Bernardino Ghetti

School of Medicine, Pathology & Laboratory Medicine

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Bernardino Ghetti

• School of Medicine
  School of Medicine
  
  Pathology & Laboratory Medicine
  
  

  Current Appointments:

  Professor of Pathology & Laboratory Medicine

  
  
  

This is a list of publications by this researcher, listed chronologically starting with the most recent first. New publications appear in this list weekly. The source of publications and 'cited by' data for this application is Scopus.

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• 1.

  2013

  S. Spina; A.D. Van Laar; J.R. Murrell; R.L. Hamilton; J.K. Kofler; F. Epperson; M.R. Farlow; O.L. Lopez; J. Quinlan; S.T. Dekosky; et al.

  Phenotypic variability in three families with valosin-containing protein mutation

  European Journal of Neurology. 2013;20(2):251-258.
  1

• 2.

  2013

  Alejandra del Carmen Alonso; Ezzat ElAkkad; ChengXin Gong; Fei Liu; Toshihisa Tanaka; Takashi Kudo; Yositaka Tatebayashi; JinJing Pei; JiangZhi Wang; Sabiha Khatoon; et al.

  Erratum to: Inge Grundke-Iqbal, Ph.D. (1937-2012): the Discoverer of the Abnormal Hyperphosphorylation of Tau in Alzheimer's Disease

  Journal of Molecular Neuroscience. 2013:1-2.
  0

• 3.

  2013

  Maria Luisa Moro; Giorgio Giaccone; Raffaella Lombardi; Antonio Indaco; Andrea Uggetti; Michela Morbin; Stefania Saccucci; Giuseppe Di Fede; Marcella Catania; Dominic M. Walsh; et al.

  Erratum to: APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38

  Acta Neuropathologica. 2013:1.
  0

• 4.

  2013

  Holly J. Garringer; Jill Murrell; Neeraja Sammeta; Anita Gnezda; Bernardino Ghetti; Ruben Vidal

  Increased Tau Phosphorylation and Tau Truncation, and Decreased Synaptophysin Levels in Mutant BRI₂/Tau Transgenic Mice

  PLoS ONE. 2013;8(2).
  0

• 5.

  2012

  Martin Jeffrey; Gillian McGovern; Emily V. Chambers; Declan King; Lorenzo González; Jean C. Manson; Bernardino Ghetti; Pedro Piccardo; Rona M. Barron

  Mechanism of PrP-amyloid formation in mice without transmissible spongiform encephalopathy

  Brain Pathology. 2012;22(1):58-66.
  3

• 6.

  2012

  Rosa Rademakers; Matt Baker; Alexandra M. Nicholson; Nicola J. Rutherford; Nicole Finch; Alexandra Soto-Ortolaza; Jennifer Lash; Christian Wider; Aleksandra Wojtas; Mariely Dejesus-Hernandez; et al.

  Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

  Nature Genetics. 2012;44(2):200-205.
  22

• 7.

  2012

  Salvatore Monaco; Michele Fiorini; Alessia Farinazzo; Sergio Ferrari; Matteo Gelati; Pedro Piccardo; Gianluigi Zanusso; Bernardino Ghetti

  Allelic origin of protease-sensitive and protease-resistant prion protein isoforms in gerstmann-sträussler-scheinker disease with the p102l mutation

  PLoS ONE. 2012;7(2).
  0

• 8.

  2012

  Raffaele Ferrari; Kin Mok; Jorge H. Moreno; Stephanie Cosentino; Jill Goldman; Pietro Pietrini; Richard Mayeux; Michael C. Tierney; Dimitrios Kapogiannis; Gregory A. Jicha; et al.

  Screening for C9ORF72 repeat expansion in FTLD

  Neurobiology of Aging. 2012;33(8):e1-e11.
  3

• 9.

  2012

  Ruben Vidal; Neeraja Sammeta; Holly J. Garringer; Kumar Sambamurti; Leticia Miravalle; Bruce T. Lamb; Bernardino Ghetti

  The Psen1-L166P-knock-in mutation leads to amyloid deposition in human wild-type amyloid precursor protein YAC transgenic mice

  FASEB Journal. 2012;26(7):2899-2910.
  2

• 10.

  2012

  Giovanni Coppola; Subashchandrabose Chinnathambi; Jason JiYong Lee; Beth A. Dombroski; Matt C. Baker; Alexandra I. Soto-ortolaza; Suzee E. Lee; Eric Klein; Alden Y. Huang; Renee Sears; et al.

  Evidence for a role of the rare p.A152T variant in mapt in increasing the risk for FTD-spectrum and Alzheimer's diseases

  Human Molecular Genetics. 2012;21(15):3500-3512.
  3

• 11.

  2012

  Randall J. Bateman; Chengjie Xiong; Tammie L. S. Benzinger; Anne M. Fagan; Alison Goate; Nick C. Fox; Daniel S. Marcus; Nigel J. Cairns; Xianyun Xie; Tyler M. Blazey; et al.

  Clinical and biomarker changes in dominantly inherited Alzheimer's disease

  New England Journal of Medicine. 2012;367(9):795-804.
  53

• 12.

  2012

  Christina Sundal; Jay A. Van Gerpen; Alexandra M. Nicholson; Christian Wider; Elizabeth A. Shuster; Jan Aasly; Salvatore Spina; Bernardino Ghetti; Sigrun Roeber; James Garbern; et al.

  MRI characteristics and scoring in HDLS due to CSF1R gene mutations

  Neurology. 2012;79(6):566-574.
  1

• 13.

  2012

  Rubén Vidal; Bernardino Ghetti

  Generation of a novel murine model of Aβ deposition based on the expression of human wild-type amyloid precursor protein gene

  Prion. 2012;6(4):346-349.
  0

• 14.

  2012

  Maria Luisa Moro; Giorgio Giaccone; Raffaella Lombardi; Antonio Indaco; Andrea Uggetti; Michela Morbin; Stefania Saccucci; Giuseppe Di Fede; Marcella Catania; Dominic M. Walsh; et al.

  APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38

  Acta Neuropathologica. 2012:1-13.
  0

• 15.

  2012

  David C. Whitcomb; Jessica LaRusch; Alyssa M. Krasinskas; Lambertus Klei; Jill P. Smith; Randall E. Brand; John P. Neoptolemos; Markus M. Lerch; Matt Tector; Bimaljit S. Sandhu; et al.

  Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis

  Nature Genetics. 2012;44(12):1349-1354.
  0

• 16.

  2011

  Ellen M. Wijsman; Nathan D. Pankratz; Yoonha Choi; Joseph H. Rothstein; Kelley M. Faber; Rong Cheng; Joseph H. Lee; Thomas D. Bird; David A. Bennett; Ramon Diaz-Arrastia; et al.

  Genome-wide association of familial late-onset alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE

  PLoS Genetics. 2011;7(2).
  26

• 17.

  2011

  Alice S. Chen-Plotkin; Maria Martinez-Lage; Patrick M. A. Sleiman; William Hu; Robert Greene; Elisabeth McCarty Wood; Shaoxu Bing; Murray Grossman; Gerard D. Schellenberg; Kimmo J. Hatanpaa; et al.

  Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration

  Archives of Neurology. 2011;68(4):488-497.
  16

• 18.

  2011

  Suman Jayadev; David Nochlin; Parvoneh Poorkaj; Ellen J. Steinbart; James A. Mastrianni; Thomas J. Montine; Bernardino Ghetti; Gerard D. Schellenberg; Thomas D. Bird; James B. Leverenz

  Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype

  Annals of Neurology. 2011;69(4):712-720.
  8

• 19.

  2011

  Adam C. Naj; Gyungah Jun; Gary W. Beecham; Li-San Wang; Badri Narayan Vardarajan; Jacqueline Buros; Paul J. Gallins; Joseph D. Buxbaum; Gail P. Jarvik; Paul K. Crane; et al.

  Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

  Nature Genetics. 2011;43(5):436-443.
  189

• 20.

  2011

  Arianna Bellucci; Orso Bugiani; Bernardino Ghetti; Maria Grazia Spillantini

  Presence of reactive microglia and neuroinflammatory mediators in a case of frontotemporal dementia with P301S mutation

  Neurodegenerative Diseases. 2011;8(4):221-229.
  2

• 21.

  2011

  Günter U. Höglinger; Nadine M. Melhem; Dennis W. Dickson; Patrick M. A. Sleiman; Li-San Wang; Lambertus Klei; Rosa Rademakers; Rohan De Silva; Irene Litvan; David E. Riley; et al.

  Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

  Nature Genetics. 2011;43(7):699-705.
  41

• 22.

  2011

  Alberto J. Espay; Salvatore Spina; David J. Houghton; Jill R. Murrell; Gabrielle M. De Courten-Myers; Bernardino Ghetti; Irene Litvan

  Rapidly progressive atypical parkinsonism associated with frontotemporal lobar degeneration and motor neuron disease

  Journal of Neurology, Neurosurgery and Psychiatry. 2011;82(7):751-753.
  0

• 23.

  2011

  Matthew C. Hagen; Jill R. Murrell; Marie-Bernadette Delisle; Eva Andermann; Frederick Andermann; Marie Christine Guiot; Bernardino Ghetti

  Encephalopathy with neuroserpin inclusion bodies presenting as progressive myoclonus epilepsy and associated with a novel mutation in the Proteinase Inhibitor 12 gene

  Brain Pathology. 2011;21(5):575-582.
  3

• 24.

  2011

  Ruben Vidal; Bernardino Ghetti

  Characterization of amyloid deposits in neurodegenerative diseases

  Methods in Molecular Biology. 2011;793:241-258.
  1

• 25.

  2011

  Bernardino Ghetti

  Introduction: From the desk of the guest editor

  Journal of Molecular Neuroscience. 2011;45(3):321-322.
  0

• 26.

  2010

  S. Albrecht; N. Bogdanovic; B. Ghetti; B. Winblad; A. Leblanc

  Erratum: Caspase-6 activation in familial alzheimer disease brains carrying amyloid precursor protein or pesenilin I or presenilin II mutations (Journal of Neuropathology and Experimental Neurology (2009) 68 (1282-1293)

  Journal of Neuropathology and Experimental Neurology. 2010;69(1):110.
  0

• 27.

  2010

  Chiara Cupidi; Raffaella Capobianco; Donato Goffredo; Gabriella Marcon; Bernardino Ghetti; Orso Bugiani; Fabrizio Tagliavini; Giorgio Giaccone

  Neocortical variation of Aβ load in fully expressed, pure Alzheimer's disease

  Journal of Alzheimer's Disease. 2010;19(1):57-68.
  4

• 28.

  2010

  Vladimir Kepe; Bernardino Ghetti; Martin R. Farlow; Mara Bresjanac; Karen Miller; Sung-Cheng Huang; Koon-Pong Wong; Jill R. Murrell; Pedro Piccardo; Francine Epperson; et al.

  PET of brain prion protein amyloid in Gerstmann-Sträussler-Scheinker disease

  Brain Pathology. 2010;20(2):419-430.
  14

• 29.

  2010

  Vivianna M. Van Deerlin; Patrick M. A. Sleiman; Maria Martinez-Lage; Alice Chen-Plotkin; Li-San Wang; Neill R. Graff-Radford; Dennis W. Dickson; Rosa Rademakers; Bradley F. Boeve; Murray Grossman; et al.

  Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

  Nature Genetics. 2010;42(3):234-239.
  88

• 30.

  2010

  Ian R. A. MacKenzie; Manuela Neumann; Eileen H. Bigio; Nigel J. Cairns; Irina Alafuzoff; Jillian Kril; Gabor G. Kovacs; Bernardino Ghetti; Glenda Halliday; Ida E. Holm; et al.

  Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: An update

  Acta Neuropathologica. 2010;119(1):1-4.
  199

• 31.

  2010

  Holly J. Garringer; Jill Murrell; Luciano D'Adamio; Bernardino Ghetti; Ruben Vidal

  Modeling familial British and Danish dementia

  Brain Structure and Function. 2010;214(2-3):235-244.
  7

• 32.

  2010

  Pablo Garcia-Reitböck; Oleg Anichtchik; Arianna Bellucci; Mariangela Iovino; Chiara Ballini; Elena Fineberg; Bernardino Ghetti; Laura Della Corte; Pierfranco Spano; George K. Tofaris; et al.

  SNARE protein redistribution and synaptic failure in a transgenic mouse model of Parkinson's disease

  Brain. 2010;133(7):2032-2044.
  38

• 33.

  2010

  Piero Parchi; Maura Cescatti; Silvio Notari; Walter J. Schulz-Schaeffer; Sabina Capellari; Armin Giese; Wen-Quan Zou; Hans Kretzschmar; Bernardino Ghetti; Paul Brown

  Agent strain variation in human prion disease: Insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease

  Brain. 2010;133(10):3030-3042.
  15

• 34.

  2010

  Ana G. Barbeito; Thierry Levade; Marie B. Delisle; Bernardino Ghetti; Ruben Vidal

  Abnormal iron metabolism in fibroblasts from a patient with the neurodegenerative disease hereditary ferritinopathy

  Molecular Neurodegeneration. 2010;5(1).
  2

• 35.

  2009

  Ian R.A. Mackenzie; Manuela Neumann; Eileen H. Bigio; Nigel J. Cairns; Irina Alafuzoff; Jillian Kril; Gabor G. Kovacs; Bernardino Ghetti; Glenda Halliday; Ida E. Holm; et al.

  Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: Consensus recommendations

  Acta Neuropathologica. 2009;117(1):15-18.
  170

• 36.

  2009

  Ruben Vidal; Ana G. Barbeito; Leticia Miravalle; Bernardino Ghetti

  Cerebral amyloid angiopathy and parenchymal amyloid deposition in transgenic mice expressing the Danish mutant form of human BRI₂

  Brain Pathology. 2009;19(1):58-68.
  17

• 37.

  2009

  Xiangzhu Xiao; Leticia Miravalle; Jue Yuan; John McGeehan; Zhiqian Dong; Robert Wyza; Gregory T. MacLennan; Alan M. Golichowski; Geoff Kneale; Nicholas King; et al.

  Failure to detect the presence of prions in the uterine and gestational tissues from a gravida with Creutzfeldt-Jakob disease

  American Journal of Pathology. 2009;174(5):1602-1608.
  5

• 38.

  2009

  Ana G. Barbeito; Holly J. Garringer; Martin A. Baraibar; Xiaoying Gao; Miguel Arredondo; Marco T. Núñez; Mark A. Smith; Bernardino Ghetti; Ruben Vidal

  Abnormal iron metabolism and oxidative stress in mice expressing a mutant form of the ferritin light polypeptide gene

  Journal of Neurochemistry. 2009;109(4):1067-1078.
  25

• 39.

  2009

  Luca Giliberto; Roberta Borghi; Alessandra Piccini; Rosa Mangerini; Sandro Sorbi; Gabriella Cirmena; Anna Garuti; Bernardino Ghetti; Fabrizio Tagliavini; Mohamed R. Mughal; et al.

  Mutant presenilin 1 increases the expression and activity of BACE1

  Journal of Biological Chemistry. 2009;284(14):9027-9038.
  23

• 40.

  2009

  Bernardino Ghetti

  Old age before cognitive impairment

  Current Alzheimer Research. 2009;6(4):323.
  1

• 41.

  2009

  Fabienne Ory-Magne; Christine Brefel-Courbon; Pierre Payoux; Sabrina Debruxelles; Igor Sibon; Cyril Goizet; Pierre Labauge; Patrice Menegon; Emmanuelle Uro-Coste; et al.

  Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498-499InsTC)

  Movement Disorders. 2009;24(11):1676-1683.
  6

• 42.

  2009

  Joaquín Martí; María C. Santa-Cruz; Vanessa Molina; Roger Serra; Shirley A. Bayer; Bernardino Ghetti; José P. Hervás

  Regional differences in the vulnerability of substantia nigra dopaminergic neurons in weaver mice

  Acta Neurobiologiae Experimentalis. 2009;69(2):198-206.
  1

• 43.

  2009

  Edward D. Huey; Matteo Pardini; Alyson Cavanagh; Eric M. Wassermann; Dimitrios Kapogiannis; Salvatore Spina; Bernardino Ghetti; Jordan Grafman

  Association of ideomotor apraxia with frontal gray matter volume loss in corticobasal syndrome

  Archives of Neurology. 2009;66(10):1274-1280.
  4

• 44.

  2009

  Gabor G. Kovacs; Jill R. Murrell; Sandor Horvath; Laszlo Haraszti; Katalin Majtenyi; Maria J. Molnar; Herbert Budka; Bernardino Ghetti; Salvatore Spina

  TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea

  Movement Disorders. 2009;24(12):1843-1847.
  61

• 45.

  2009

  Piero Parchi; Rosaria Strammiello; Silvio Notari; Armin Giese; Jan P. M. Langeveld; Anna Ladogana; Inga Zerr; Federico Roncaroli; Patrich Cras; Bernardino Ghetti; et al.

  Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrP^Sc types: An updated classification

  Acta Neuropathologica. 2009;118(5):659-671.
  41

• 46.

  2009

  Steffen Albrecht; Nenad Bogdanovic; Bernardino Ghetti; Bengt Winblad; Andréa C. Leblanc

  Caspase-6 activation in familial alzheimer disease brains carrying amyloid precursor protein or presenilin i or presenilin II mutations

  Journal of Neuropathology and Experimental Neurology. 2009;68(12):1282-1293.
  16

• 47.

  2008

  Salvatore Spina; Martin R. Farlow; Frederick W. Unverzagt; David A. Kareken; Jill R. Murrell; Graham Fraser; Francine Epperson; R. Anthony Crowther; Maria G. Spillantini; et al.

  The tauopathy associated with mutation +3 in intron 10 of Tau: Characterization of the MSTD family

  Brain. 2008;131(1):72-89.
  12

• 48.

  2008

  Ruben Vidal; Leticia Miravalle; Xiaoying Gao; Ana G. Barbeito; Martin A. Baraibar; Shahryar K. Hekmatyar; Mario Widel; Navin Bansal; Marie B. Delisle; Bernardino Ghetti

  Expression of a mutant form of the ferritin light chain gene induces neurodegeneration and iron overload in transgenic mice

  Journal of Neuroscience. 2008;28(1):60-67.
  35

• 49.

  2008

  Patrice Delobel; Isabelle Lavenir; Graham Fraser; Esther Ingram; Max Holzer; Bernardino Ghetti; Maria Grazia Spillantini; R. Anthony Crowther; Michel Goedert

  Analysis of tau phosphorylation and truncation in a mouse model of human tauopathy

  American Journal of Pathology. 2008;172(1):123-131.
  39

• 50.

  2008

  Ana Velasco; Graham Fraser; Patrice Delobel; Bernardino Ghetti; Isabelle Lavenir; Michel Goedert

  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):901-906.
  12

• 51.

  2008

  Bernardino Ghetti; Salvatore Spina; Jill R. Murrell; Edward D. Huey; Pietro Pietrini; Brian Sweeney; Eric M. Wassermann; Catherine Keohane; Martin R. Farlow; et al.

  In vivo and postmortem clinicoanatomical correlations in frontotemporal dementia and parkinsonism linked to chromosome 17

  Neurodegenerative Diseases. 2008;5(3-4):215-217.
  9

• 52.

  2008

  Gregory D. Van Vickle; Chera L. Esh; Tyler A. Kokjohn; R. Lyle Patton; Walter M. Kalback; Dean C. Luehrs; Thomas G. Beach; Amanda J. Newel; Francisco Lopera; Bernardino Ghetti; et al.

  Presenilin-1 280Glu→ala mutation alters C-terminal APP processing yielding longer Aβ peptides: Implications for Alzheimer's disease

  Molecular Medicine. 2008;14(3-4):184-194.
  7

• 53.

  2008

  Gabor G. Kovacs; Katalin Majtenyi; Salvatore Spina; Jill R. Murrell; Ellen Gelpi; Romana Hoftberger; Graham Fraser; R. Anthony Crowther; Michel Goedert; Herbert Budka; et al.

  White matter tauopathy with globular glial inclusions: A distinct sporadic frontotemporal lobar segeneration

  Journal of Neuropathology and Experimental Neurology. 2008;67(10):963-975.
  23

• 54.

  2008

  Chera L. Maarouf; Ian D. Daugs; Salvatore Spina; Ruben Vidal; Tyler A. Kokjohn; R. Lyle Patton; Walter M. Kalback; Dean C. Luehrs; Douglas G. Walker; et al.

  Histopathological and molecular heterogeneity among individuals with dementia associated with Presenilin mutations

  Molecular Neurodegeneration. 2008;3(1).
  13

• 55.

  2008

  Silvio Notari; Rosaria Strammiello; Sabina Capellari; Armin Giese; Maura Cescatti; Jacques Grassi; Bernardino Ghetti; Jan P. M. Langeveld; Wen-Quan Zou; Pierluigi Gambetti; et al.

  Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease

  Journal of Biological Chemistry. 2008;283(45):30557-30565.
  30

• 56.

  2008

  Roberto Chiesa; Pedro Piccardo; Emiliano Biasini; Bernardino Ghetti; David A. Harris

  Aggregated, wild-type prion protein causes neurological dysfunction and synaptic abnormalities

  Journal of Neuroscience. 2008;28(49):13258-13267.
  21

• 57.

  2007

  Giuseppe Di Fede; Giorgio Giaccone; Lucia Limido; Michela Mangieri; Silvia Suardi; Gianfranco Puoti; Michela Morbin; Giulia Mazzoleni; Bernardino Ghetti; Fabrizio Tagliavini

  The ε 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):124-130.
  5

• 58.

  2007

  Michel Goedert; Bernardino Ghetti

  Alois Alzheimer: His life and times

  Brain Pathology. 2007;17(1):57-62.
  12

• 59.

  2007

  Bernardino Ghetti; Michel Goedert

  Symposium: Tau protein and neurodegeneration

  Brain Pathology. 2007;17(1):56.
  0

• 60.

  2007

  John M. Ringman; Yaneth Rodriguez; Claudia Diaz-Olavarrieta; Mireya Chavez; Michael Thompson; Lynn Fairbanks; Francisco Paz; Arousiak Varpetian; Hector Chaparro; Miguel Angel Macias-Islas; et al.

  Performance on MMSE sub-items and education level in presenilin-1 mutation carriers without dementia

  International Psychogeriatrics. 2007;19(2):323-332.
  1

• 61.

  2007

  Salvatore Spina; Jill R. Murrell; Hirotaka Yoshida; Bernardino Ghetti; Niamh Bermingham; Brian Sweeney; Stephen R. Dlouhy; R. Anthony Crowther; Michel Goedert; et al.

  The novel Tau mutation G335S: Clinical, neuropathological and molecular characterization

  Acta Neuropathologica. 2007;113(4):461-470.
  5

• 62.

  2007

  S. Spina; J.R. Murrell; E.D. Huey; E.M. Wassermann; P. Pietrini; M.A. Baraibar; A.G. Barbeito; J.C. Troncoso; R. Vidal; B. Ghetti; et al.

  Clinicopathologic features of frontotemporal dementia with Progranulin sequence variation

  Neurology. 2007;68(11):820-827.
  48

• 63.

  2007

  Pedro Piccardo; Jean C. Manson; Declan King; Bernardino Ghetti; Rona M. Barron

  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):4712-4717.
  61

• 64.

  2007

  Alessandra Piccini; Gianluigi Zanusso; Roberta Borghi; Cristiana Noviello; Salvatore Monaco; Roberta Russo; Gianluca Damonte; Andrea Armirotti; Matteo Gelati; Renzo Giordano; et al.

  Association of a presenilin 1 S170F mutation with a novel Alzheimer disease molecular phenotype

  Archives of Neurology. 2007;64(5):738-745.
  29

• 65.

  2007

  Aimin Li; Pedro Piccardo; Sami J. Barmada; Bernardino Ghetti; David A. Harris

  Prion protein with an octapeptide insertion has impaired neuroprotective activity in transgenic mice

  EMBO Journal. 2007;26(11):2777-2785.
  20

• 66.

  2007

  Y. Baba; M.C. Baker; I. Le Ber; A. Brice; L. Maeck; J. Kohlhase; M. Yasuda; G. Stoppe; O. Bugiani; A.D. Sperfeld; et al.

  Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation

  Journal of Neural Transmission. 2007;114(7):947-950.
  7

• 67.

  2007

  Joaquín Martí; M.C. Santa-Cruz; Shirley A. Bayer; Bernardino Ghetti; José P. Hervás

  Generation and survival of midbrain dopaminergic neurons in weaver mice

  International Journal of Developmental Neuroscience. 2007;25(5):299-307.
  2

• 68.

  2007

  Duane L. Beekly; Erin M. Ramos; William W. Lee; Woodrow D. Deitrich; Mary E. Jacka; Joylee Wu; Janene L. Hubbard; Thomas D. Koepsell; John C. Morris; Walter A. Kukull; et al.

  The National Alzheimer's Coordinating Center (NACC) database: The uniform data set

  Alzheimer Disease and Associated Disorders. 2007;21(3):249-258.
  46

• 69.

  2007

  Rosa Rademakers; Matt Baker; Jennifer Gass; Jennifer Adamson; Edward D Huey; Parastoo Momeni; Salvatore Spina; Giovanni Coppola; Anna M Karydas; Heather Stewart; et al.

  Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation: an international initiative

  Lancet Neurology. 2007;6(10):857-868.
  81

• 70.

  2007

  Martin Ingelsson; Karunya Ramasamy; Carsten Russ; Stefanie H. Freeman; Jennifer Orne; Susan Raju; Toshifumi Matsui; John H. Growdon; Matthew P. Frosch; et al.

  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):471-479.
  10

• 71.

  2007

  Salvatore Spina; Jill R. Murrell; Edward D. Huey; Eric M. Wassermann; Pietro Pietrini; Jordan Grafman; Bernardino Ghetti

  Corticobasal syndrome associated with the A9D Progranulin mutation

  Journal of Neuropathology and Experimental Neurology. 2007;66(10):892-900.
  37

• 72.

  2007

  Joaquín Martí; M.C. Santa-Cruz; Shirley A. Bayer; Bernardino Ghetti; José P. Hervás

  Purkinje cell age-distribution in fissures and in foliar crowns: A comparative study in the weaver cerebellum

  Brain Structure and Function. 2007;212(3-4):347-357.
  0

• 73.

  2007

  Christopher M. Filley; Yvonne D. Rollins; C. Alan Anderson; David B. Arciniegas; Katherine L. Howard; Jill R. Murrell; Philip J. Boyer; Belte K. Kleinschmidt-DeMasters; Bernardino Ghetti

  The genetics of very early onset Alzheimer disease

  Cognitive and Behavioral Neurology. 2007;20(3):149-156.
  13

• 74.

  2006

  Patrice Delobel; Isabelle Lavenir; Bernardino Ghetti; Max Holzer; Michel Goedert

  Cell-cycle markers in a transgenic mouse model of human tauopathy: Increased levels of cyclin-dependent kinase inhibitors p21Cip1 and p27Kip1

  American Journal of Pathology. 2006;168(3):878-887.
  19

• 75.

  2006

  Zbigniew K. Wszolek; Yoshio Tsuboi; Bernardino Ghetti; Stuart Pickering-Brown; Yasuhiko Baba; William P. Cheshire

  Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)

  Orphanet Journal of Rare Diseases. 2006;1(1).
  20

• 76.

  2006

  Yasuhiko Baba; Bernardino Ghetti; Matthew C. Baker; Ryan J. Uitti; Michael L. Hutton; Keiji Yamaguchi; Thomas Bird; Wenlang Lin; Michael W. DeLucia; et al.

  Hereditary diffuse leukoencephalopathy with spheroids: Clinical, pathologic and genetic studies of a new kindred

  Acta Neuropathologica. 2006;111(4):300-311.
  25

• 77.

  2006

  George K. Tofaris; Pablo Garcia Reitböck; Trevor Humby; Sarah L. Lambourne; Mark O'Connell; Bernardino Ghetti; Helen Gossage; Piers C. Emson; Lawrence S. Wilkinson; Michel Goedert; et al.

  Pathological changes in dopaminergic nerve cells of the substantia nigra and olfactory bulb in mice transgenic for truncated human α-synuclein(1- 120): Implications for lewy body disorders

  Journal of Neuroscience. 2006;26(15):3942-3950.
  101

• 78.

  2006

  A.-M. Shiarli; R. Jennings; J. Shi; K. Bailey; Y. Davidson; J. Tian; E.H. Bigio; B. Ghetti; J.R. Murrell; M.B. Delisle; et al.

  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):374-387.
  9

• 79.

  2006

  Kelly Schweitzer; Emily Decker; Liping Zhu; Richard E. Miller; Suzanne S. Mirra; Salvatore Spina; Bernardino Ghetti; Mu Wang; Jill Murrell

  Aberrantly regulated proteins in frontotemporal dementia

  Biochemical and Biophysical Research Communications. 2006;348(2):465-472.
  5

• 80.

  2006

  Gianluca Moroncini; Michela Mangieri; Michela Morbin; Giulia Mazzoleni; Bernardino Ghetti; Armando Gabrielli; Robert Anthony Williamson; Giorgio Giaccone; Fabrizio Tagliavini

  Pathologic prion protein is specifically recognized in situ by a novel PrP conformational antibody

  Neurobiology of Disease. 2006;23(3):717-724.
  16

• 81.

  2006

  Maria Grazia Spillantini; Jill R. Murrell; Michel Goedert; Martin Farlow; Aaron Klug; Bernardino Ghetti

  Mutations in the tau gene (MAPT) in FTDP-17: The family with Multiple System Tauopathy with Presenile Dementia (MSTD)

  Journal of Alzheimer's Disease. 2006;9(SUPPL. 3):373-380.
  5

• 82.

  2006

  Bernardino Ghetti

  Neurodegeneration and hereditary dementias: 40 Years of learning

  Journal of Alzheimer's Disease. 2006;9(SUPPL. 3):45-52.
  0

• 83.

  2006

  Bernardino Ghetti; Hans H. Goebel

  Frontotemporal dementia: The post-tau era

  Neurology. 2006;67(4):560-561.
  1

• 84.

  2006

  Monica Colucci; Francisco J. Moleres; Zhi-Liang Xie; Abhik Ray-Chaudhury; Sujata Gutti; Cathrin M. Butefisch; Larisa Cervenakova; Wen Wang; Lev G. Goldfarb; Qingzhong Kong; et al.

  Gerstmann-Sträussler-Scheinker: A new phenotype with 'curly' PrP deposits

  Journal of Neuropathology and Experimental Neurology. 2006;65(7):642-651.
  16

• 85.

  2006

  Rebecca Radde; Tristan Bolmont; Stephan A. Kaeser; Janaky Coomaraswamy; Dennis Lindau; Lars Stoltze; Michael E. Calhoun; Fabienne Jäggi; Hartwig Wolburg; et al.

  Aβ42-driven cerebral amyloidosis in transgenic mice reveals early and robust pathology

  EMBO Reports. 2006;7(9):940-946.
  110

• 86.

  2006

  Edward D. Huey; Jordan Grafman; Eric M. Wassermann; Pietro Pietrini; Michael C. Tierney; Bernardino Ghetti; Salvatore Spina; Matt Baker; Mike Hutton; et al.

  Characteristics of frontotemporal dementia patients with a Progranulin mutation

  Annals of Neurology. 2006;60(3):374-380.
  45

• 87.

  2006

  Jill Murrell; Bernardino Ghetti; Elizabeth Cochran; Miguel Angel Macias-Islas; Luis Medina; Arousiak Varpetian; Jeffrey L. Cummings; Mario F. Mendez; Claudia Kawas; Helena Chui; et al.

  The A431E mutation in PSEN1 causing Familial Alzheimer's Disease originating in Jalisco State, Mexico: An additional fifteen families

  Neurogenetics. 2006;7(4):277-279.
  21

• 88.

  2005

  Bradley F. Boeve; Ivo W. Tremont-Lukats; Andrew J. Waclawik; Jill R. Murrell; Bruce Hermann; Clifford R. Jack Jr.; Maria M. Shiung; Glenn E. Smith; Anil R. Nair; et al.

  Longitudinal characterization of two siblings with frontotemporal dementia and parkinsonism linked to chromosome 17 associated with the S305N tau mutation

  Brain. 2005;128(4):752-772.
  28

• 89.

  2005

  Yasuhiko Baba; Yoshio Tsuboi; Matthew C. Baker; Ryan J. Uitti; Michael L. Hutton; Dennis W. Dickson; Matthew Farrer; John D. Putzke; Bryan K. Woodruff; Bernardino Ghetti; et al.

  The Effect of tau genotype on clinical features in FTDP-17

  Parkinsonism and Related Disorders. 2005;11(4):205-208.
  19

• 90.

  2005

  Leticia Miravalle; Miguel Calero; Masaki Takao; Alex E. Roher; Bernardino Ghetti; Ruben Vidal

  Amino-terminally truncated Aβ peptide species are the main component of cotton wool plaques

  Biochemistry. 2005;44(32):10810-10821.
  60

• 91.

  2005

  J.M. Ringman; C. Diaz-Olavarrieta; Y. Rodriguez; M. Chavez; L. Fairbanks; F. Paz; A. Varpetian; H.C. Maldonado; M.A. Macias-Islas; et al.

  Neuropsychological function in nondemented carriers of presenilin-1 mutations

  Neurology. 2005;65(4):552-558.
  12

• 92.

  2005

  Rudy J. Castellani; Sandra L. Siedlak; Anne E. Fortino; George Perry; Bernardino Ghetti; Mark A. Smith

  Chitin-like polysaccharides in Alzheimer's disease brains

  Current Alzheimer Research. 2005;2(4):419-423.
  9

• 93.

  2005

  Keiji Yamaguchi; Elizabeth J. Cochran; Jill R. Murrell; Mihael H. Polymeropoulos; Kathleen M. Shannon; R. Anthony Crowther; Michel Goedert; Bernardino Ghetti

  Abundant neuritic inclusions and microvacuolar changes in a case of diffuse Lewy body disease with the A53T mutation in the α-synuclein gene

  Acta Neuropathologica. 2005;110(3):298-305.
  20

• 94.

  2005

  Robert B. Petersen; Sandra L. Siedlak; Hyoung-Gon Lee; Yong-Sun Kim; Akihiko Nunomura; Fabrizio Tagliavini; Bernardino Ghetti; Patrick Cras; Paula I. Moreira; Rudy J. Castellani; et al.

  Redox metals and oxidative abnormalities in human prion diseases

  Acta Neuropathologica. 2005;110(3):232-238.
  39

• 95.

  2005

  Chera Esh; Lyle Patton; Walter Kalback; Tyler A. Kokjohn; John Lopez; Daniel Brune; Amanda J. Newell; Thomas Beach; Dale Schenk; et al.

  Altered APP processing in PDAPP (Val717 → Phe) transgenic mice yields extended-length Aβ peptides

  Biochemistry. 2005;44(42):13807-13819.
  21

• 96.

  2005

  Roberto Chiesa; Pedro Piccardo; Sara Dossena; Lisa Nowoslawski; Kevin A. Roth; Bernardino Ghetti; David A. Harris

  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):238-243.
  52

• 97.

  2005

  A. Gemignani; P. Pietrini; J.R. Murrell; B.S. Glazier; P. Zolo; M. Guazzelli; B. Ghetti

  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.
  4

• 98.

  2005

  Richard S. Stewart; Pedro Piccardo; Bernardino Ghetti; David A. Harris

  Neurodegenerative illness in transgenic mice expressing a transmembrane form of the prion protein

  Journal of Neuroscience. 2005;25(13):3469-3477.
  38

• 99.

  2005

  Syed I.A. Zaidi; Sandra L. Richardson; Sabina Capellari; Li Song; Mark A. Smith; Bernardino Ghetti; Man-Sun Sy; Pierluigi Gambetti; Robert B. Petersen

  Characterization of the F198S prion protein mutation: Enhanced glycosylation and defective refolding

  Journal of Alzheimer's Disease. 2005;7(2):159-171.
  9

• 100.

  2005

  Bernardino Ghetti

  Recognition: Robert Terry

  Alzheimer's and Dementia. 2005;1(1):78.
  0

• 101.

  2004

  Ruben Vidal; Bernardino Ghetti; M. Takao; C. Brefel-Courbon; E. Uro-Coste; B.S. Glazier; V. Siani; M.D. Benson; P. Calvas; L. Miravalle; et al.

  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):363-380.
  71

• 102.

  2004

  Alex E. Roher; Tyler A. Kokjohn; Chera Esh; Nicole Weiss; Jennifer Childress; Walter Kalback; Dean C. Luehrs; John Lopez; Daniel Brune; Yu-Min Kuo; et al.

  The Human Amyloid-β Precursor Protein₇₇₀ Mutation V717F Generates Peptides Longer Than Amyloid-β-(40-42) and Flocculent Amyloid Aggregates

  Journal of Biological Chemistry. 2004;279(7):5829-5836.
  17

• 103.

  2004

  Antonella Vitali; Alessandra Piccini; Roberta Borghi; Pantaleo Fornaro; Sandra L. Siedlak; Mark A. Smith; Pierluigi Gambetti; Bernardino Ghetti; Massimo Tabaton

  Soluble amyloid β-protein is increased in frontotemporal dementia with tau gene mutations

  Journal of Alzheimer's Disease. 2004;6(1):45-51.
  9

• 104.

  2004

  Silvio Notari; Sabina Capellari; Armin Giese; Ingo Westner; Agostino Baruzzi; Bernardino Ghetti; Pierluigi Gambetti; Hans A. Kretzschmar; Piero Parchi

  Effects of different experimental conditions on the PrP^Sc core generated by protease digestion: Implications for strain typing and molecular classification of CJD

  Journal of Biological Chemistry. 2004;279(16):16797-16804.
  69

• 105.

  2004

  Masaki Takao; Bernardino Ghetti; Hirotaka Yoshida; Pedro Piccardo; Yolanda Narain; Jill R. Murrell; Ruben Vidal; Bradley S. Glazier; Ross Jakes; et al.

  Early-onset dementia with Lewy bodies

  Brain Pathology. 2004;14(2):137-147.
  15

• 106.

  2004

  Sami Barmada; Pedro Piccardo; Keiji Yamaguchi; Bernardino Ghetti; David A. Harris

  GFP-tagged prion protein is correctly localized and functionally active in the brains of transgenic mice

  Neurobiology of Disease. 2004;16(3):527-537.
  35

• 107.

  2004

  Ruben Vidal; Marie Bernadette Delisle; Bernardino Ghetti

  Neurodegeneration caused by proteins with an aberrant carboxyl-terminus

  Journal of Neuropathology and Experimental Neurology. 2004;63(8):787-800.
  22

• 108.

  2004

  Bryan K. Woodruff; Yasuhiko Baba; Michael L. Hutton; Zbigniew K. Wszolek; Yoshio Tsuboi; Tomonori Kobayashi; Bernardino Ghetti; Kunimasa Arima; Minoru Yasuda; Olivier Rascol; et al.

  Haplotype-phenotype correlations in kindreds with the N279K mutation in the tau gene [1] (multiple letters)

  Archives of Neurology. 2004;61(8):1327.
  0

• 109.

  2003

  David A. Harris; Roberto Chiesa; Bettina Drisaldi; Elena Quaglioa; Antonio Migheli; Pedro Piccardo; Bernardino Ghetti

  A murine model of a familial prion disease

  Clinics in Laboratory Medicine. 2003;23(1):175-186.
  6

• 110.

  2003

  James M. Powers; N.P. Byrne; M. Ito; M. Takao; D. Yankopoulou; M.G. Spillantini; B. Ghetti

  A novel leukoencephalopathy associated with tau deposits primarily in white matter glia

  Acta Neuropathologica. 2003;106(2):181-187.
  13

• 111.

  2003

  Roberto Chiesa; Pedro Piccardo; Elena Quaglio; Bettina Drisaldi; San Ling Si-Hoe; Masaki Takao; Bernardino Ghetti; David A. Harris

  Molecular distinction between pathogenic and infectious properties of the prion protein

  Journal of Virology. 2003;77(13):7611-7622.
  79

• 112.

  2003

  Giuseppe De Michele; Maurizio Pocchiari; Rossella Petraroli; Mario Manfredi; Giorgio Caneve; Giovanni Coppola; Carlo Casali; Francesco Saccà; Pedro Piccardo; et al.

  Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family

  Canadian Journal of Neurological Sciences. 2003;30(3):233-236.
  8

• 113.

  2003

  Bernardino Ghetti; Fabrizio Tagliavini; M. Takao; Orso Bugiani; Pedro Piccardo

  Hereditary prion protein amyloidoses

  Clinics in Laboratory Medicine. 2003;23(1):65-85.
  27

• 114.

  2003

  Bernardino Ghetti; Pedro Piccardo

  Prion diseases

  Clinics in Laboratory Medicine. 2003;23(1):xv-xvi.
  0

• 115.

  2003

  George K. Tofaris; Azam Razzaq; Bernardino Ghetti; Kathryn S. Lilley; Maria Grazia Spillantini

  Ubiquitination of α-Synuclein in Lewy Bodies Is a Pathological Event Not Associated with Impairment of Proteasome Function

  Journal of Biological Chemistry. 2003;278(45):44405-44411.
  127

• 116.

  2003

  Ruben Vidal; Marie Bernadette Delisle; Olivier Rascol; Bernardino Ghetti

  Hereditary ferritinopathy

  Journal of the Neurological Sciences. 2003;207(1-2):110-111.
  22

• 117.

  2002

  Joaquin Marti; Katherine V. Wills; Bernardino Ghetti; Shirley A. Bayer

  Regional differences in the Purkinje cells settled pattern: A comparative autoradiographic study in control and homozygous weaver mice

  Experimental Neurology. 2002;175(1):168-181.
  4

• 118.

  2002

  Yoshio Tsuboi; Ryan J. Uitti; Marie-Bernadette Delisle; Joaquim J. Ferreira; Christine Brefel-Courbon; Olivier Rascol; Bernardino Ghetti; Jill R. Murrell; Michael Hutton; Matthew Baker; et al.

  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):943-950.
  14

• 119.

  2002

  Joaquín Martí; Katherine V Wills; Bernardino Ghetti; Shirley A Bayer

  A combined immunohistochemical and autoradiographic method to detect midbrain dopaminergic neurons and determine their time of origin

  Brain Research Protocols. 2002;9(3):197-205.
  13

• 120.

  2002

  Adesola Ogunniyi; Effiong E. U. Akang; Oye Gureje; Masaki Takao; Pedro Piccardo; Olusegun Baiyewu; Kathleen S. Hall; Bernardino Ghetti; Hugh C. Hendrie

  Dementia with Lewy bodies in a Nigerian: A case report

  International Psychogeriatrics. 2002;14(2):211-218.
  8

• 121.

  2002

  Jin Zhong; Jixian Deng; Bernardino Ghetti; Wei-Hua Lee

  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.
  19

• 122.

  2002

  Bridget Allen; Esther Ingram; Masaki Takao; Michael J. Smith; Ross Jakes; Kanwar Virdee; Hirotaka Yoshida; Max Holzer; Molly Craxton; Piers C. Emson; et al.

  Abundant tau filaments and nonapoptotic neurodegeneration in transgenic mice expressing human P301s tau protein

  Journal of Neuroscience. 2002;22(21):9340-9351.
  209

• 123.

  2002

  Masaki Takao; Bernardino Ghetti; Isao Hayakawa; Eiji Ikeda; Yasuo Fukuuchi; Leticia Miravalle; Pedro Piccardo; Jill R. Murell; Bradley S. Glazier; Atsuo Koto

  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):155-170.
  34

• 124.

  2002

  Y. Tsuboi; M. Baker; M.L. Hutton; R.J. Uitti; O. Rascol; M.-B. Delisle; X. Soulages; J.R. Murrell; B. Ghetti; M. Yasuda; et al.

  Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)

  Neurology. 2002;59(11):1791-1793.
  20

• 125.

  2002

  Ana Lia Taratuto; P. Piccardo; E.G. Reich; S.G. Chen; G. Sevlever; M. Schultz; A.A. Luzzi; M. Rugiero; G. Abecasis; M. Endelman; et al.

  Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease

  Neurology. 2002;58(3):362-367.
  31

• 126.

  2002

  Emil Adamec; Jill R. Murrell; Masaki Takao; Wendy Hobbs; Ralph A. Nixon; Bernardino Ghetti; Jean P. Vonsattel

  P301L tauopathyconfocal immunofluorescence study of perinuclear aggregation of the mutated protein

  Journal of the Neurological Sciences. 2002;200(1-2):85-93.
  16

• 127.

  2002

  Richard L. Davis; Antony E. Shrimpton; Robin W. Carrell; David A. Lomas; Lieselotte Gerhard; Bruno Baumann; Daniel A. Lawrence; Manuel Yepes; Tai Seung Kim; Bernardino Ghetti; et al.

  Association between conformational mutations in neuroserpin and onset and severity of dementia

  Lancet. 2002;359(9325):2242-2247.
  72

• 128.

  2002

  Tobias Moehlmann; Edith Winkler; Xuefeng Xia; Dieter Edbauer; Jill Murrell; Anja Capell; Christoph Kaether; Hui Zheng; Bernardino Ghetti; Christian Haass; et al.

  Presenilin-1 mutations of leucine 166 equally affect the generation of the Notch and APP intracellular domains independent of their effect on Aβ₄₂ production

  Proceedings of the National Academy of Sciences of the United States of America. 2002;99(12):8025-8030.
  161

• 129.

  2001

  Anne Cataldo; G. William Rebeck; Bernadino Ghetti; Christine Hulette; Carol Lippa; Christine Van Broeckhoven; Cornelia Van Duijn; Patrick Cras; Nenad Bogdanovic; Thomas Bird; et al.

  Endocytic disturbances distinguish among subtypes of Alzheimer's disease and related disorders

  Annals of Neurology. 2001;50(5):661-665.
  30

• 130.

  2001

  Peter K. Panegyres; Kathrine Toufexis; B.A. Kakulas; Larisa Cernevakova; P. Brown; B. Ghetti; P. Piccardo; S.R. Dlouhy

  A new PRNP mutation (G131V) associated with Gerstmann-Sträussler-Scheinker disease

  Archives of Neurology. 2001;58(11):1899-1902.
  29

• 131.

  2001

  Joaquín Martí; Katherine V Wills; Bernardino Ghetti; Shirley A Bayer

  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. 2001;19(6):599-610.
  7

• 132.

  2001

  J.M. Ringman; V. Jain; J. Murrell; B. Ghetti; E.J. Cochran

  Gene symbol: PSEN1 Disease: Alzheimer disease

  Human Genetics. 2001;109(2):242.
  1

• 133.

  2001

  Pedro Piccardo; Juris J. Liepnieks; Albert William; Stephen R. Dlouhy; Martin R. Farlow; Katherine Young; David Nochlin; Thomas D. Bird; Randal R. Nixon; Melvyn J. Ball; et al.

  Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations

  American Journal of Pathology. 2001;158(6):2201-2207.
  37

• 134.

  2001

  R. Chiesa; A. Pestronk; R.E. Schmidt; W.G. Tourtellotte; B. Ghetti; P. Piccardo; D.A. Harris

  Primary myopathy and accumulation of PRP^Sc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutation

  Neurobiology of Disease. 2001;8(2):279-288.
  30

• 135.

  2001

  M. Yazaki; J.J. Liepnieks; J.R. Murrell; M. Takao; B. Guenther; P. Piccardo; M.R. Farlow; B. Ghetti; M.D. Benson

  Biochemical characterization of a neuroserpin variant associated with hereditary dementia

  American Journal of Pathology. 2001;158(1):227-233.
  19

• 136.

  2001

  Efrat Levy; Magdalena Sastre; Asok Kumar; Gloria Gallo; Pedro Piccardo; Bernardino Ghetti; Fabrizio Tagliavini

  Codeposition of cystatin C with amyloid-β protein in the brain of alzheimer disease patients

  Journal of Neuropathology and Experimental Neurology. 2001;60(1):94-104.
  90

• 137.

  2001

  Masaki Takao; Bernardino Ghetti; Jill R. Murrell; Frederick W. Unverzagt; Giorgio Giaccone; Fabrizio Tagliavini; Orso Bugiani; Pedro Piccardo; Christine M. Hulette; et al.

  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):1137-1152.
  28

• 138.

  2001

  Cristiana Atzori; Bernardino Ghetti; Roberto Piva; Anu N. Srinivasan; Paolo Zolo; Marie Bernadette Delisle; Suzanne S. Mirra; Antonio Migheli

  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):1190-1197.
  103

• 139.

  2001

  Fabrizio Tagliavini; Patricia M.-J. Lievens; Christine Tranchant; Jean-Marie Warter; Michel Mohr; Giorgio Giaccone; Francesco Perini; Giacomina Rossi; Mario Salmona; Pedro Piccardo; et al.

  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

  Journal of Biological Chemistry. 2001;276(8):6009-6015.
  73

• 140.

  2001

  D.A. Harris; R. Chiesa; B. Drisaldi; E. Quaglio; A. Migheli; P. Piccardo; B. Ghetti

  A transgenic model of a familial prion disease

  Archives of Virology, Supplement. 2001;(16):103-112.
  0

• 141.

  2000

  Piero Parchi; Wenquan Zou; Wen Wang; Paul Brown; Sabina Capellari; Bernardino Ghetti; Nicolas Kopp; Walter J. Schulz-Schaeffer; Hans A. Kretzschmar; Mark W. Head; et al.

  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):10168-10172.
  167

• 142.

  2000

  Marie-Bernadette Delisle; Emmanuelle Uro-Coste; J.R. Murrell; Olivier Rascol; Bernardino Ghetti

  Neurodegenerative disease with a mutation at codon 279 (N279 K) in exon 10 of the protein Tau gene

  Bulletin de l'Academie Nationale de Medecine. 2000;184(4):799-809.
  6

• 143.

  2000

  C. Russo; G. Schettini; T.C. Saido; C. Hulette; C. Lippa; L. Lannfelt; B. Ghetti; P. Gambetti; M. Tabaton; et al.

  Presenilin-1 mutations in Alzheimer's disease

  Nature. 2000;405(6786):531-532.
  99

• 144.

  2000

  C.F. Lippa; J.M. Swearer; K.J. Kane; D. Nochlin; T.D. Bird; B. Ghetti; L.E. Nee; P. St. George-Hyslop; D.A. Pollen; D.A. Drachman

  Familial Alzheimer's disease: Site of mutation influences clinical phenotype

  Annals of Neurology. 2000;48(3):376-379.
  37

• 145.

  2000

  Kimberly A. Quaid; Jill R. Murrell; Ann M. Hake; Martin R. Farlow; Bernardino Ghetti

  Presymptomatic genetic testing with an APP mutation in Early-onset Alzheimer disease: A descriptive study of sibship dynamics

  Journal of Genetic Counseling. 2000;9(4):327-341.
  6

• 146.

  2000

  Rubén Vidal; Miguel Calero; Pedro Piccardo; Martin R. Farlow; Frederick W. Unverzagt; Enrique Méndez; Adolfo Jiménez-Huete; Ronald Beavis; Gloria Gallo; et al.

  Senile dementia associated with amyloid β protein angiopathy and tau perivascular pathology but not neuritic plaques in patients homozygous for the APOE-ε4 allele

  Acta Neuropathologica. 2000;100(1):1-12.
  40

• 147.

  2000

  Jill R. Murrell; Ann M. Hake; Kimberly A. Quaid; Martin R. Farlow; Bernardino Ghetti

  Early-onset Alzheimer disease caused by a new mutation (V717L) in the amyloid precursor protein gene

  Archives of Neurology. 2000;57(6):885-887.
  31

• 148.

  2000

  Orso Bugiani; Giorgio Giaccone; Pedro Piccardo; Michela Morbin; Fabrizio Tagliavini; Bernardino Ghetti

  Neuropathology of Gerstmann-Straussler-Scheinker disease

  Microscopy Research and Technique. 2000;50(1):10-15.
  22

• 149.

  2000

  Sandro Sorbi; Margherita Alberoni; Pasquale Alfieri; Serena Amici; Daniele Antana; Ildebrando Appollonio; Stefano Avanzi; Antonella Bartoli; Bruno Bergamasco; Laura Bracco; et al.

  Guidelines for the diagnosis of dementia and Alzheimer's disease

  Neurological Sciences. 2000;21(4):187-194.
  34

• 150.

  2000

  Masaki Takao; Merril D. Benson; Jill R. Murrell; Masahide Yazaki; Pedro Piccardo; Frederick W. Unverzagt; Richard L. Davis; Peter D. Holohan; Daniel A. Lawrence; Rosemarie Richardson; et al.

  Neuroserpin mutation S52R causes Neuroserpin accumulation in neurons and is associated with progressive myoclonus epilepsy

  Journal of Neuropathology and Experimental Neurology. 2000;59(12):1070-1086.
  40

• 151.

  2000

  Michel Goedert; Bernardino Ghetti; Maria Grazia Spillantini

  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.
  31

• 152.

  2000

  Bernardino Ghetti; Jill R. Murrell; Paolo Zolo; Maria Grazia Spillantini; Michel Goedert

  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.
  16

• 153.

  2000

  D.A. Harris; R. Chiesa; B. Drisaldi; E. Quaglio; A. Migheli; P. Piccardo; B. Ghetti

  A transgenic model of a familial prion disease.

  Archives of virology. Supplementum. 2000;(16):103-112.
  2

• 154.

  2000

  Roberto Chiesa; Bettina Drisaldi; Elena Quaglio; Antonio Migheli; Pedro Piccardo; Bernardino Ghetti; David A. Harris

  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):5574-5579.
  93

• 155.

  2000

  A.B. Harkins; S. Dlouhy; B. Ghetti; A.L. Cahill; L. Won; B. Heller; A. Heller; A.P. Fox

  Evidence of elevated intracellular calcium levels in weaver homozygote mice

  Journal of Physiology. 2000;524(2):447-455.
  9

• 156.

  2000

  Joaquín Martí; Katherine V. Wills; Bernardino Ghetti; Shirley A. Bayer

  The weaver gene has no effect on the generation patterns of mesencephalic dopaminergic neurons

  Developmental Brain Research. 2000;122(2):165-172.
  6

• 157.

  2000

  Joaquín Martí; Katherine V. Wills; Bernardino Ghetti; Shirley A. Bayer

  The weaver gene continues to target late-generated dopaminergic neurons in midbrain areas at P90

  Developmental Brain Research. 2000;122(2):173-181.
  6

• 158.

  1999

  W. Zhang; B. Ghetti; X.-L. Yang; W.-H. Lee

  Alteration of IGF system gene expression during the postnatal development of pcd mice

  Journal of Endocrinology. 1999;163(2):191-198.
  8

• 159.

  1999

  Bernardino Ghetti; Jill Murrell; Maria Grazia Spillantini

  Mutations in the Tau gene cause frontotemporal dementia

  Brain Research Bulletin. 1999;50(5-6):471-472.
  5

• 160.

  1999

  Jill R. Murrell; Maria Grazia Spillantini; Paolo Zolo; Mario Guazzelli; Michael J. Smith; Masato Hasegawa; Francesco Redi; R. Anthony Crowther; Pietro Pietrini; Bernardino Ghetti; et al.

  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):1207-1226.
  144

• 161.

  1999

  Jeffrey D. Broome; Katherine V. Wills; Paul A. Lapchak; Bernardino Ghetti; Laurel L. Camp; Shirley A. Bayer

  Glial cell line-derived neurotrophic factor protects midbrain dopamine neurons from the lethal action of the weaver gene: A quantitative immunocytochemical study

  Developmental Brain Research. 1999;116(1):1-7.
  11

• 162.

  1999

  Antonio Migheli; Roberto Piva; Stefania Casolino; Cristiana Atzori; Stephen R. Dlouhy; Bernardino Ghetti

  A cell cycle alteration precedes apoptosis of granule cell precursors in the weaver mouse cerebellum

  American Journal of Pathology. 1999;155(2):365-373.
  43

• 163.

  1999

  Piero Parchi; Armin Giese; Sabina Capellari; Paul Brown; Walter Schulz-Schaeffer; Otto Windl; Inga Zerr; Herbert Budka; Nicolas Kopp; et al.

  Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

  Annals of Neurology. 1999;46(2):224-233.
  643

• 164.

  1999

  Suzanne S. Mirra; Jill R. Murrell; Marla Gearing; Maria G. Spillantini; Michel Goedert; R. Anthony Crowther; Allan I. Levey; Randi Jones; Joanne Green; John M. Shoffner; et al.

  Tau pathology in a family with dementia and a P301L mutation in tau

  Journal of Neuropathology and Experimental Neurology. 1999;58(4):335-345.
  108

• 165.

  1999

  Marie-Bernadette Delisle; Jill R. Murrell; Rosemarie Richardson; James A. Trofatter; Olivier Rascol; Xavier Soulages; Michel Mohr; Patrick Calvas; Bernardino Ghetti

  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.
  109

• 166.

  1999

  Orso Bugiani; Jill R. Murrell; Giorgio Giaccone; Masato Hasegawa; Giuseppe Ghigo; Massimo Tabaton; Michela Morbin; Alberto Primavera; Francesco Carella; et al.

  Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau

  Journal of Neuropathology and Experimental Neurology. 1999;58(6):667-677.
  207

• 167.

  1999

  L. Varani; M. Hasegawa; M.G. Spillantini; M.J. Smith; J.R. Murrell; B. Ghetti; A. Klug; M. Goedert; G. Varani

  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):8229-8234.
  140

• 168.

  1999

  Kelly R. Bales; Tatyana Verina; David J. Cummins; Yansheng Du; Richard C. Dodel; Josep Saura; Cindy E. Fishman; Cynthia A. Delong; Pedro Piccardo; et al.

  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):15233-15238.
  286

• 169.

  1999

  Bernardino Ghetti; Pierluigi Gambetti

  Chapter 5 Human Prion Diseases

  Advances in Cell Aging and Gerontology. 1999;3(C):135-187.
  0

• 170.

  1998

  Carol F. Lippa; Hideo Fujiwara; David M.A. Mann; Benoit Giasson; Minami Baba; Marie L. Schmidt; Linda E. Nee; Brendan O'Connell; Dan A. Pollen; Peter St. George-Hyslop; et al.

  Lewy bodies contain altered α-synuclein in brains of many familial Alzheimer's disease patients with mutations in presenilin and amyloid precursor protein genes

  American Journal of Pathology. 1998;153(5):1365-1370.
  284

• 171.

  1998

  Pedro Piccardo; Jan P. M. Langeveld; Andrew F. Hill; Stephen R. Dlouhy; Katherine Young; Giorgio Giaccone; Giacomina Rossi; Marianna Bugiani; Orso Bugiani; Rob H. Meloen; et al.

  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

  American Journal of Pathology. 1998;152(6):1415-1420.
  20

• 172.

  1998

  Paul Brown; L. Cervenáková; L. McShane; L.G. Goldfarb; K. Bishop; F. Bastian; J. Kirkpatrick; P. Piccardo; B. Ghetti; D.C. Gajdusek

  Creutzfeldt-Jakob disease in a husband and wife

  Neurology. 1998;50(3):684-688.
  21

• 173.

  1998

  V. Salanova; O. Markand; R. Worth; R. Smith; H. Wellman; G. Hutchins; H. Park; B. Ghetti; B. Azzarelli

  FDG-PET and MRI in temporal lobe epilepsy: Relationship to febrile seizures, hippocampal sclerosis and outcome

  Acta Neurologica Scandinavica. 1998;97(3):146-153.
  46

• 174.

  1998

  Pedro Piccardo; Stephen R. Dlouhy; Patricia M. J. Lievens; Katherine Young; Thomas D. Bird; David Nochlin; Dennis W. Dickson; Harry V. Vinters; Thomas R. Zimmerman; Ian R. A. Mackenzie; et al.

  Phenotypic variability of Gerstmann-Straussler-Scheinker disease is associated with prion protein heterogeneity

  Journal of Neuropathology and Experimental Neurology. 1998;57(10):979-988.
  104

• 175.

  1998

  A.P. Fox; S. Dlouhy; B. Ghetti; J.H. Hurley; P.G.P. Nucifora; D.J. Nelson; L. Won; A. Heller

  Altered responses to potassium in cerebellar neurons from weaver heterozygote mice

  Experimental Brain Research. 1998;123(3):298-306.
  6

• 176.

  1998

  Adolfo Jiménez-Huete; Patricia M. J. Lievens; Rubén Vidal; Pedro Piccardo; Bernardino Ghetti; Fabrizio Tagliavini; Blas Frangione; Frances Prelli

  Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissues

  American Journal of Pathology. 1998;153(5):1561-1572.
  117

• 177.

  1998

  Maria Grazia Spillantini; Thomas D. Bird; Bernardino Ghetti

  Frontotemporal dementia and Parkinsonism linked to chromosome 17: A new group of tauopathies

  Brain Pathology. 1998;8(2):387-402.
  282

• 178.

  1998

  Jianjun Wei; Marion E. Hodes; Roberto Piva; Yue Feng; Yi Wang; Bernardino Ghetti; Stephen R. Dlouhy

  Characterization of murine Girk2 transcript isoforms: Structure and differential expression

  Genomics. 1998;51(3):379-390.
  28

• 179.

  1998

  Neena B. Schwartz; Marta Szabo; Tatyana Verina; Jianjun Wei; Stephen R. Dlouhy; Lisa Won; Alfred Heller; Marion E. Hodes; Bernardino Ghetti

  Hypothalamic-pituitary-gonadal axis in the mutant weaver mouse

  Neuroendocrinology. 1998;68(6):374-385.
  12

• 180.

  1998

  Roberto Chiesa; Pedro Piccardo; Bernardino Ghetti; David A. Harris

  Neurological illness in transgenic mice expressing a prion protein with an insertional mutation

  Neuron. 1998;21(6):1339-1351.
  200

• 181.

  1998

  Maria Grazia Spillantini; Jill R. Murrell; Michel Goedert; Martin R. Farlow; Aaron Klug; Bernardino Ghetti

  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):7737-7741.
  873

• 182.

  1997

  Antonio Migheli; Roberto Piva; Jianjun Wei; Angelo Attanasio; Stefania Casolino; Marion E. Hodes; Stephen R. Dlouhy; Shirley A. Bayer; Bernardino Ghetti

  Diverse cell death pathways result from a single missense mutation in weaver mouse

  American Journal of Pathology. 1997;151(6):1629-1638.
  34

• 183.

  1997

  J.R. Murrell; D. Koller; T. Foroud; M. Goedert; M.G. Spillantini; H.J. Edenberg; M.R. Farlow; B. Ghetti

  Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17

  American Journal of Human Genetics. 1997;61(5):1131-1138.
  54

• 184.

  1997

  Maria Grazia Spillantini; Michel Goedert; R. Anthony Crowther; Jill R. Murrell; Martin R. Farlow; Bernardino Ghetti

  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):4113-4118.
  199

• 185.

  1997

  D.W. Park; H.C. Boldt; S.J. Massicotte; E.E.U. Akang; K.L. Roos; A. Bodnar; J. Pless; B. Ghetti; R.M. Pascuzzi

  Subacute sclerosing panencephalitis manifesting as viral retinitis: Clinical and histopathologic findings

  American Journal of Ophthalmology. 1997;123(4):533-542.
  21

• 186.

  1997

  Frederick W. Unverzagt; Martin R. Farlow; James Norton; Stephen R. Dlouhy; Katherine Young; Bernardino Ghetti

  Neuropsychological function in patients with Gerstmann-Straussler-Scheinker disease from the Indiana Kindred (F198S)

  Journal of the International Neuropsychological Society. 1997;3(2):169-178.
  8

• 187.

  1997

  J.R. Simon; D.J. Bare; B. Ghetti; J.A. Richter

  A possible role for tyrosine kinases in the regulation of the neuronal dopamine transporter in mouse striatum

  Neuroscience Letters. 1997;224(3):201-205.
  25

• 188.

  1997

  Lisa Won; Bernardino Ghetti; Barbara Heller; Alfred Heller

  In vitro evidence that the reduction in mesencepalic dopaminergic neurons in the weaver heterozygote is not due to a failure in target cell interaction

  Experimental Brain Research. 1997;115(1):174-179.
  5

• 189.

  1997

  Jianjun Wei; Stephen R. Dlouhy; Shirley Bayer; Roberto Piva; Tatyana Verina; Yi Wang; Yue Feng; Brenda Dupree; M.E. Hodes; Bernardino Ghetti

  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):762-771.
  22

• 190.

  1997

  Tatyana Verina; James A. Norton; Jeffrey J. Sorbel; Lazaros C. Triarhou; Donald Laferty; Judith A. Richter; Jay R. Simon; Bernardino Ghetti

  Atrophy and loss of dopaminergic mesencephalic neurons in heterozygous weaver mice

  Experimental Brain Research. 1997;113(1):5-12.
  12

• 191.

  1997

  Katherine Young; H. Brent Clark; Pedro Piccardo; Stephen R. Dlouhy; Bernardino Ghetti

  Gerstmann-Straussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129

  Molecular Brain Research. 1997;44(1):147-150.
  33

• 192.

  1997

  K.R. Bales; T. Verina; R.C. Dodel; Y. Du; L. Altstiel; M. Bender; P. Hyslop; E.M. Johnstone; S.P. Little; et al.

  Lack of apolipoprotein E dramatically reduces amyloid beta-peptide deposition.

  Nature genetics. 1997;17(3):263-264.
  498

• 193.

  1997

  Wei Zhang; Bernardino Ghetti; Wei-Hua Lee

  Decreased IGF-I gene expression during the apoptosis of Purkinje cells in pcd mice

  Developmental Brain Research. 1997;98(2):164-176.
  27

• 194.

  1996

  Wei Jianjun; Stephen R. Dlouhy; Akira Hara; Bernardino Ghetti; M.E. Hodes

  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):147-148.
  13

• 195.

  1996

  Bernardino Ghetti; Pedro Piccardo; Maria Grazia Spillantini; Yousuke Ichimiya; Monica Porro; Francesco Perini; Tetsuyuki Kitamoto; Jun Tateishi; Charles Seiler; Blas Frangione; et al.

  Vascular variant of prion protein cerebral amyloidosis with τ-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):744-748.
  150

• 196.

  1996

  Bernardino Ghetti; Pedro Piccardo; Blas Frangione; Orso Bugiani; Giorgio Giaccone; Katherine Young; Frances Prelli; Martin R. Farlow; Stephen R. Dlouhy; Fabrizio Tagliavini

  Prion protein amyloidosis

  Brain Pathology. 1996;6(2):127-145.
  116

• 197.

  1996

  Jianjun Wei; M.E. Hodes; Yi Wang; Yue Feng; Bernardino Ghetti; Stephen R. Dlouhy

  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):678-687.
  4

• 198.

  1996

  Jianjun Wei; Stephen R. Dlouhy; Yi Wang; Jianguo Zhu; Lillian Fitzpatrick; Bernardino Ghetti; M.E. Hodes

  Linkage mapping of microdissected clones from distal mouse chromosome 16

  Somatic Cell and Molecular Genetics. 1996;22(3):227-232.
  2

• 199.

  1996

  Bernardino Ghetti; Pedro Piccardo; Blas Frangione; Orso Bugiani; Giorgio Giaccone; Katherine Young; Frances Prelli; Martin R. Farlow; Stephen R. Dlouhy; et al.

  Prion protein hereditary amyloidosis: Parenchymal and vascular

  Seminars in Virology. 1996;7(3):189-200.
  8

• 200.

  1996

  Yanhe Tong; Jianjun Wei; Shengwen Zhang; Judith A. Strong; Stephen R. Dlouhy; M.E. Hodes; Bernardino Ghetti; Lei Yu

  The weaver mutation changes the ion selectivity of the affected inwardly rectifying potassium channel GIRK2

  FEBS Letters. 1996;390(1):63-68.
  44

• 201.

  1996

  Shirley A. Bayer; Katherine V. Wills; Jianjun Wei; Yue Feng; Stephen R. Dlouhy; Marion E. Hodes; Tatyana Verina; Bernardino Ghetti

  Phenotypic effects of the weaver gene are evident in the embryonic cerebellum but not in the ventral midbrain

  Developmental Brain Research. 1996;96(1-2):130-137.
  18

• 202.

  1996

  Francesco Perini; Ruben Vidal; Bernardino Ghetti; Fabrizio Tagliavini; Blas Frangione; Frances Prelli

  PRP_27-30 is a normal soluble prion protein fragment released by human platelets

  Biochemical and Biophysical Research Communications. 1996;223(3):572-577.
  56

• 203.

  1996

  Piero Parchi; Rudolph Castellani; Sabina Capellari; Bernardino Ghetti; Katherine Young; Shu G. Chen; Martin Farlow; Dennis W. Dickson; Anders A. F. Sima; John Q. Trojanowski; et al.

  Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

  Annals of Neurology. 1996;39(6):767-778.
  490

• 204.

  1996

  C.F. Lippa; A.M. Saunders; T.W. Smith; J.M. Swearer; D.A. Drachman; B. Ghetti; L. Nee; D. Pulaski-Salo; D. Dickson; Y. Robitaille; et al.

  Familial and sporadic Alzheimer's disease: Neuropathology cannot exclude a final common pathway

  Neurology. 1996;46(2):406-412.
  65

• 205.

  1996

  Pedro Piccardo; Charles Seiler; Stephen R. Dlouhy; Katherine Young; Martin R. Farlow; Frances Prelli; Blas Frangione; Orso Bugiani; Fabrizio Tagliavini; Bernardino Ghetti

  Proteinase-K-resistant prion protein isoforms in Gerstmann-Straussler- Scheinker disease (Indiana kindred)

  Journal of Neuropathology and Experimental Neurology. 1996;55(11):1157-1163.
  30

• 206.

  1995

  D.J. Bare; B. Ghetti; J.A. Richter

  The tyrosine kinase inhibitor genistein increases endogenous dopamine release from normal and weaver mutant mouse striatal slices

  Journal of Neurochemistry. 1995;65(5):2096-2104.
  4

• 207.

  1995

  L.C. Triarhou; C. Sola; G. Mengod; F.J. Garcia-Ladona; B. Landwehrmeyer; B. Ghetti; J.M. Palacios

  Ventral mesencephalic grafts in the neostriatum of the weaver mutant mouse: Structural molecule and receptor studies

  Cell Transplantation. 1995;4(1):39-48.
  4

• 208.

  1995

  Antonio Migheli; Angelo Attanasio; Wei-Hua Lee; Shirley A. Bayer; Bernardino Ghetti

  Detection of apoptosis in weaver cerebellum by electron microscopic in situ end-labeling of fragmented DNA

  Neuroscience Letters. 1995;199(1):53-56.
  48

• 209.

  1995

  J.A. Richter; D.J. Bare; H. Yu; B. Ghetti; J.R. Simon

  Dopamine transporter-dependent and -independent endogenous dopamine release from weaver mouse striatum in vitro

  Journal of Neurochemistry. 1995;64(1):191-198.
  10

• 210.

  1995

  K. Suzuki; C.C. Parker; P.G. Pentchev; D. Katz; B. Ghetti; A.N. D'Agostino; E.D. Carstea

  Neurofibrillary tangles in Niemann-Pick disease type C

  Acta Neuropathologica. 1995;89(3):227-238.
  104

• 211.

  1995

  P. Piccardo; B. Ghetti; D.W. Dickson; H.V. Vinters; G. Giaccone; O. Bugiani; F. Tagliavini; K. Young; S.R. Dlouhy; C. Seiler; et al.

  Gerstmann-Straussler-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.
  26

• 212.

  1995

  B. Ghetti; S.R. Dlouhy; G. Giaccone; O. Bugiani; B. Frangione; M.R. Farlow; F. Tagliavini

  Gerstmann-Straussler-Scheinker disease and the Indiana kindred

  Brain Pathology. 1995;5(1):61-75.
  87

• 213.

  1995

  K. Young; C.K. Jones; P. Piccardo; A. Lazzarini; L.I. Golbe; T.R. Zimmerman Jr.; D.W. Dickson; D.C. McLachlan; P. St. George-Hyslop; A. Lennox; et al.

  Gerstmann-Straussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients

  Neurology. 1995;45(6):1127-1134.
  38

• 214.

  1995

  J.A. Richter; M.G. Brenneman; S.R. Dlouhy; B. Ghetti

  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.
  1

• 215.

  1995

  Shirley A. Bayer; Katherine V. Wills; Lazaros C. Triarhou; Tatyana Verina; James D. Thomas; Bernardino Ghetti

  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):9137-9140.
  31

• 216.

  1995

  Wei-Hua Lee; Guo-Ming Wang; Teresa Lo; Lazaros C. Triarhou; Bernardino Ghetti

  Altered IGFBP5 gene expression in the cerebellar external germinal layer of weaver mutant mice

  Molecular Brain Research. 1995;30(2):259-268.
  16

• 217.

  1995

  E.H. Stotz-Potter; B. Ghetti; J.R. Simon

  Endogenous serotonin release from the dopamine-deficient striatum of the weaver mutant mouse

  Neurochemical Research. 1995;20(7):821-826.
  1

• 218.

  1995

  S.A. Bayer; K.V. Wills; L.C. Triarhou; B. Ghetti

  Time of neuron origin and gradients of neurogenesis in midbrain dopaminergic neurons in the mouse

  Experimental Brain Research. 1995;105(2):191-199.
  82

• 219.

  1995

  S.A. Bayer; K.V. Wills; L.C. Triarhou; J.D. Thomas; B. Ghetti

  Systematic differences in time of dopaminergic neuron origin between normal mice and homozygous weaver mutants

  Experimental Brain Research. 1995;105(2):200-208.
  17

• 220.

  1995

  T. Verina; X. Tang; L. Fitzpatrick; J. Norton; C. Vogelweid; B. Ghetti

  Degeneration of Sertoli and spermatogenic cells in homozygous and heterozygous weaver mice

  Journal of Neurogenetics. 1995;9(4):251-265.
  15

• 221.

  1994

  M.E. Hodes; S.R. Dlouhy; J.J. Wei; Y. Wang; L. Sangameswaran; V. Lazar; L.C. Triarhou; B. Ghetti

  cDNA approaches to isolation of the mouse mutant weaver gene

  Neurochemical Research. 1994;19(11):1359-1362.
  1

• 222.

  1994

  Shirley A. Bayer; Lazaros C. Triarhou; James D. Thomas; Bernardino Ghetti

  Correlated quantitative studies of the neostriatum, nucleus accumbens, substantia nigra, and ventral tegmental area in normal and weaver mutant mice

  Journal of Neuroscience. 1994;14(11 II):6901-6910.
  13

• 223.

  1994

  F. Tagliavini; F. Prelli; M. Porro; G. Rossi; G. Giaccone; M.R. Farlow; S.R. Dlouhy; B. Ghetti; O. Bugiani; B. Frangione

  Amyloid fibrils in Gerstmann-Straussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele

  Cell. 1994;79(4):695-703.
  101

• 224.

  1994

  M. Farlow; J. Murrell; B. Ghetti; F. Unverzagt; S. Zeldenrust; M. Benson

  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):105-111.
  20

• 225.

  1994

  J.R. Simon; J.A. Richter; B. Ghetti

  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):543-548.
  13

• 226.

  1994

  L.C. Triarhou; E.H. Stotz; W.C. Low; J. Norton; B. Ghetti; B. Landwehrmeyer; J.M. Palacios; J.R. Simon

  Studies on the striatal dopamine uptake system of weaver mutant mice and effects of ventral mesencephalic grafts

  Neurochemical Research. 1994;19(11):1349-1358.
  2

• 227.

  1994

  M. Farlow; B. Ghetti; S. Dlouhy; G. Giaccone; O. Bugiani; F. Tagliavini; S. Wagner

  Cerebrospinal fluid levels of amyloid β-protein precursor are low in Gerstmann-Straussler-Scheinker disease, Indiana kindred

  Neurology. 1994;44(8):1508-1510.
  2

• 228.

  1994

  M. Kambouris; L.C. Triarhou; S.R. Dlouhy; L. Sangameswaran; F. Luo; B. Ghetti; M.E. Hodes

  Novel cDNA clones obtained by antibody screening of a mouse cerebellar cDNA expression library

  Molecular Brain Research. 1994;25(3-4):183-191.
  3

• 229.

  1994

  E.H. Stotz; J.M. Palacios; B. Landwehrmeyer; J. Norton; B. Ghetti; J.R. Simon; L.C. Triarhou

  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.
  15

• 230.

  1994

  Lucia Monari; Shu G. Chen; Paul Brown; Piero Parchi; Robert B. Petersen; Jacqueline Mikol; Franscoise Gray; Pietro Cortelli; Pasquale Montagna; et al.

  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):2839-2842.
  189

• 231.

  1994

  Bernardino Ghetti; F. Tagliavini; G. Giaccone; O. Bugiani; Blas Frangione; M.R. Farlow; S.R. Dlouhy

  Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles

  Molecular Neurobiology. 1994;8(1):41-48.
  38

• 232.

  1994

  J.R. Simon; B. Ghetti

  The weaver mutant mouse as a model of nigrostriatal dysfunction

  Molecular Neurobiology. 1994;9(1-3):183-189.
  14

• 233.

  1994

  Jianjun Wei; Stephen R. Dlouhy; Jianguo Zhu; Bernardino Ghetti; M.E. Hodes

  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):401-408.
  7

• 234.

  1993

  J.R. Simon; B. Ghetti

  Is there a significant somatodendritic uptake of dopamine in the substantia nigra? Evidence from the weaver mutant mouse

  Neurochemistry International. 1993;22(5):471-477.
  9

• 235.

  1993

  F. Tagliavini; G. Giaccone; F. Prelli; L. Verga; M. Porro; J.Q. Trojanowski; M.R. Farlow; B. Frangione; B. Ghetti; O. Bugiani

  A68 is a component of paired helical filaments of Gerstmann-Straussler-Scheinker disease, Indiana kindred

  Brain Research. 1993;616(1-2):325-328.
  28

• 236.

  1993

  S.R. Zeldenrust; J. Murrell; M. Farlow; B. Ghetti; A.D. Roses; M.D. Benson

  RFLP analysis for APP 717 mutations associated with Alzheimer's disease

  Journal of Medical Genetics. 1993;30(6):476-478.
  5

• 237.

  1993

  M. Kambouris; L. Sangameswaran; S.R. Dlouhy; M.E. Hodes; B. Ghetti; L.C. Triarhou

  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

  Molecular Brain Research. 1993;18(4):321-328.
  2

• 238.

  1993

  F. Tagliavini; F. Prelli; L. Verga; G. Giaccone; R. Sarma; P. Gorevic; B. Ghetti; F. Passerini; E. Ghibaudi; G. Forloni; et al.

  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):9678-9682.
  168

• 239.

  1993

  E.H. Stotz; L.C. Triarhou; B. Ghetti; J.R. Simon

  Serotonin content is elevated in the dopamine deficient striatum of the weaver mutant mouse

  Brain Research. 1993;606(2):267-272.
  10

• 240.

  1993

  C. Sola; G. Mengod; W.C. Low; J. Norton; B. Ghetti; J.M. Palacios; L.C. Triarhou

  Regional distribution of amyloid β-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

  European Journal of Neuroscience. 1993;5(11):1442-1454.
  5

• 241.

  1993

  O. Bugiani; G. Giaccone; L. Verga; B. Pollo; B. Frangione; M.R. Farlow; F. Tagliavini; B. Ghetti

  βPP Participates in PrP-amyloid plaques of Gerstmann-Straussler-Scheinker disease, Indiana kindred

  Journal of Neuropathology and Experimental Neurology. 1993;52(1):64-70.
  33

• 242.

  1993

  G. Giaccone; L. Verga; O. Bugiani; B. Frangione; D. Serban; S.B. Prusiner; M.R. Farlow; B. Ghetti; F. Tagliavini

  Erratum: Prion protein preamyloid and amyloid deposits in Gerstmann- Straussler-Scheinker disease, Indiana kindred (Proc. Natl. Acad. Sci. USA (October 1, 1992) 89:19 (9349-9353))

  Proceedings of the National Academy of Sciences of the United States of America. 1993;90(1):362.
  0

• 243.

  1993

  C. Sola; G. Mengod; B. Ghetti; J.M. Palacios; L.C. Triarhou

  Regional distribution of the alternatively spliced isoforms of βAPP RNA transcript in the brain of normal, heterozygous and homozygous weaver mutant mice as revealed by in situ hybridization histochemistry

  Molecular Brain Research. 1993;17(3-4):340-346.
  5

• 244.

  1993

  J.J. Liepnieks; B. Ghetti; M. Farlow; A.D. Roses; M.D. Benson

  Characterization of amyloid fibril β-peptide in familial Alzheimer's disease with APP717 mutations

  Biochemical and Biophysical Research Communications. 1993;197(2):386-392.
  6

• 245.

  1993

  C.M. Vogelweid; T. Verina; J. Norton; R. Harruff; B. Ghetti

  Hypospermatogenesis is the cause of infertility in the male weaver mutant mouse

  J.NEUROGENET. 1993;9(2):89-104.
  16

• 246.

  1993

  J.A. Richter; B. Ghetti; J.R. Simon

  Dopamine-depleting effects of MPTP and reserpine in weaver mutant mice

  Molecular and Chemical Neuropathology. 1993;20(3):219-228.
  0

• 247.

  1993

  A.C. Chang; B. Ghetti

  Embryonic cerebellar graft development during acute phase of gliosis in the cerebellum of pcd mutant mice.

  Chinese Journal of Physiology. 1993;36(3):141-149.
  3

• 248.

  1992

  R.D. Yee; M.R. Farlow; D.A. Suzuki; K.F. Betelak; B. Ghetti

  Abnormal eye movements in Gerstmann-Straussler-Scheinker disease

  Archives of Ophthalmology. 1992;110(1):68-74.
  8

• 249.

  1992

  B. Ghetti; J. Murrell; M.D. Benson; M.R. Farlow

  Spectrum of amyloid β-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):133-139.
  13

• 250.

  1992

  L.C. Triarhou; W.C. Low; B. Ghetti

  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):409-420.
  14

• 251.

  1992

  B. Ghetti; L.C. Triarhou

  Degeneration of mesencephalic dopamine neurons in weaver mutant mice

  Neurochemistry International. 1992;20(SUPPL.):305S-307S.
  14

• 252.

  1992

  L.C. Triarhou; W.C. Low; B. Ghetti

  Serotonin fiber innervation of cerebellar cell suspensions intraparenchymally grafted to the cerebellum of pcd mutant mice

  Neurochemical Research. 1992;17(5):475-482.
  6

• 253.

  1992

  J.A. Richter; E.H. Stotz; B. Ghetti; J.R. Simon

  Comparison of alterations in tyrosine hydroxylase, dopamine levels, and dopamine uptake in the striatum of the weaver mutant mouse

  Neurochemical Research. 1992;17(5):437-441.
  14

• 254.

  1992

  J.R. Simon; B. Ghetti

  Topographic distribution of dopamine uptake, choline uptake, choline acetyltransferase, and GABA uptake in the striata of weaver mutant mice

  Neurochemical Research. 1992;17(5):431-436.
  7

• 255.

  1992

  G. Giaccone; L. Verga; O. Bugiani; B. Frangione; D. Serban; S.B. Prusiner; M.R. Farlow; B. Ghetti; F. Tagliavini

  Prion protein preamyloid and amyloid deposits in Gerstmann-Straussler- Scheinker disease, Indiana kindred

  Proceedings of the National Academy of Sciences of the United States of America. 1992;89(19):9349-9353.
  49

• 256.

  1992

  M. Farlow; B. Ghetti; M.D. Benson; J.S. Farrow; W.E. Van Norstrand; S.L. Wagner

  Low cerebrospinal-fluid concentrations of soluble amyloid β-protein precursor in hereditary Alzheimer's disease

  Lancet. 1992;340(8817):453-454.
  28

• 257.

  1992

  Stephen R. Dlouhy; Karen Hsiao; Martin R. Farlow; Tatiana Foroud; P. Michael Conneally; Patricia Johnson; Stanley B. Prusiner; M.E. Hodes; Bernardino Ghetti

  Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene

  Nature Genetics. 1992;1(1):64-67.
  105

• 258.

  1992

  Karen Hsiao; Stephen R. Dlouhy; Martin R. Farlow; Carin Cass; Maria Da Costa; P. Michael Conneally; M.E. Hodes; Bernardino Ghetti; Stanley B. Prusiner

  Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles

  Nature Genetics. 1992;1(1):68-71.
  102

• 259.

  1992

  L.C. Triarhou; J. Norton; B. Ghetti; J.N. Hingtgen

  Influence of genetic strain background on the magnitude of behavioral recovery observed in weaver mutant mice following bilateral intrastriatal grafting of mesencephalic cell suspensions

  Journal of Neural Transplantation and Plasticity. 1992;3(4):253-254.
  0

• 260.

  1991

  L.C. Triarhou; B. Ghetti

  Stabilisation of neurone number in the inferior olivary complex of aged 'Purkinje cell degeneration' mutant mice

  Acta Neuropathologica. 1991;81(6):597-602.
  20

• 261.

  1991

  O. Bugiani; J. Constantinidis; B. Ghetti; C. Bouras; F. Tagliavini

  Asymmetrical cerebral atrophy in Alzheimer's disease

  Clinical Neuropathology. 1991;10(2):55-60.
  8

• 262.

  1991

  J. Murrell; M. Farlow; B. Ghetti; M.D. Benson

  A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease

  Science. 1991;254(5028):97-99.
  432

• 263.

  1991

  L.C. Triarhou; B. Ghetti

  Serotonin-immunoreactivity in the cerebellum of two neurological mutant mice and the corresponding wild-type genetic stocks

  Journal of Chemical Neuroanatomy. 1991;4(6):421-428.
  13

• 264.

  1991

  B. Ghetti; L.C. Triarhou; C.J. Alyea; S.R. Dlouhy; R.C. Karn

  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.
  4

• 265.

  1991

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

  Amyloid protein of Gerstmann-Straussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58

  EMBO Journal. 1991;10(3):513-519.
  97

• 266.

  1991

  J.R. Simon; H. Yu; J.A. Richter; M.R. Vasko; B. Ghetti

  In vitro release of endogenous dopamine from the striatum of the weaver mutant mouse

  Journal of Neurochemistry. 1991;57(5):1478-1482.
  3

• 267.

  1990

  B. Ghetti; L.C. Triarhou; C.J. Alyea; W.C. Low; A.C. Chang

  Timing of neuronal replacement in cerebellar degenerative ataxia of Purkinje cell type

  Progress in Brain Research. 1990;82:197-202.
  2

• 268.

  1990

  O. Bugiani; G. Giaccone; L. Verga; B. Pollo; B. Ghetti; B. Frangione; F. Tagliavini

  Alzheimer patients and Down patients: Abnormal presynaptic terminals are related to cerebral preamyloid deposits

  Neuroscience Letters. 1990;119(1):56-59.
  17

• 269.

  1990

  G. Giaccone; F. Tagliavini; L. Verga; B. Frangione; M.R. Farlow; O. Bugiani; B. Ghetti

  Neurofibrillary tangles of the Indiana kindred of Gerstmann-Straussler-Scheinker disease share antigenic determinants with those of Alzheimer disease

  Brain Research. 1990;530(2):325-329.
  22

• 270.

  1990

  L.C. Triarhou; P. Brundin; G. Doucet; J. Norton; A. Bjorklund; B. Ghetti

  Intrastriatal implants of mesencephalic cell suspensions in weaver mutant mice: Ultrastructural relationships of dopaminergic dendrites and axons issued from the graft

  Experimental Brain Research. 1990;79(1):3-17.
  7

• 271.

  1990

  L.C. Triarhou; W.C. Low; B. Ghetti

  Dopamine neurone grafting to the weaver mouse neostriatum

  Progress in Brain Research. 1990;82:187-195.
  0

• 272.

  1990

  Y. Kaseda; B. Ghetti; W.C. Low; J. Norton; H. Brittain; L.C. Triarhou; J.A. Richter; J.R. Simon

  Age-related changes in striatal dopamine D2 receptor binding in weaver mice and effects of ventral mesencephalic grafts

  Experimental Brain Research. 1990;83(1):1-8.
  5

• 273.

  1989

  G. Doucet; P. Brundin; S. Seth; Y. Murata; R.E. Strecker; L.C. Triarhou; B. Ghetti; A. Björklund

  Degeneration and graft-induced restoration of dopamine innervation in the weaver mouse neostriatum: a quantitative radioautographic study of [³H]dopamine uptake

  Experimental Brain Research. 1989;77(3):552-568.
  12

• 274.

  1989

  O. Bugiani; G. Giaccone; B. Frangione; B. Ghetti; F. Tagliavini

  Alzheimer patients: preamyloid deposits are more widely distributed than senile plaques throughout the central nervous system

  Neuroscience Letters. 1989;103(3):263-268.
  15

• 275.

  1989

  A.C. Chang; L.C. Triarhou; C.J. Alyea; W.C. Low; B. Ghetti

  Developmental expression of polypeptide PEP-19 in cerebellar cell suspensions transplanted into the cerebellum of pcd mutant mice

  Experimental Brain Research. 1989;76(3):639-645.
  4

• 276.

  1989

  L.C. Triarhou; B. Ghetti

  The dendritic dopamine projection of the substantia nigra: Phenotypic denominator of weaver gene action in hetero- and homozygosity

  Brain Research. 1989;501(2):373-381.
  14

• 277.

  1989

  M.R. Farlow; R.D. Yee; S.R. Dlouhy; P.M. Conneally; B. Azzarelli; B. Ghetti

  Gerstmann-Straussler-Scheinker disease. I. Extending the clinical spectrum

  Neurology. 1989;39(11):1446-1452.
  30

• 278.

  1989

  B. Ghetti; F. Tagliavini; C.L. Masters; K. Beyreuther; G. Giaccone; L. Verga; M.R. Farlow; P.M. Conneally; S.R. Dlouhy; et al.

  Gerstmann-Straussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family

  Neurology. 1989;39(11):1453-1461.
  73

• 279.

  1988

  B. Ghetti; K.W. Perry; R.W. Fuller

  Serotonin concentration and turnover in cerebellum and other brain regions of pcd mutant mice

  Brain Research. 1988;458(2):367-371.
  10

• 280.

  1988

  L.C. Triarhou; W.C. Low; B. Ghetti

  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):11-15.
  1

• 281.

  1988

  L.G. Mendelsohn; M.C. Smith; V.L. Lucaites; G.A. Kerchner; B. Ghetti

  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):361-366.
  4

• 282.

  1988

  L.C. Triarhou; J. Norton; B. Ghetti

  Mesencephalic dopamine cell deficit involves areas A8, A9 and A10 in weaver mutant mice

  Experimental Brain Research. 1988;70(2):256-265.
  83

• 283.

  1988

  L.C. Triarhou; J. Norton; B. Ghetti

  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):221-232.
  9

• 284.

  1988

  W.J. McBride; B. Ghetti

  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):121-125.
  3

• 285.

  1988

  L.C. Triarhou; W.C. Low; J. Norton; B. Ghetti

  Reinstatement of synaptic connectivity in the striatum of weaver mutant mice following transplantation of ventral mesencephalic anlagen

  Journal of Neurocytology. 1988;17(2):233-243.
  2

• 286.

  1988

  G. Giaccone; F. Tagliavini; J.S. Street; B. Ghetti; O. Bugiani

  Progressive supranuclear palsy with hypertrophy of the olives. An immunocytochemical study of the cytoskeleton of argyrophilic neurons

  Acta Neuropathologica. 1988;77(1):14-20.
  10

• 287.

  1987

  M. Gupta; D.L. Felten; B. Ghetti

  Selective loss of monoaminergic neurons in weaver mutant mice - an immunocytochemical study

  Brain Research. 1987;402(2):379-382.
  36

• 288.

  1987

  B. Ghetti; K.W. Perry; R.W. Fuller

  Norepinephrine metabolism in the cerebellum of the Purkinje cell degeneration (pcd) mutant mouse

  Neurochemistry International. 1987;10(1):39-47.
  2

• 289.

  1987

  Yumiko Kaseda; Bernardino Ghetti; Walter C. Low; Judith A. Richter; Jay R. Simon

  Dopamine D₂ receptors increase in the dorsolateral striatum of weaver mutant mice

  Brain Research. 1987;422(1):178-181.
  4

• 290.

  1987

  L.C. Triarhou; W.C. Low; B. Ghetti

  Transplantation of cerebellar anlagen to hosts with genetic cerebellocortical atrophy

  Anatomy and Embryology. 1987;176(2):145-154.
  7

• 291.

  1987

  B. Ghetti; J. Norton; L.C. Triarhou

  Nerve cell atrophy and loss in the inferior olivary complex of 'Purkinje cell degeneration' mutant mice

  Journal of Comparative Neurology. 1987;260(3):409-422.
  32

• 292.

  1987

  L.C. Triarhou; J. Norton; B. Ghetti

  Anterograde transsynaptic degeneration in the deep cerebellar nuclei of Purkinje cell degeneration (pcd) mutant mice

  Experimental Brain Research. 1987;66(3):577-588.
  25

• 293.

  1987

  J.R. Hofstetter; I. Vincent; O. Bugiani; B. Ghetti; J.A. Richter

  Aluminum-induced decreases in choline acetyltransferase, tyrosine hydroxylase, and glutamate decarboxylase in selected regions of rabbit brain

  Neurochemical Pathology. 1987;6(3):177-193.
  15

• 294.

  1987

  L.C. Triarhou; W.C. Low; B. Ghetti

  Synaptic investment of striatal cellular domains by grafted dopamine neurons in weaver mutant mice

  Naturwissenschaften. 1987;74(12):591-593.
  0

• 295.

  1987

  W.C. Low; L.C. Triarhou; Y. Klaseda; J. Norton; B. Ghetti

  Functional innervation of the striatum by ventral mesencephalic grafts in mice with inherited nigrostriatal dopamine deficiency

  Brain Research. 1987;435(1-2):315-321.
  6

• 296.

  1987

  L.C. Triarhou; B. Ghetti

  Neuroanatomical substrate of behavioural impairment in weaver mutant mice

  Experimental Brain Research. 1987;68(2):434-435.
  7

• 297.

  1987

  W.C. Low; L.C. Triarhou; B. Ghetti

  Cerebellar transplants into mutant mice with Purkinje and granule cell degeneration

  Annals of the New York Academy of Sciences. 1987;495:740-744.
  3

• 298.

  1986

  D.L. Felten; S.Y. Felten; K.W. Perry; R.W. Fuller; J.I. Nurnberger; B. Ghetti

  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):783-793.
  11

• 299.

  1986

  L.C. Triarhou; B. Ghetti

  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.
  12

• 300.

  1986

  B. Ghetti; O. Bugiani

  'Aluminium disease' and Alzheimer's disease

  Neurobiology of Aging. 1986;7(6):536-537.
  0

• 301.

  1986

  L.C. Triarhou; W.C. Low; B. Ghetti

  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):8789-8793.
  17

• 302.

  1985

  Y. Sato; S.U. Kim; B. Ghetti

  Induction of neurofibrillary tangles in cultured mouse neurons by maytanprine

  Journal of the Neurological Sciences. 1985;68(2-3):191-203.
  2

• 303.

  1985

  B. Azzarelli; J. Muller; B. Ghetti

  Cerebral plaques in familial Alzheimer's disease (Gerstmann-Straussler-Scheinker variant?)

  Acta Neuropathologica. 1985;65(3-4):235-246.
  15

• 304.

  1985

  B. Ghetti; M. Musicco; J. Norton; O. Bugiani

  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.
  7

• 305.

  1985

  O. Bugiani; D. Brancaccio; B. Ghetti

  Progressive dialytic encephalopathy and the problem of aluminum neurotoxicity

  Clinical Nephrology. 1985;24(SUPPL. 1):S20-S25.
  0

• 306.

  1985

  L.C. Triarhou; J. Norton; O. Bugiani; B. Ghetti

  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):407-430.
  2

• 307.

  1985

  F.M. Vaccarino; B. Ghetti; J.I. Nurnberger Sr.

  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):70-78.
  5

• 308.

  1983

  B. Ghetti; P. Gambetti

  Comparative immunocytochemical characterization of neurofibrillary tangles in experimental maytansine and aluminum encephalopathies

  Brain Research. 1983;276(2):388-393.
  5

• 309.

  1983

  F.M. Vaccarino; B. Ghetti; S.E. Wade; M.A. Rea; M.H. Aprison

  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):311-323.
  1

• 310.

  1983

  P. Gambetti; G. Shecket; B. Ghetti; A. Hirano; D. Dahl

  Neurofibrillary changes in human brain. An immunocytochemical study with a neurofilament antiserum

  Journal of Neuropathology and Experimental Neurology. 1983;42(1):69-79.
  9

• 311.

  1982

  M.J. Schmidt; B.D. Sawyer; K.W. Perry; R.W. Fuller; M.M. Foreman; B. Ghetti

  Dopamine deficiency in the weaver mutant mouse

  Journal of Neuroscience. 1982;2(3):376-380.
  95

• 312.

  1982

  J.P. Schwartz; B. Ghetti; L. Truex; M.J. Schmidt

  Increase of a nerve growth factor-like protein in the cerebellum of pcd mutant mice

  Journal of Neuroscience Research. 1982;8(2-3):205-211.
  1

• 313.

  1982

  O. Bugiani; B. Ghetti

  Progressing encephalomyelopathy with muscular atrophy, induced by aluminum powder

  Neurobiology of Aging. 1982;3(3):209-222.
  16

• 314.

  1981

  A. Routtenberg; D.G. Morgan; R.G. Conway; M.J. Schmidt; B. Ghetti

  Human brain protein phosphorylation in vitro: Cyclic AMP stimulation of electrophoretically-separated substrates

  Brain Research. 1981;222(2):323-333.
  1

• 315.

  1981

  Bernardino Ghetti; Ray W. Fuller; Barry D. Sawyer; Susan K. Hemrick-Luecke; Michael J. Schmidt

  Purkinje cell loss and the noradrenergic system in the cerebellum of pcd mutant mice

  Brain Research Bulletin. 1981;7(6):711-714.
  9

• 316.

  1981

  B. Ghetti; L. Truex; B. Sawyer; S. Strada; M. Schmidt

  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):789-801.
  4

• 317.

  1980

  M.J. Schmidt; L.L. Truex; B. Ghetti; A. Routtenberg

  Cyclic AMP-dependent protein kinase activity in human brain across age

  Journal of Neurochemistry. 1980;35(1):261-265.
  1

• 318.

  1980

  M.J. Schmidt; B. Ghetti

  Exaggerated norepinephrine-stimulated accumulation of cyclic AMP in vitro in cerebellar slices from pcd mutant mice following Purkinje cell loss

  Journal of Neural Transmission - General Section. 1980;48(1):49-56.
  2

• 319.

  1980

  S.U. Kim; M. Tomonaga; B. Ghetti

  Neurofibrillary degeneration in cultured adult mouse neurons induced by maytansine

  Acta Neuropathologica. 1980;52(2):161-164.
  1

• 320.

  1979

  A. Maggi; M.J. Schmidt; B. Ghetti; S.J. Enna

  Effect of aging on neurotransmitter receptor binding in rat and human brain

  Life Sciences. 1979;24(4):367-373.
  8

• 321.

  1979

  B. Ghetti

  Induction of neurofibrillary degeneration following treatment with maytansine in vivo

  Brain Research. 1979;163(1):9-19.
  3

• 322.

  1975

  B. Ghetti; D.S. Horoupian; H.M. Wisniewski

  Acute and long-term transneuronal response of dendrites of lateral geniculate neurons following transection of the primary visual afferent pathway.

  Advances in neurology. 1975;12:401-424.
  5

• 323.

  1974

  K. Kristensson; B. Ghetti; H.M. Wisniewski

  Study on the propagation of Herpes simplex virus (type 2) into the brain after intraocular injection

  Brain Research. 1974;69(2):189-201.
  29

• 324.

  1974

  R.D. Cook; B. Ghetti; H.M. Wisniewski

  The pattern of Wallerian degeneration in the optic nerve of newborn kittens: an ultrastructural study

  Brain Research. 1974;75(2):261-275.
  7

• 325.

  1974

  J.K. Korthals; H.M. Wisniewski; B. Ghetti; R.D. Cook

  The fate of the axon and its terminal in the Pacinian corpuscle following sciatic nerve section

  Journal of Neurocytology. 1974;3(3):385-403.
  1

• 326.

  1973

  G.C. Guazzi; B. Ghetti; F. Barbieri; A. Cecio

  Myoclonus epilepsy with cherry red spot in adult: A peculiar form of mucopolysaccharidosis. (A clinical, genetical, chemical and ultrastructural study)

  Acta Neurologica. 1973;28(5):542-549.
  4

• 327.

  1973

  H.M. Wisniewski; B. Ghetti; R.D. Terry

  Neuritic (senile) plaques and filamentous changes in aged rhesus monkeys

  Journal of Neuropathology and Experimental Neurology. 1973;32(4):566-584.
  69

• 328.

  1973

  Dikran S. Horoupian; Bernardino Ghetti; Henryk M. Wisniewski

  Retrograde transneuronal degeneration of optic fibers and their terminals in lateral geniculate nucleus of Rhesus monkey

  Brain Research. 1973;49(2):257-275.
  1

• 329.

  1972

  Henryk M. Wisniewski; Bernardino Ghetti; Dikran S. Horoupian

  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.
  1

• 330.

  1972

  Bernardino Ghetti; Dikran S. Horoupian; Henryk M. Wisniewski

  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.
  4

• 331.

  1972

  Bernardino Ghetti; Henryk M. Wisniewski

  On degeneration of terminals in the cat striate cortex

  Brain Research. 1972;44(2):630-635.
  2

• 332.

  1971

  B. Ghetti; A. Amati; M.V. Turra; A. Pacini; M. Del Vecchio; G.C. Guazzi

  Werdnig-Hoffmann-Wohlfart-Kugelberg-Welander disease. Nosological unity and clinical variability in intrafamilial cases.

  Acta Geneticae Medicae et Gemellologiae. 1971;20(1):43-58.
  2

• 333.

  1971

  M. Del Vecchio; A. Cerillo; B. Ghetti; A. Amati; C. Signorelli; G. Cedrola; G.C. Guazzi

  Genetic study of 2 families (23 subjects) with von Recklinghausen's disease with dominant autosomal heredity

  Acta Neurologica. 1971;26(3):319-360.
  0

• 334.

  1971

  F. Bravaccio; M. Del Vecchio; C. Paolozzi; B. Ghetti; B. Tripaldelli; A. Amati; G.C. Guazzi

  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):361-374.
  0

• 335.

  1971

  Cedric S. Raine; Bernardino Ghetti; Michael L. Shelanski

  On the association between microtubules and mitochondria within axons

  Brain Research. 1971;34(2):389-393.
  5

• 336.

  1970

  B. Ghetti; G.C. Guazzi; R.V. De Masi; A. Cecio

  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):252-260.
  1

• 337.

  1970

  G.C. Guazzi; V. Ventruto; M. Del Vecchio; G.R. Fazzi; B. Ghetti; G. Salvati; P. Vertucci; A. Bianchi

  Genetic and immunologic study of 2 families affected by ataxia-telangiectastia of Mme Louis-Bar

  Acta Neurologica. 1970;25(5):551-577.
  0

• 338.

  1970

  G.C. Guazzi; B. Ghetti; M. Del Vecchio; S. Striano

  Genetic study of a family with juvenile myoclonus-epilepsy with cherry red spots in the fundus oculi

  Bollettino della Societa italiana di biologia sperimentale. 1970;46(9):452-455.
  0

• 339.

  1970

  B. Ghetti; A. Cecio; R.V. De Masi; G.C. Guazzi

  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 Societa italiana di biologia sperimentale. 1970;46(9):455-457.
  0

• 340.

  1970

  A. Cecio; B. Ghetti; R.V. De Masi; G.C. Guazzi

  Ultrastructure of hepatic biopsy in a 29-year-old patient with epilepsy-myoclonus with cherry red spots in the fundus oculi

  Bollettino della Societa italiana di biologia sperimentale. 1970;46(9):457-459.
  0

• 341.

  1970

  C. Fiore; B. Ghetti; A. Bertolino; R. Fazzi; G.C. Guazzi

  Louis-Bar ataxia telangiectasia: study of the first Italian case

  Rassegna Internazionale di Clinica e Terapia. 1970;50(10):599-601.
  0

• 342.

  1969

  G.B. Cassano; P.L. Viola; B. Ghetti; L. Amaducci

  The distribution of inhaled mercury(Hg203) vapors in the brain of rats and mice.

  Journal of Neuropathology and Experimental Neurology. 1969;28(2):308-320.
  10

• 343.

  1969

  A. Bertolino; C. Fiore; L. Morcaldi; L. Pinto; B. Ghetti; G.C. Guazzi

  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):1331-1347.
  0

• 344.

  1967

  G.B. Cassano; G.F. Placidi; B. Ghetti

  Comparative study of the fetal distribution of some psychotropic and hypnotic drugs

  Rivista di Neurobiologia. 1967;13(1):105-114.
  0

• 345.

  1967

  G.B. Cassano; B. Ghetti; E. Gljozzi; E. Hansson

  Autoradiographic distribution study of "short acting" and "long acting" barbiturates: S-thiopentone and ¹⁴C-phenobarbitone

  British Journal of Anaesthesia. 1967;39(1):11-20.
  3