998: Piccardo P; Langeveld J P; Hill A F; Dlouhy S R; Young K; Giaccone G; Rossi G; Bugiani M; Bugiani O; Meloen R H; Collinge J; Tagliavini F; Ghetti B
An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathy.
The American journal of pathology 1998;152(6):1415-20.
1998: Spillantini M G; Bird T D; Ghetti B
Frontotemporal dementia and Parkinsonism linked to chromosome 17: a new group of tauopathies.
Brain pathology (Zurich, Switzerland) 1998;8(2):387-402.
1998: Salanova V; Markand O; Worth R; Smith R; Wellman H; Hutchins G; Park H; Ghetti B; Azzarelli B
FDG-PET and MRI in temporal lobe epilepsy: relationship to febrile seizures, hippocampal sclerosis and outcome.
Acta neurologica Scandinavica 1998;97(3):146-53.
1998: Brown P; Cervenáková L; McShane L; Goldfarb L G; Bishop K; Bastian F; Kirkpatrick J; Piccardo P; Ghetti B; Gajdusek D C
Creutzfeldt-Jakob disease in a husband and wife.
Neurology 1998;50(3):684-8.
1997: Migheli A; Piva R; Wei J; Attanasio A; Casolino S; Hodes M E; Dlouhy S R; Bayer S A; Ghetti B
Diverse cell death pathways result from a single missense mutation in weaver mouse.
The American journal of pathology 1997;151(6):1629-38.
1997: Bales K R; Verina T; Dodel R C; Du Y; Altstiel L; Bender M; Hyslop P; Johnstone E M; Little S P; Cummins D J; Piccardo P; Ghetti B; Paul S M
Lack of apolipoprotein E dramatically reduces amyloid beta-peptide deposition.
Nature genetics 1997;17(3):263-4.
1997: Murrell J R; Koller D; Foroud T; Goedert M; Spillantini M G; Edenberg H J; Farlow M R; Ghetti B
Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17.
American journal of human genetics 1997;61(5):1131-8.
1997: Wei J; Dlouhy S R; Bayer S; Piva R; Verina T; Wang Y; Feng Y; Dupree B; Hodes M E; Ghetti B
In situ hybridization analysis of Girk2 expression in the developing central nervous system in normal and weaver mice.
Journal of neuropathology and experimental neurology 1997;56(7):762-71.
1997: Won L; Ghetti B; Heller B; Heller A
In vitro evidence that the reduction in mesencephalic dopaminergic neurons in the weaver heterozygote is not due to a failure in target cell interaction.
Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale 1997;115(1):174-9.
1997: Park D W; Boldt H C; Massicotte S J; Akang E E; Roos K L; Bodnar A; Pless J; Ghetti B; Pascuzzi R M
Subacute sclerosing panencephalitis manifesting as viral retinitis: clinical and histopathologic findings.
American journal of ophthalmology 1997;123(4):533-42.
1997: Spillantini M G; Goedert M; Crowther R A; Murrell J R; Farlow M R; Ghetti B
Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(8):4113-8.
1997: Simon J R; Bare D J; Ghetti B; Richter J A
A possible role for tyrosine kinases in the regulation of the neuronal dopamine transporter in mouse striatum.
Neuroscience letters 1997;224(3):201-5.
1997: Unverzagt F W; Farlow M R; Norton J; Dlouhy S R; Young K; Ghetti B
Neuropsychological function in patients with Gerstmann-Sträussler-Scheinker disease from the Indiana kindred (F198S).
Journal of the International Neuropsychological Society : JINS 1997;3(2):169-78.
1997: Zhang W; Ghetti B; Lee W H
Decreased IGF-I gene expression during the apoptosis of Purkinje cells in pcd mice.
Brain research. Developmental brain research 1997;98(2):164-76.
1997: Young K; Clark H B; Piccardo P; Dlouhy S R; Ghetti B
Gerstmann-Sträussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129.
Brain research. Molecular brain research 1997;44(1):147-50.
1997: Verina T; Norton J A; Sorbel J J; Triarhou L C; Laferty D; Richter J A; Simon J R; Ghetti B
Atrophy and loss of dopaminergic mesencephalic neurons in heterozygous weaver mice.
Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale 1997;113(1):5-12.
1996: Piccardo P; Seiler C; Dlouhy S R; Young K; Farlow M R; Prelli F; Frangione B; Bugiani O; Tagliavini F; Ghetti B
Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred).
Journal of neuropathology and experimental neurology 1996;55(11):1157-63.
1996: Bayer S A; Wills K V; Wei J; Feng Y; Dlouhy S R; Hodes M E; Verina T; Ghetti B
Phenotypic effects of the weaver gene are evident in the embryonic cerebellum but not in the ventral midbrain.
Brain research. Developmental brain research 1996;96(1-2):130-7.
1996: Wei J; Hodes M E; Wang Y; Feng Y; Ghetti B; Dlouhy S R
Direct cDNA selection with DNA microdissected from mouse chromosome 16: isolation of novel clones and construction of a partial transcription map of the C3-C4 region.
Genome research 1996;6(8):678-87.
1996: Tong Y; Wei J; Zhang S; Strong J A; Dlouhy S R; Hodes M E; Ghetti B; Yu L
The weaver mutation changes the ion selectivity of the affected inwardly rectifying potassium channel GIRK2.
FEBS letters 1996;390(1):63-8.
1996: Perini F; Vidal R; Ghetti B; Tagliavini F; Frangione B; Prelli F
PrP27-30 is a normal soluble prion protein fragment released by human platelets.
Biochemical and biophysical research communications 1996;223(3):572-7.
1996: Parchi P; Castellani R; Capellari S; Ghetti B; Young K; Chen S G; Farlow M; Dickson D W; Sima A A; Trojanowski J Q; Petersen R B; Gambetti P
Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.
Annals of neurology 1996;39(6):767-78.
1996: Wei J; Dlouhy S R; Wang Y; Zhu J; Fitzpatrick L; Ghetti B; Hodes M E
Linkage mapping of microdissected clones from distal mouse chromosome 16.
Somatic cell and molecular genetics 1996;22(3):227-32.
1996: Wei J; Dlouhy S R; Hara A; Ghetti B; Hodes M E
Cloning a cDNA for carbonyl reductase (Cbr) from mouse cerebellum: murine genes that express cbr map to chromosomes 16 and 11.
Genomics 1996;34(1):147-8.
1996: Ghetti B; Piccardo P; Frangione B; Bugiani O; Giaccone G; Young K; Prelli F; Farlow M R; Dlouhy S R; Tagliavini F
Prion protein amyloidosis.
Brain pathology (Zurich, Switzerland) 1996;6(2):127-45.
1996: Lippa C F; Saunders A M; Smith T W; Swearer J M; Drachman D A; Ghetti B; Nee L; Pulaski-Salo D; Dickson D; Robitaille Y; Bergeron C; Crain B; Benson M D; Farlow M; Hyman B T; George-Hyslop S P; Roses A D; Pollen D A
Familial and sporadic Alzheimer's disease: neuropathology cannot exclude a final common pathway.
Neurology 1996;46(2):406-12.
1996: Ghetti B; Piccardo P; Spillantini M G; Ichimiya Y; Porro M; Perini F; Kitamoto T; Tateishi J; Seiler C; Frangione B; Bugiani O; Giaccone G; Prelli F; Goedert M; Dlouhy S R; Tagliavini F
Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.
Proceedings of the National Academy of Sciences of the United States of America 1996;93(2):744-8.
1995: Piccardo P; Ghetti B; Dickson D W; Vinters H V; Giaccone G; Bugiani O; Tagliavini F; Young K; Dlouhy S R; Seiler C
Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165.
Journal of neuropathology and experimental neurology 1995;54(6):790-801.
1995: Bare D J; Ghetti B; Richter J A
The tyrosine kinase inhibitor genistein increases endogenous dopamine release from normal and weaver mutant mouse striatal slices.
Journal of neurochemistry 1995;65(5):2096-104.
1995: Migheli A; Attanasio A; Lee W H; Bayer S A; Ghetti B
Detection of apoptosis in weaver cerebellum by electron microscopic in situ end-labeling of fragmented DNA.
Neuroscience letters 1995;199(1):53-6.
1995: Bayer S A; Wills K V; Triarhou L C; Verina T; Thomas J D; Ghetti B
Selective vulnerability of late-generated dopaminergic neurons of the substantia nigra in weaver mutant mice.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(20):9137-40.
1995: Stotz-Potter E H; Ghetti B; Simon J R
Endogenous serotonin release from the dopamine-deficient striatum of the weaver mutant mouse.
Neurochemical research 1995;20(7):821-6.
1995: Lee W H; Wang G M; Lo T; Triarhou L C; Ghetti B
Altered IGFBP5 gene expression in the cerebellar external germinal layer of weaver mutant mice.
Brain research. Molecular brain research 1995;30(2):259-68.
1995: Richter J A; Brenneman M G; Dlouhy S R; Ghetti B
Dopaminergic parameters in the striatum and substantia nigra of seven strains of mice: higher density in striatum of CAST compared to BALB mice.
Neurochemical research 1995;20(4):395-400.
1995: Verina T; Tang X; Fitzpatrick L; Norton J; Vogelweid C; Ghetti B
Degeneration of Sertoli and spermatogenic cells in homozygous and heterozygous weaver mice.
Journal of neurogenetics 1995;9(4):251-65.
1995: Richter J A; Bare D J; Yu H; Ghetti B; Simon J R
Dopamine transporter-dependent and -independent endogenous dopamine release from weaver mouse striatum in vitro.
Journal of neurochemistry 1995;64(1):191-8.
1995: Ghetti B; Dlouhy S R; Giaccone G; Bugiani O; Frangione B; Farlow M R; Tagliavini F
Gerstmann-Sträussler-Scheinker disease and the Indiana kindred.
Brain pathology (Zurich, Switzerland) 1995;5(1):61-75.
1995: Triarhou L C; Solà C; Mengod G; García-Ladona F J; Landwehrmeyer B; Ghetti B; Palacios J M
Ventral mesencephalic grafts in the neostriatum of the weaver mutant mouse: structural molecule and receptor studies.
Cell transplantation 1995;4(1):39-48.
1995: Suzuki K; Parker C C; Pentchev P G; Katz D; Ghetti B; D'Agostino A N; Carstea E D
Neurofibrillary tangles in Niemann-Pick disease type C.
Acta neuropathologica 1995;89(3):227-38.
1995: Bayer S A; Wills K V; Triarhou L C; Thomas J D; Ghetti B
Systematic differences in time of dopaminergic neuron origin between normal mice and homozygous weaver mutants.
Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale 1995;105(2):200-8.
1995: Bayer S A; Wills K V; Triarhou L C; Ghetti B
Time of neuron origin and gradients of neurogenesis in midbrain dopaminergic neurons in the mouse.
Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale 1995;105(2):191-9.
1994: Bayer S A; Triarhou L C; Thomas J D; Ghetti B
Correlated quantitative studies of the neostriatum, nucleus accumbens, substantia nigra, and ventral tegmental area in normal and weaver mutant mice.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1994;14(11 Pt 2):6901-10.
1994: Tagliavini F; Prelli F; Porro M; Rossi G; Giaccone G; Farlow M R; Dlouhy S R; Ghetti B; Bugiani O; Frangione B
Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele.
Cell 1994;79(4):695-703.
1994: Hodes M E; Dlouhy S R; Wei J J; Wang Y; Sangameswaran L; Lazar V; Triarhou L C; Ghetti B
cDNA approaches to isolation of the mouse mutant weaver gene.
Neurochemical research 1994;19(11):1359-62.
1994: Triarhou L C; Stotz E H; Low W C; Norton J; Ghetti B; Landwehrmeyer B; Palacios J M; Simon J R
Studies on the striatal dopamine uptake system of weaver mutant mice and effects of ventral mesencephalic grafts.
Neurochemical research 1994;19(11):1349-58.
1994: Wei J; Dlouhy S R; Zhu J; Ghetti B; Hodes M E
Analysis of region-specific library constructed by sequence-independent amplification of microdissected fragments surrounding weaver (wv) gene on mouse chromosome 16.
Somatic cell and molecular genetics 1994;20(5):401-8.
1994: Kambouris M; Sangameswaran L; Triarhou L C; Kozak C A; Dlouhy S R; Ghetti B; Hodes M E
Molecular characterization of a novel cDNA from murine cerebellum, developmental expression, and distribution in brain.
Brain research. Molecular brain research 1994;25(3-4):192-9.
1994: Kambouris M; Triarhou L C; Dlouhy S R; Sangameswaran L; Luo F; Ghetti B; Hodes M E
Novel cDNA clones obtained by antibody screening of a mouse cerebellar cDNA expression library.
Brain research. Molecular brain research 1994;25(3-4):183-91.
1994: Farlow M; Ghetti B; Dlouhy S; Giaccone G; Bugiani O; Tagliavini F; Wagner S
Cerebrospinal fluid levels of amyloid beta-protein precursor are low in Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
Neurology 1994;44(8):1508-10.
1994: Simon J R; Ghetti B
The weaver mutant mouse as a model of nigrostriatal dysfunction.
Molecular neurobiology 1994;9(1-3):183-9.
1994: Monari L; Chen S G; Brown P; Parchi P; Petersen R B; Mikol J; Gray F; Cortelli P; Montagna P; Ghetti B
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(7):2839-42.
1994: Ghetti B; Tagliavini F; Giaccone G; Bugiani O; Frangione B; Farlow M R; Dlouhy S R
Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.
Molecular neurobiology 1994;8(1):41-8.
1994: Simon J R; Richter J A; Ghetti B
Age-dependent alterations in dopamine content, tyrosine hydroxylase activity, and dopamine uptake in the striatum of the weaver mutant mouse.
Journal of neurochemistry 1994;62(2):543-8.
1994: Farlow M; Murrell J; Ghetti B; Unverzagt F; Zeldenrust S; Benson M
Clinical characteristics in a kindred with early-onset Alzheimer's disease and their linkage to a G-->T change at position 2149 of the amyloid precursor protein gene.
Neurology 1994;44(1):105-11.
1994: Stotz E H; Palacios J M; Landwehrmeyer B; Norton J; Ghetti B; Simon J R; Triarhou L C
Alterations in dopamine and serotonin uptake systems in the striatum of the weaver mutant mouse.
Journal of neural transmission. General section 1994;97(1):51-64.
1993: Liepnieks J J; Ghetti B; Farlow M; Roses A D; Benson M D
Characterization of amyloid fibril beta-peptide in familial Alzheimer's disease with APP717 mutations.
Biochemical and biophysical research communications 1993;197(2):386-92.
1993: Richter J A; Ghetti B; Simon J R
Dopamine-depleting effects of MPTP and reserpine in weaver mutant mice.
Molecular and chemical neuropathology / sponsored by the International Society for Neurochemistry and the World Federation of Neurology and research groups on neurochemistry and cerebrospinal fluid 1993;20(3):219-28.
1993: Vogelweid C M; Verina T; Norton J; Harruff R; Ghetti B
Hypospermatogenesis is the cause of infertility in the male weaver mutant mouse.
Journal of neurogenetics 1993;9(2):89-104.
1993: Solà C; Mengod G; Low W C; Norton J; Ghetti B; Palacios J M; Triarhou L C
Regional distribution of amyloid beta-protein precursor, growth-associated phosphoprotein-43 and microtubule-associated protein 2 messenger RNAs in the nigrostriatal system of normal and Weaver mutant mice and effects of ventral mesencephalic grafts.
The European journal of neuroscience 1993;5(11):1442-54.
1993: Tagliavini F; Prelli F; Verga L; Giaccone G; Sarma R; Gorevic P; Ghetti B; Passerini F; Ghibaudi E; Forloni G
Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro.
Proceedings of the National Academy of Sciences of the United States of America 1993;90(20):9678-82.
1993: Tagliavini F; Giaccone G; Prelli F; Verga L; Porro M; Trojanowski J Q; Farlow M R; Frangione B; Ghetti B; Bugiani O
A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
Brain research 1993;616(1-2):325-9.
1993: Kambouris M; Sangameswaran L; Dlouhy S R; Hodes M E; Ghetti B; Triarhou L C
Cellular distribution of the RNA transcripts of a newly discovered gene in the brain of normal, weaver, Purkinje cell degeneration and reeler mutant mice as evidenced by in situ hybridization histochemistry.
Brain research. Molecular brain research 1993;18(4):321-8.
1993: Zeldenrust S R; Murrell J; Farlow M; Ghetti B; Roses A D; Benson M D
RFLP analysis for APP 717 mutations associated with Alzheimer's disease.
Journal of medical genetics 1993;30(6):476-8.
1993: Simon J R; Ghetti B
Is there a significant somatodendritic uptake of dopamine in the substantia nigra? Evidence from the weaver mutant mouse.
Neurochemistry international 1993;22(5):471-7.
1993: Solà C; Mengod G; Ghetti B; Palacios J M; Triarhou L C
Regional distribution of the alternatively spliced isoforms of beta APP RNA transcript in the brain of normal, heterozygous and homozygous weaver mutant mice as revealed by in situ hybridization histochemistry.
Brain research. Molecular brain research 1993;17(3-4):340-6.
1993: Stotz E H; Triarhou L C; Ghetti B; Simon J R
Serotonin content is elevated in the dopamine deficient striatum of the weaver mutant mouse.
Brain research 1993;606(2):267-72.
1993: Bugiani O; Giaccone G; Verga L; Pollo B; Frangione B; Farlow M R; Tagliavini F; Ghetti B
Beta PP participates in PrP-amyloid plaques of Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
Journal of neuropathology and experimental neurology 1993;52(1):64-70.
1993: Chang A C; Ghetti B
Embryonic cerebellar graft development during acute phase of gliosis in the cerebellum of pcd mutant mice.
The Chinese journal of physiology 1993;36(3):141-9.
1992: Giaccone G; Verga L; Bugiani O; Frangione B; Serban D; Prusiner S B; Farlow M R; Ghetti B; Tagliavini F
Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(19):9349-53.
1992: Farlow M; Ghetti B; Benson M D; Farrow J S; van Nostrand W E; Wagner S L
Low cerebrospinal-fluid concentrations of soluble amyloid beta-protein precursor in hereditary Alzheimer's disease.
Lancet 1992;340(8817):453-4.
1992: Triarhou L C; Low W C; Ghetti B
Serotonin fiber innervation of cerebellar cell suspensions intraparenchymally grafted to the cerebellum of pcd mutant mice.
Neurochemical research 1992;17(5):475-82.
1992: Simon J R; Ghetti B
Topographic distribution of dopamine uptake, choline uptake, choline acetyltransferase, and GABA uptake in the striata of weaver mutant mice.
Neurochemical research 1992;17(5):431-6.
1992: Richter J A; Stotz E H; Ghetti B; Simon J R
Comparison of alterations in tyrosine hydroxylase, dopamine levels, and dopamine uptake in the striatum of the weaver mutant mouse.
Neurochemical research 1992;17(5):437-41.
1992: Hsiao K; Dlouhy S R; Farlow M R; Cass C; Da Costa M; Conneally P M; Hodes M E; Ghetti B; Prusiner S B
Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.
Nature genetics 1992;1(1):68-71.
1992: Dlouhy S R; Hsiao K; Farlow M R; Foroud T; Conneally P M; Johnson P; Prusiner S B; Hodes M E; Ghetti B
Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene.
Nature genetics 1992;1(1):64-7.
1992: Ghetti B; Triarhou L C
Degeneration of mesencephalic dopamine neurons in weaver mutant mice.
Neurochemistry international 1992;20 Suppl():305S-307S.
1992: Yee R D; Farlow M R; Suzuki D A; Betelak K F; Ghetti B
Abnormal eye movements in Gerstmann-Sträussler-Scheinker disease.
Archives of ophthalmology 1992;110(1):68-74.
1992: Ghetti B; Murrell J; Benson M D; Farlow M R
Spectrum of amyloid beta-protein immunoreactivity in hereditary Alzheimer disease with a guanine to thymine missense change at position 1924 of the APP gene.
Brain research 1992;571(1):133-9.
1992: Triarhou L C; Low W C; Ghetti B
Intraparenchymal grafting of cerebellar cell suspensions to the deep cerebellar nuclei of pcd mutant mice, with particular emphasis on re-establishment of a Purkinje cell cortico-nuclear projection.
Anatomy and embryology 1992;185(5):409-20.
1991: Simon J R; Yu H; Richter J A; Vasko M R; Ghetti B
In vitro release of endogenous dopamine from the striatum of the weaver mutant mouse.
Journal of neurochemistry 1991;57(5):1478-82.
1991: Triarhou L C; Ghetti B
Serotonin-immunoreactivity in the cerebellum of two neurological mutant mice and the corresponding wild-type genetic stocks.
Journal of chemical neuroanatomy 1991;4(6):421-8.
1991: Murrell J; Farlow M; Ghetti B; Benson M D
A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease.
Science (New York, N.Y.) 1991;254(5028):97-9.
1991: Bugiani O; Constantinidis J; Ghetti B; Bouras C; Tagliavini F
Asymmetrical cerebral atrophy in Alzheimer's disease.
Clinical neuropathology 1991;10(2):55-60.
1991: Tagliavini F; Prelli F; Ghiso J; Bugiani O; Serban D; Prusiner S B; Farlow M R; Ghetti B; Frangione B
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.
The EMBO journal 1991;10(3):513-9.
1991: Ghetti B; Triarhou L C; Alyea C J; Dlouhy S R; Karn R C
Unique cerebellar phenotype combining granule and Purkinje cell loss: morphological evidence for weaver* pcd double mutant mice.
Journal of neurocytology 1991;20(1):27-38.
1991: Triarhou L C; Ghetti B
Stabilisation of neurone number in the inferior olivary complex of aged 'Purkinje cell degeneration' mutant mice.
Acta neuropathologica 1991;81(6):597-602.
1990: Giaccone G; Tagliavini F; Verga L; Frangione B; Farlow M R; Bugiani O; Ghetti B
Neurofibrillary tangles of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease share antigenic determinants with those of Alzheimer disease.
Brain research 1990;530(2):325-9.
1990: Bugiani O; Giaccone G; Verga L; Pollo B; Ghetti B; Frangione B; Tagliavini F
Alzheimer patients and Down patients: abnormal presynaptic terminals are related to cerebral preamyloid deposits.
Neuroscience letters 1990;119(1):56-9.
1990: Ghetti B; Triarhou L C; Alyea C J; Low W C; Chang A C
Timing of neuronal replacement in cerebellar degenerative ataxia of Purkinje cell type.
Progress in brain research 1990;82():197-202.
1990: Triarhou L C; Low W C; Ghetti B
Dopamine neurone grafting to the weaver mouse neostriatum.
Progress in brain research 1990;82():187-95.
1990: Kaseda Y; Ghetti B; Low W C; Norton J; Brittain H; Triarhou L C; Richter J A; Simon J R
Age-related changes in striatal dopamine D2 receptor binding in weaver mice and effects of ventral mesencephalic grafts.
Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale 1990;83(1):1-8.
1990: Triarhou L C; Brundin P; Doucet G; Norton J; Björklund A; Ghetti B
Intrastriatal implants of mesencephalic cell suspensions in weaver mutant mice: ultrastructural relationships of dopaminergic dendrites and axons issued from the graft.
Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale 1990;79(1):3-17.
1989: Farlow M R; Yee R D; Dlouhy S R; Conneally P M; Azzarelli B; Ghetti B
Gerstmann-Sträussler-Scheinker disease. I. Extending the clinical spectrum.
Neurology 1989;39(11):1446-52.
1989: Triarhou L C; Ghetti B
The dendritic dopamine projection of the substantia nigra: phenotypic denominator of weaver gene action in hetero- and homozygosity.
Brain research 1989;501(2):373-81.
1989: Ghetti B; Tagliavini F; Masters C L; Beyreuther K; Giaccone G; Verga L; Farlow M R; Conneally P M; Dlouhy S R; Azzarelli B
Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family.
Neurology 1989;39(11):1453-61.
1989: Bugiani O; Giaccone G; Frangione B; Ghetti B; Tagliavini F
Alzheimer patients: preamyloid deposits are more widely distributed than senile plaques throughout the central nervous system.
Neuroscience letters 1989;103(3):263-8.
1989: Chang A C; Triarhou L C; Alyea C J; Low W C; Ghetti B
Developmental expression of polypeptide PEP-19 in cerebellar cell suspensions transplanted into the cerebellum of pcd mutant mice.
Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale 1989;76(3):639-45.
1989: Doucet G; Brundin P; Seth S; Murata Y; Strecker R E; Triarhou L C; Ghetti B; Björklund A
Degeneration and graft-induced restoration of dopamine innervation in the weaver mouse neostriatum: a quantitative radioautographic study of [3H]dopamine uptake.
Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale 1989;77(3):552-68.
1988: Triarhou L C; Low W C; Ghetti B
Layer-specific innervation of the dopamine-deficient frontal cortex in weaver mutant mice by grafted mesencephalic dopaminergic neurones.
Cell and tissue research 1988;254(1):11-5.
1988: Mendelsohn L G; Smith M C; Lucaites V L; Kerchner G A; Ghetti B
Autoradiographic localization of insulin-like growth factor II receptors in cerebellar cortex of weaver and Purkinje cell degeneration mutant mice.
Brain research 1988;458(2):361-6.
1988: Ghetti B; Perry K W; Fuller R W
Serotonin concentration and turnover in cerebellum and other brain regions of pcd mutant mice.
Brain research 1988;458(2):367-71.
1988: Triarhou L C; Low W C; Norton J; Ghetti B
Reinstatement of synaptic connectivity in the striatum of weaver mutant mice following transplantation of ventral mesencephalic anlagen.
Journal of neurocytology 1988;17(2):233-43.
1988: Triarhou L C; Norton J; Ghetti B
Synaptic connectivity of tyrosine hydroxylase immunoreactive nerve terminals in the striatum of normal, heterozygous and homozygous weaver mutant mice.
Journal of neurocytology 1988;17(2):221-32.
1988: McBride W J; Ghetti B
Changes in the content of glutamate and GABA in the cerebellar vermis and hemispheres of the Purkinje cell degeneration (pcd) mutant.
Neurochemical research 1988;13(2):121-5.
1988: Triarhou L C; Norton J; Ghetti B
Mesencephalic dopamine cell deficit involves areas A8, A9 and A10 in weaver mutant mice.
Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale 1988;70(2):256-65.
1988: Giaccone G; Tagliavini F; Street J S; Ghetti B; Bugiani O
Progressive supranuclear palsy with hypertrophy of the olives. An immunocytochemical study of the cytoskeleton of argyrophilic neurons.
Acta neuropathologica 1988;77(1):14-20.
1987: Triarhou L C; Low W C; Ghetti B
Synaptic investment of striatal cellular domains by grafted dopamine neurons in weaver mutant mice.
Die Naturwissenschaften 1987;74(12):591-3.
1987: Low W C; Triarhou L C; Kaseda Y; Norton J; Ghetti B
Functional innervation of the striatum by ventral mesencephalic grafts in mice with inherited nigrostriatal dopamine deficiency.
Brain research 1987;435(1-2):315-21.
1987: Kaseda Y; Ghetti B; Low W C; Richter J A; Simon J R
Dopamine D2 receptors increase in the dorsolateral striatum of weaver mutant mice.
Brain research 1987;422(1):178-81.
1987: Ghetti B; Norton J; Triarhou L C
Nerve cell atrophy and loss in the inferior olivary complex of "Purkinje cell degeneration" mutant mice.
The Journal of comparative neurology 1987;260(3):409-22.
1987: Hofstetter J R; Vincent I; Bugiani O; Ghetti B; Richter J A
Aluminum-induced decreases in choline acetyltransferase, tyrosine hydroxylase, and glutamate decarboxylase in selected regions of rabbit brain.
Neurochemical pathology 1987;6(3):177-93.
1987: Gupta M; Felten D L; Ghetti B
Selective loss of monoaminergic neurons in weaver mutant mice--an immunocytochemical study.
Brain research 1987;402(2):379-82.
1987: Triarhou L C; Ghetti B
Neuroanatomical substrate of behavioural impairment in weaver mutant mice.
Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale 1987;68(2):434-6.
1987: Triarhou L C; Low W C; Ghetti B
Transplantation of cerebellar anlagen to hosts with genetic cerebellocortical atrophy.
Anatomy and embryology 1987;176(2):145-54.
1987: Triarhou L C; Norton J; Ghetti B
Anterograde transsynaptic degeneration in the deep cerebellar nuclei of Purkinje cell degeneration (pcd) mutant mice.
Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale 1987;66(3):577-88.
1986: Triarhou L C; Low W C; Ghetti B
Transplantation of ventral mesencephalic anlagen to hosts with genetic nigrostriatal dopamine deficiency.
Proceedings of the National Academy of Sciences of the United States of America 1986;83(22):8789-93.
1986: Triarhou L C; Ghetti B
Monoaminergic nerve terminals in the cerebellar cortex of Purkinje cell degeneration mutant mice: fine structural integrity and modification of cellular environs following loss of Purkinje and granule cells.
Neuroscience 1986;18(4):795-807.
1986: Felten D L; Felten S Y; Perry K W; Fuller R W; Nurnberger J I; Ghetti B
Noradrenergic innervation of the cerebellar cortex in normal and in Purkinje cell degeneration mutant mice: evidence for long term survival following loss of the two major cerebellar cortical neuronal populations.
Neuroscience 1986;18(4):783-93.
1985: Triarhou L C; Norton J; Bugiani O; Ghetti B
Ventral root axonopathy and its relation to the neurofibrillary degeneration of lower motor neurons in aluminum-induced encephalomyelopathy.
Neuropathology and applied neurobiology 1985;11(6):407-30.
1985: Vaccarino F M; Ghetti B; Nurnberger J I
Residual benzodiazepine (BZ) binding in the cortex of pcd mutant cerebella and qualitative BZ binding in the deep cerebellar nuclei of control and mutant mice: an autoradiographic study.
Brain research 1985;343(1):70-8.
1985: Sato Y; Kim S U; Ghetti B
Induction of neurofibrillary tangles in cultured mouse neurons by maytanprine.
Journal of the neurological sciences 1985;68(2-3):191-203.
1985: Ghetti B; Musicco M; Norton J; Bugiani O
Nerve cell loss in the progressive encephalopathy induced by aluminum powder. A morphologic and semiquantitative study of the Purkinje cells.
Neuropathology and applied neurobiology 1985;11(1):31-53.
1985: Bugiani O; Brancaccio D; Ghetti B
Progressive dialytic encephalopathy and the problem of aluminum neurotoxicity.
Clinical nephrology 1985;24 Suppl 1():S20-5.
1985: Azzarelli B; Muller J; Ghetti B; Dyken M; Conneally P M
Cerebellar plaques in familial Alzheimer's disease (Gerstmann-Sträussler-Scheinker variant?).
Acta neuropathologica 1985;65(3-4):235-46.
1983: Ghetti B; Gambetti P
Comparative immunocytochemical characterization of neurofibrillary tangles in experimental maytansine and aluminum encephalopathies.
Brain research 1983;276(2):388-93.
1983: Gambetti P; Shecket G; Ghetti B; Hirano A; Dahl D
Neurofibrillary changes in human brain. An immunocytochemical study with a neurofilament antiserum.
Journal of neuropathology and experimental neurology 1983;42(1):69-79.
1983: Vaccarino F M; Ghetti B; Wade S E; Rea M A; Aprison M H
Loss of Purkinje cell-associated benzodiazepine receptors spares a high affinity subpopulation: a study with pcd mutant mice.
Journal of neuroscience research 1983;9(3):311-23.
1982: Schmidt M J; Sawyer B D; Perry K W; Fuller R W; Foreman M M; Ghetti B
Dopamine deficiency in the weaver mutant mouse.
The Journal of neuroscience : the official journal of the Society for Neuroscience 1982;2(3):376-80.
1982: Bugiani O; Ghetti B
Progressing encephalomyelopathy with muscular atrophy, induced by aluminum powder.
Neurobiology of aging 1982;3(3):209-22.
1982: Schwartz J P; Ghetti B; Truex L; Schmidt M J
Increase of a nerve growth factor-like protein in the cerebellum of PCD mutant mice.
Journal of neuroscience research 1982;8(2-3):205-11.
1981: Ghetti B; Fuller R W; Sawyer B D; Hemrick-Luecke S K; Schmidt M J
Purkinje cell loss and the noradrenergic system in the cerebellum of pcd mutant mice.
Brain research bulletin 1981;7(6):711-4.
1981: Routtenberg A; Morgan D G; Conway R G; Schmidt M J; Ghetti B
Human brain protein phosphorylation in vitro: cyclic AMP stimulation of electrophoretically-separated substrates.
Brain research 1981;222(2):323-33.
1981: Ghetti B; Truex L; Sawyer B; Strada S; Schmidt M
Exaggerated cyclic AMP accumulation and glial cell reaction in the cerebellum during Purkinje cell degeneration in pcd mutant mice.
Journal of neuroscience research 1981;6(6):789-901.
1980: Schmidt M J; Truex L L; Ghetti B; Routtenberg A
Cyclic AMP-dependent protein kinase activity in human brain across age.
Journal of neurochemistry 1980;35(1):261-5.
1980: Kim S U; Tomonaga M; Ghetti B
Neurofibrillary degeneration in cultured adult mouse neurons induced by maytansine.
Acta neuropathologica 1980;52(2):161-4.
1980: Schmidt M J; Ghetti B
Exaggerated norepinephrine-stimulated accumulation of cyclic AMP in vitro in cerebellar slices from pcd mutant mice following Purkinje cell loss.
Journal of neural transmission 1980;48(1):49-56.
1979: Ghetti B
Induction of neurofibrillary degeneration following treatment with maytansine in vivo.
Brain research 1979;163(1):9-19.
1979: Maggi A; Schmidt M J; Ghetti B; Enna S J
Effect of aging on neurotransmitter receptor binding in rat and human brain.
Life sciences 1979;24(4):367-73.
1975: Ghetti B; Horoupian D S; Wisniewski H M
Acute and long-term transneuronal response of dendrites of lateral geniculate neurons following transection of the primary visual afferent pathway.
Advances in neurology 1975;12():401-24.
1974: Korthals J K; Wisniewski H M; Ghetti B; Cook R D
The fate of the axon and its terminal in the Pacinian corpuscle following sciatic nerve section.
Journal of neurocytology 1974;3(3):385-403.
1974: Cook R D; Ghetti B; Wisniewski H M
The pattern of Wallerian degeneration in the optic nerve of newborn kittens: an ultrastructural study.
Brain research 1974;75(2):261-75.
1974: Kristensson K; Ghetti B; Wisniewski H M
Study on the propagation of Herpes simplex virus (type 2) into the brain after intraocular injection.
Brain research 1974;69(2):189-201.
1973: Wisniewski H M; Ghetti B; Terry R D
Neuritic (senile) plaques and filamentous changes in aged rhesus monkeys.
Journal of neuropathology and experimental neurology 1973;32(4):566-84.
1973: Guazzi G C; Ghetti B; Barbieri F; Cecio A
Mycolonus epilepsy with cherry-red spot in adult: a peculiar form of mucopolysaccharidosis. (A clinical genetic, chemical and ultrastructural study).
Acta neurologica 1973;28(5):542-9.
1973: Horoupian D S; Ghetti B; Wisniewski H M
Retrograde transneuronal degeneration of optic fibers and their terminals in lateral geniculate nucleus of rhesus monkey.
Brain research 1973;49(2):257-75.
1972: Wisniewski H M; Ghetti B; Horoupian D S
The fate of synaptic membranes of degenerating optic nerve terminals, and their role in the mechanism of trans-synaptic changes.
Journal of neurocytology 1972;1(3):297-310.
1972: Ghetti B; Horoupian D S; Wisniewski H M
Transsynaptic response of the lateral geniculate nucleus and the pattern of degeneration of the nerve terminals in the rhesus monkey after eye enucleation.
Brain research 1972;45(1):31-48.
1972: Ghetti B; Wisniewski H M
On degeneration of terminals in the cat striate cortex.
Brain research 1972;44(2):630-5.
1971: Raine C S; Ghetti B; Shelanski M L
On the association between microtubules and mitochondria within axons.
Brain research 1971;34(2):389-93.
1971: Bravaccio F; Del Vecchio M; Paolozzi C; Ghetti B; Tripaldelli B; Amati A; Guazzi G C
[Late cerebellar atrophy with osteo-tendinous areflexia and progressive ophthalmoplegia with dominant autosomal heredity. Long-term study in 6 generations of one family]
Acta neurologica 1971;26(3):361-74.
1971: Del Vecchio M; Cerillo A; Ghetti B; Amati A; Signorelli C; Cedrola G; Guazzi G C
[Genetic study of 2 families (23 subjects) with von Recklinghausen's disease with dominant autosomal heredity]
Acta neurologica 1971;26(3):319-60.
1971: Ghetti B; Amati A; Turra M V; Pacini A; Del Vecchio M; Guazzi G C
Werdnig-Hoffmann-Wohlfart-Kugelberg-Welander disease. Nosological unity and clinical variability in intrafamilial cases.
Acta geneticae medicae et gemellologiae 1971;20(1):43-58.
1970: Guazzi G C; Ventruto V; Del Vecchio M; Fazzi G R; Ghetti B; Salvati G; Vertucci P; Bianchi A
[Genetic and immunologic study of 2 families affected by ataxia-telangiectastia of Mme Louis-Bar]
Acta neurologica 1970;25(5):551-77.
1970: Cecio A; Ghetti B; De Masi R V; Guazzi G C
[Ultrastructure of hepatic biopsy in a 29-year-old patient with epilepsy-myoclonus with cherry red spots in the fundus oculi]
Bollettino della Società italiana di biologia sperimentale 1970;46(9):457-9.
1970: Ghetti B; Cecio A; De Masi R V; Guazzi G C
[Histological and histochemical study of hepatic biopsy in a 29-year-old patient with epilepsy-myoclonus with cherry red spots in the fundus oculi]
Bollettino della Società italiana di biologia sperimentale 1970;46(9):455-7.
1970: Guazzi G C; Ghetti B; Del Vecchio M; Striano S
[Genetic study of a family with juvenile myoclonus-epilepsy with cherry red spots in the fundus oculi]
Bollettino della Società italiana di biologia sperimentale 1970;46(9):452-5.
1970: Fiore C; Ghetti B; Bertolino A; Fazzi R; Guazzi G C
[Louis-Bar ataxia telangiectasia: study of the first Italian case]
Rassegna internazionale di clinica e terapia 1970;50(10):599-601.
1970: Ghetti B; Guazzi G C; De Masi R V; Cecio A
[Juvenile myoclonic epilepsy with cherry-red spot in the fundus oculi. II. Histological and ultrastructural study of the hepatic biopsy]
Acta neurologica 1970;25(2):252-60.
1969: Bertolino A; Fiore C; Morcaldi L; Pinto L; Ghetti B; Guazzi G C
[Congenital generalized erythematous telangiectasis of Bloom associated with osteo-tendineous areflexia and oligophrenia: the 1st case in Italy]
Rassegna internazionale di clinica e terapia 1969;49(21):1331-47.
1969: Cassano G B; Viola P L; Ghetti B; Amaducci L
The distribution of inhaled mercury(Hg203) vapors in the brain of rats and mice.
Journal of neuropathology and experimental neurology 1969;28(2):308-20.
1967: Cassano G B; Ghetti B; Gliozzi E; Hansson E
Autoradiographic distribution study of "short acting" and "long acting" barbiturates: 35S-thiopentone and 14C-phenobarbitone.
British journal of anaesthesia 1967;39(1):11-20.
1967: Cassano G B; Placidi G F; Ghetti B
[Comparative study of the fetal distribution of some psychotropic and hypnotic drugs]
Rivista di neurobiologia : organo ufficiale della Società dei neurologi, neuroradiologi e neurochirurghi ospedalieri 1967;13(1):105-14.

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