Orso Bugiani - Publications

Affiliations: 
University of Milan, Milano, Lombardia, Italy 
Area:
Neuropathology

105 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Bugiani O. The puzzle of preserved cognition in the oldest old. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. PMID 31713754 DOI: 10.1007/S10072-019-04111-Y  0.36
2019 Forloni G, Chiesa R, Bugiani O, Salmona M, Tagliavini F. PrP 106-126 - 25 years after. Neuropathology and Applied Neurobiology. PMID 30635947 DOI: 10.1111/Nan.12538  0.429
2018 Saracino D, Allegorico L, Barbarulo AM, Pollo B, Giaccone G, D'Amico A, D'Incerti L, Bugiani O, Di Iorio G, Sampaolo S, Melone MAB. Neuro-Behçet's disease presenting as an isolated progressive cognitive and behavioral syndrome. Neurocase. 1-4. PMID 30583716 DOI: 10.1080/13554794.2018.1561898  0.321
2015 Alafuzoff I, Pikkarainen M, Neumann M, Arzberger T, Al-Sarraj S, Bodi I, Bogdanovic N, Bugiani O, Ferrer I, Gelpi E, Gentleman S, Giaccone G, Graeber MB, Hortobagyi T, Ince PG, et al. Erratum to: Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium. Journal of Neural Transmission (Vienna, Austria : 1996). 122: 973-4. PMID 25418279 DOI: 10.1007/S00702-014-1337-5  0.305
2014 Puoti G, Lerza MC, Ferretti MG, Bugiani O, Tagliavini F, Rossi G. A mutation in the 5'-UTR of GRN gene associated with frontotemporal lobar degeneration: phenotypic variability and possible pathogenetic mechanisms. Journal of Alzheimer's Disease : Jad. 42: 939-47. PMID 25024321 DOI: 10.3233/Jad-140717  0.324
2013 Moro ML, Giaccone G, Lombardi R, Indaco A, Uggetti A, Morbin M, Saccucci S, Di Fede G, Catania M, Walsh DM, Demarchi A, Rozemuller A, Bogdanovic N, Bugiani O, Ghetti B, et al. Erratum to: APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38 Acta Neuropathologica. 125: 467-467. DOI: 10.1007/S00401-013-1094-9  0.366
2012 Moro ML, Giaccone G, Lombardi R, Indaco A, Uggetti A, Morbin M, Saccucci S, Di Fede G, Catania M, Walsh DM, Demarchi A, Rozemuller A, Bogdanovic N, Bugiani O, Ghetti B, et al. APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38. Acta Neuropathologica. 124: 809-21. PMID 23143229 DOI: 10.1007/S00401-012-1061-X  0.423
2011 Bugiani O. Alzheimer's disease: ageing-related or age-related? New hypotheses from an old debate. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 32: 1241-7. PMID 21567180 DOI: 10.1007/S10072-011-0614-4  0.35
2011 Gallo M, Marcello N, Curcio SA, Colao R, Geracitano S, Bernardi L, Anfossi M, Puccio G, Frangipane F, Clodomiro A, Mirabelli M, Vasso F, Smirne N, Muraca G, Di Lorenzo R, ... ... Bugiani O, et al. A novel pathogenic PSEN1 mutation in a family with Alzheimer's disease: phenotypical and neuropathological features. Journal of Alzheimer's Disease : Jad. 25: 425-31. PMID 21422519 DOI: 10.3233/Jad-2011-110185  0.424
2011 Bellucci A, Bugiani O, Ghetti B, Spillantini MG. Presence of reactive microglia and neuroinflammatory mediators in a case of frontotemporal dementia with P301S mutation. Neuro-Degenerative Diseases. 8: 221-9. PMID 21212632 DOI: 10.1159/000322228  0.365
2010 Binelli S, Agazzi P, Canafoglia L, Scaioli V, Panzica F, Visani E, Di Fede G, Giaccone G, Bizzi A, Bugiani O, Avanzini G, Tagliavini F, Franceschetti S. Myoclonus in Creutzfeldt-Jakob disease: polygraphic and video-electroencephalography assessment of 109 patients. Movement Disorders : Official Journal of the Movement Disorder Society. 25: 2818-27. PMID 20939057 DOI: 10.1002/Mds.23397  0.325
2010 Bugiani O, Giaccone G, Rossi G, Mangieri M, Capobianco R, Morbin M, Mazzoleni G, Cupidi C, Marcon G, Giovagnoli A, Bizzi A, Di Fede G, Puoti G, Carella F, Salmaggi A, et al. Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP. Archives of Neurology. 67: 987-95. PMID 20697050 DOI: 10.1001/Archneurol.2010.178  0.397
2010 Cupidi C, Capobianco R, Goffredo D, Marcon G, Ghetti B, Bugiani O, Tagliavini F, Giaccone G. Neocortical variation of Abeta load in fully expressed, pure Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 19: 57-68. PMID 20061626 DOI: 10.3233/Jad-2010-1205  0.43
2009 Giaccone G, Di Fede G, Mangieri M, Limido L, Capobianco R, Suardi S, Grisoli M, Binelli S, Fociani P, Bugiani O, Tagliavini F. A novel phenotype of sporadic Creutzfeldt-Jakob disease. Bmj Case Reports. 2009. PMID 21686549 DOI: 10.1136/Bcr.09.2008.0945  0.435
2009 Alafuzoff I, Thal DR, Arzberger T, Bogdanovic N, Al-Sarraj S, Bodi I, Boluda S, Bugiani O, Duyckaerts C, Gelpi E, Gentleman S, Giaccone G, Graeber M, Hortobagyi T, Höftberger R, et al. Assessment of beta-amyloid deposits in human brain: a study of the BrainNet Europe Consortium. Acta Neuropathologica. 117: 309-20. PMID 19184666 DOI: 10.1007/S00401-009-0485-4  0.325
2008 Alafuzoff I, Arzberger T, Al-Sarraj S, Bodi I, Bogdanovic N, Braak H, Bugiani O, Del-Tredici K, Ferrer I, Gelpi E, Giaccone G, Graeber MB, Ince P, Kamphorst W, King A, et al. Staging of neurofibrillary pathology in Alzheimer's disease: a study of the BrainNet Europe Consortium. Brain Pathology (Zurich, Switzerland). 18: 484-96. PMID 18371174 DOI: 10.1111/J.1750-3639.2008.00147.X  0.379
2008 Giaccone G, Mangieri M, Capobianco R, Limido L, Hauw JJ, Haïk S, Fociani P, Bugiani O, Tagliavini F. Tauopathy in human and experimental variant Creutzfeldt-Jakob disease. Neurobiology of Aging. 29: 1864-73. PMID 17560687 DOI: 10.1016/J.Neurobiolaging.2007.04.026  0.484
2007 Giaccone G, Di Fede G, Mangieri M, Limido L, Capobianco R, Suardi S, Grisoli M, Binelli S, Fociani P, Bugiani O, Tagliavini F. A novel phenotype of sporadic Creutzfeldt-Jakob disease. Journal of Neurology, Neurosurgery, and Psychiatry. 78: 1379-82. PMID 18024694 DOI: 10.1136/Jnnp.2007.115444  0.435
2007 Baba Y, Baker MC, Le Ber I, Brice A, Maeck L, Kohlhase J, Yasuda M, Stoppe G, Bugiani O, Sperfeld AD, Tsuboi Y, Uitti RJ, Farrer MJ, Ghetti B, Hutton ML, 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 (Vienna, Austria : 1996). 114: 947-50. PMID 17318302 DOI: 10.1007/S00702-007-0632-9  0.353
2007 Tagliavini F, Mangieri M, Capobianco R, Hauw J, Haik S, Limido L, Fociani P, Bugiani O, Giaccone G. Tauopathy in human and experimental variant Creutzfeldt-Jakob disease: 48.6 Journal of Neuropathology and Experimental Neurology. 66: 430. DOI: 10.1097/01.Jnen.0000268852.28994.6A  0.328
2006 Alafuzoff I, Pikkarainen M, Al-Sarraj S, Arzberger T, Bell J, Bodi I, Bogdanovic N, Budka H, Bugiani O, Ferrer I, Gelpi E, Giaccone G, Graeber MB, Hauw JJ, Kamphorst W, et al. Interlaboratory comparison of assessments of Alzheimer disease-related lesions: a study of the BrainNet Europe Consortium. Journal of Neuropathology and Experimental Neurology. 65: 740-57. PMID 16896308 DOI: 10.1097/01.Jnen.0000229986.17548.27  0.387
2006 Binelli S, Agazzi P, Giaccone G, Will RG, Bugiani O, Franceschetti S, Tagliavini F. Periodic electroencephalogram complexes in a patient with variant Creutzfeldt-Jakob disease. Annals of Neurology. 59: 423-7. PMID 16437565 DOI: 10.1002/Ana.20768  0.333
2006 Cupidi C, Giaccone G, Capobianco R, Ghetti B, Bugiani O, Tagliavini F. P3-200: Relationship between neurofibrillary pathology and Aβ deposition in Alzheimer disease Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.1468  0.418
2006 Bugiani O. S2-02-01: Aβ-related cerebral amyloid angiopathy Alzheimer's & Dementia. 2: S24-S25. DOI: 10.1016/J.Jalz.2006.05.081  0.363
2005 Puoti G, Giaccone G, Mangieri M, Limido L, Fociani P, Zerbi P, Suardi S, Rossi G, Iussich S, Capobianco R, Di Fede G, Marcon G, Cotrufo R, Filippini G, Bugiani O, et al. Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPSc. Journal of Neuropathology and Experimental Neurology. 64: 902-9. PMID 16215462 DOI: 10.1097/01.Jnen.0000183346.19447.55  0.394
2005 Baba Y, Tsuboi Y, Baker MC, Uitti RJ, Hutton ML, Dickson DW, Farrer M, Putzke JD, Woodruff BK, Ghetti B, Murrell JR, Boeve BF, Petersen RC, Verpillat P, Brice A, ... ... Bugiani O, et al. The effect of tau genotype on clinical features in FTDP-17. Parkinsonism & Related Disorders. 11: 205-8. PMID 15878580 DOI: 10.1016/J.Parkreldis.2005.01.003  0.31
2004 Marcon G, Giaccone G, Cupidi C, Balestrieri M, Beltrami CA, Finato N, Bergonzi P, Sorbi S, Bugiani O, Tagliavini F. Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 gene. Journal of Neuropathology and Experimental Neurology. 63: 199-209. PMID 15055444 DOI: 10.1093/Jnen/63.3.199  0.464
2003 Pietrini V, Puoti G, Limido L, Rossi G, Di Fede G, Giaccone G, Mangieri M, Tedeschi F, Bondavalli A, Mancia D, Bugiani O, Tagliavini F. Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene. Neurology. 61: 1288-91. PMID 14610142  0.301
2003 Soliveri P, Rossi G, Monza D, Tagliavini F, Piacentini S, Albanese A, Bugiani O, Girotti F. A case of dementia parkinsonism resembling progressive supranuclear palsy due to mutation in the tau protein gene. Archives of Neurology. 60: 1454-6. PMID 14568818 DOI: 10.1001/Archneur.60.10.1454  0.358
2003 Salmona M, Morbin M, Massignan T, Colombo L, Mazzoleni G, Capobianco R, Diomede L, Thaler F, Mollica L, Musco G, Kourie JJ, Bugiani O, Sharma D, Inouye H, Kirschner DA, et al. Structural properties of Gerstmann-Straussler-Scheinker disease amyloid protein. The Journal of Biological Chemistry. 278: 48146-53. PMID 12970341 DOI: 10.1074/Jbc.M307295200  0.443
2003 Rossi G, Salmona M, Forloni G, Bugiani O, Tagliavini F. Therapeutic approaches to prion diseases. Clinics in Laboratory Medicine. 23: 187-208. PMID 12733432 DOI: 10.1016/S0197-4580(00)83270-4  0.384
2003 Ghetti B, Tagliavini F, Takao M, Bugiani O, Piccardo P. Hereditary prion protein amyloidoses. Clinics in Laboratory Medicine. 23: 65-85, viii. PMID 12733425 DOI: 10.1016/S0272-2712(02)00064-1  0.46
2002 Forloni G, Iussich S, Awan T, Colombo L, Angeretti N, Girola L, Bertani I, Poli G, Caramelli M, Grazia Bruzzone M, Farina L, Limido L, Rossi G, Giaccone G, Ironside JW, ... Bugiani O, et al. Tetracyclines affect prion infectivity. Proceedings of the National Academy of Sciences of the United States of America. 99: 10849-54. PMID 12149459 DOI: 10.1073/Pnas.162195499  0.38
2001 Takao M, Ghetti B, Murrell JR, Unverzagt FW, Giaccone G, Tagliavini F, Bugiani O, Piccardo P, Hulette CM, Crain BJ, Farlow MR, Heyman A. Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizures. Journal of Neuropathology and Experimental Neurology. 60: 1137-52. PMID 11764087 DOI: 10.1093/Jnen/60.12.1137  0.397
2001 Tagliavini F, Forloni G, D'Ursi P, Bugiani O, Salmona M. Studies on peptide fragments of prion proteins. Advances in Protein Chemistry. 57: 171-201. PMID 11447690 DOI: 10.1016/S0065-3233(01)57022-9  0.367
2001 Piccardo P, Liepnieks JJ, William A, Dlouhy SR, Farlow MR, Young K, Nochlin D, Bird TD, Nixon RR, Ball MJ, DeCarli C, Bugiani O, Tagliavini F, Benson MD, Ghetti B. Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations. The American Journal of Pathology. 158: 2201-7. PMID 11395398 DOI: 10.1016/S0002-9440(10)64692-5  0.358
2001 Tagliavini F, Lievens PM, Tranchant C, Warter JM, Mohr M, Giaccone G, Perini F, Rossi G, Salmona M, Piccardo P, Ghetti B, Beavis RC, Bugiani O, Frangione B, Prelli F. A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V. The Journal of Biological Chemistry. 276: 6009-15. PMID 11087738 DOI: 10.1074/Jbc.M007062200  0.427
2000 Sorbi S, Alberoni M, Alfieri P, Amici S, Antana D, Appollonio I, Avanzi S, Bartoli A, Bergamasco B, Bracco L, Bruni A, Bugiani O, Caffarra P, Caltagirone C, Carolei A, et al. Guidelines for the diagnosis of dementia and Alzheimer's disease Neurological Sciences. 21: 187-194. PMID 11214656 DOI: 10.1007/S100720070075  0.306
2000 Nardocci N, Morbin M, Bugiani M, Lamantea E, Bugiani O. Neuronal ceroid lipofuscinosis: detection of atypical forms. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 21: S57-61. PMID 11073229 DOI: 10.1007/S100720070041  0.392
2000 Thellung S, Florio T, Villa V, Corsaro A, Arena S, Amico C, Robello M, Salmona M, Forloni G, Bugiani O, Tagliavini F, Schettini G. Apoptotic cell death and impairment of L-type voltage-sensitive calcium channel activity in rat cerebellar granule cells treated with the prion protein fragment 106-126. Neurobiology of Disease. 7: 299-309. PMID 10964602 DOI: 10.1006/Nbdi.2000.0301  0.313
2000 Puoti G, Rossi G, Giaccone G, Awan T, Lievens PM, Defanti CA, Tagliavini F, Bugiani O. Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutation. Annals of Neurology. 48: 269-70. PMID 10939584 DOI: 10.1002/1531-8249(200008)48:2<269::Aid-Ana24>3.0.Co;2-V  0.337
2000 Rossi G, Giaccone G, Giampaolo L, Iussich S, Puoti G, Frigo M, Cavaletti G, Frattola L, Bugiani O, Tagliavini F. Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene. Neurology. 55: 405-10. PMID 10932276  0.316
2000 Tagliavini F, Forloni G, Colombo L, Rossi G, Girola L, Canciani B, Angeretti N, Giampaolo L, Peressini E, Awan T, De Gioia L, Ragg E, Bugiani O, Salmona M. Tetracycline affects abnormal properties of synthetic PrP peptides and PrP(Sc) in vitro. Journal of Molecular Biology. 300: 1309-22. PMID 10903871 DOI: 10.1006/Jmbi.2000.3840  0.425
2000 Bugiani O. FTDP-17: phenotypical heterogeneity within P301S. Annals of Neurology. 48: 126. PMID 10894228 DOI: 10.1002/1531-8249(200007)48:1<126::Aid-Ana21>3.0.Co;2-N  0.387
2000 Bugiani O, Giaccone G, Piccardo P, Morbin M, Tagliavini F, Ghetti B. Neuropathology of Gerstmann-Sträussler-Scheinker disease. Microscopy Research and Technique. 50: 10-5. PMID 10871543 DOI: 10.1002/1097-0029(20000701)50:1<10::Aid-Jemt3>3.0.Co;2-6  0.469
2000 Miravalle L, Tokuda T, Chiarle R, Giaccone G, Bugiani O, Tagliavini F, Frangione B, Ghiso J. Substitutions at codon 22 of Alzheimer's abeta peptide induce diverse conformational changes and apoptotic effects in human cerebral endothelial cells. The Journal of Biological Chemistry. 275: 27110-6. PMID 10821838 DOI: 10.1074/Jbc.M003154200  0.437
2000 Thellung S, Florio T, Corsaro A, Arena S, Merlino M, Salmona M, Tagliavini F, Bugiani O, Forloni G, Schettini G. Intracellular mechanisms mediating the neuronal death and astrogliosis induced by the prion protein fragment 106-126. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 18: 481-92. PMID 10817932 DOI: 10.1016/S0736-5748(00)00005-8  0.409
2000 Giaccone G, Iussich S, Puoti G, Rossi G, Goffredo D, Tagliavini F, Bugiani O. Topographic distribution of PRPRES in Creutzfeldt-Jakob disease as revealed by immunohistochemistry Neurobiology of Aging. 21: 54. DOI: 10.1016/S0197-4580(00)82919-X  0.331
2000 Puoti G, Giaccone G, Rossi G, Canciani B, Bugiani O, Tagliavini F. Sporadic creutzfeldt-Jakob disease coexistence of biochemically distinct types of PRPSC in the same brain Neurobiology of Aging. 21: 149. DOI: 10.1016/S0197-4580(00)82473-2  0.353
1999 Bugiani O, Murrell JR, Giaccone G, Hasegawa M, Ghigo G, Tabaton M, Morbin M, Primavera A, Carella F, Solaro C, Grisoli M, Savoiardo M, Spillantini MG, Tagliavini F, Goedert M, et al. Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau. Journal of Neuropathology and Experimental Neurology. 58: 667-77. PMID 10374757 DOI: 10.1097/00005072-199906000-00011  0.36
1999 Marcon G, Giaccone G, Canciani B, Cajola L, Rossi G, De Gioia L, Salmona M, Bugiani O, Tagliavini F. A betaPP peptide carboxyl-terminal to Abeta is neurotoxic. The American Journal of Pathology. 154: 1001-7. PMID 10233838 DOI: 10.1016/S0002-9440(10)65352-7  0.398
1999 Silei V, Fabrizi C, Venturini G, Salmona M, Bugiani O, Tagliavini F, Lauro GM. Activation of microglial cells by PrP and beta-amyloid fragments raises intracellular calcium through L-type voltage sensitive calcium channels. Brain Research. 818: 168-70. PMID 9914452 DOI: 10.1016/S0006-8993(98)01272-4  0.359
1998 Florio T, Thellung S, Amico C, Robello M, Salmona M, Bugiani O, Tagliavini F, Forloni G, Schettini G. Prion protein fragment 106-126 induces apoptotic cell death and impairment of L-type voltage-sensitive calcium channel activity in the GH3 cell line. Journal of Neuroscience Research. 54: 341-52. PMID 9819139 DOI: 10.1002/(Sici)1097-4547(19981101)54:3<341::Aid-Jnr5>3.0.Co;2-G  0.3
1998 Piccardo P, Dlouhy SR, Lievens PM, Young K, Bird TD, Nochlin D, Dickson DW, Vinters HV, Zimmerman TR, Mackenzie IR, Kish SJ, Ang LC, De Carli C, Pocchiari M, Brown P, ... ... Bugiani O, et al. Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity. Journal of Neuropathology and Experimental Neurology. 57: 979-88. PMID 9786248 DOI: 10.1097/00005072-199810000-00010  0.424
1997 Tagliavini F, McArthur RA, Canciani B, Giaccone G, Porro M, Bugiani M, Lievens PM, Bugiani O, Peri E, Dall'Ara P, Rocchi M, Poli G, Forloni G, Bandiera T, Varasi M, et al. Effectiveness of anthracycline against experimental prion disease in Syrian hamsters. Science (New York, N.Y.). 276: 1119-22. PMID 9148807 DOI: 10.1126/science.276.5315.1119  0.34
1996 Diomede L, Sozzani S, Luini W, Algeri M, De Gioia L, Chiesa R, Lievens PM, Bugiani O, Forloni G, Tagliavini F, Salmona M. Activation effects of a prion protein fragment [PrP-(106-126)] on human leucocytes. The Biochemical Journal. 320: 563-70. PMID 8973567 DOI: 10.1042/Bj3200563  0.351
1996 Chiesa R, Angeretti N, Lucca E, Salmona M, Tagliavini F, Bugiani O, Forloni G. Clusterin (SGP-2) induction in rat astroglial cells exposed to prion protein fragment 106-126. The European Journal of Neuroscience. 8: 589-97. PMID 8963451 DOI: 10.1111/J.1460-9568.1996.Tb01244.X  0.321
1996 Piccardo P, Seiler C, Dlouhy SR, Young K, Farlow MR, Prelli F, Frangione B, Bugiani O, Tagliavini F, Ghetti B. Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred). Journal of Neuropathology and Experimental Neurology. 55: 1157-63. PMID 8939199 DOI: 10.1097/00005072-199611000-00007  0.437
1996 Forloni G, Tagliavini F, Bugiani O, Salmona M. Amyloid in Alzheimer's disease and prion-related encephalopathies: studies with synthetic peptides. Progress in Neurobiology. 49: 287-315. PMID 8888112 DOI: 10.1016/0301-0082(96)00013-5  0.403
1996 Forloni G, Bugiani O, Tagliavini F, Salmona M. Apoptosis-mediated neurotoxicity induced by beta-amyloid and PrP fragments. Molecular and Chemical Neuropathology / Sponsored by the International Society For Neurochemistry and the World Federation of Neurology and Research Groups On Neurochemistry and Cerebrospinal Fluid. 28: 163-71. PMID 8871955 DOI: 10.1007/Bf02815218  0.376
1996 Ghetti B, Piccardo P, Frangione B, Bugiani O, Giaccone G, Young K, Prelli F, Farlow MR, Dlouhy SR, Tagliavini F. Prion protein amyloidosis. Brain Pathology (Zurich, Switzerland). 6: 127-45. PMID 8737929 DOI: 10.1111/J.1750-3639.1996.Tb00796.X  0.478
1996 Ghetti B, Piccardo P, Spillantini MG, Ichimiya Y, Porro M, Perini F, Kitamoto T, Tateishi J, Seiler C, Frangione B, Bugiani O, Giaccone G, Prelli F, Goedert M, Dlouhy SR, et al. Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP. Proceedings of the National Academy of Sciences of the United States of America. 93: 744-8. PMID 8570627 DOI: 10.1073/Pnas.93.2.744  0.458
1996 Young K, Piccardo P, Tagliavini F, Giaccone G, Bugiani O, Dlouhy SR, Clark HB, Ghetti B. 165 Prior protein (PrP) residue 129 Val in Gerstmann-Sträussler-Scheinker (GSS) disease with mutation PRNP P102L Neurobiology of Aging. 17. DOI: 10.1016/S0197-4580(96)80167-9  0.39
1996 Tagliavini F, Prelli F, Salmona M, Giaccone G, Ghetti B, Bugiani O, Frangione B, Forloni G. 161 PrP peptides and pathogenesis of prion diseases Neurobiology of Aging. 17. DOI: 10.1016/S0197-4580(96)80163-1  0.37
1996 Ghetti B, Piccardo P, Frangione B, Bugiani O, Giaccone G, Young K, Prelli F, Farlow MR, Dlouhy SR, Tagliavini F. Prion protein hereditary amyloidosis: Parenchymal and vascular Seminars in Virology. 7: 189-200. DOI: 10.1006/Smvy.1996.0024  0.461
1995 Budka H, Aguzzi A, Brown P, Brucher JM, Bugiani O, Gullotta F, Haltia M, Hauw JJ, Ironside JW, Jellinger K. Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathology (Zurich, Switzerland). 5: 459-66. PMID 8974629 DOI: 10.1111/J.1750-3639.1995.Tb00625.X  0.427
1995 Budka H, Aguzzi A, Brown P, Brucher JM, Bugiani O, Collinge J, Diringer H, Gullotta F, Haltia M, Hauw JJ. Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases) Brain Pathology (Zurich, Switzerland). 5: 319-22. PMID 8520732 DOI: 10.1111/J.1750-3639.1995.Tb00609.X  0.316
1995 Ghetti B, Dlouhy SR, Giaccone G, Bugiani O, Frangione B, Farlow MR, Tagliavini F. Gerstmann-Sträussler-Scheinker disease and the Indiana kindred. Brain Pathology (Zurich, Switzerland). 5: 61-75. PMID 7767492 DOI: 10.1111/J.1750-3639.1995.Tb00578.X  0.429
1995 Piccardo P, Ghetti B, Dickson DW, Vinters HV, Giaccone G, Bugiani O, Tagliavini F, Young K, Dlouhy SR, Seiler C. Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165. Journal of Neuropathology and Experimental Neurology. 54: 790-801. PMID 7595652 DOI: 10.1097/00005072-199511000-00006  0.457
1995 Smith MA, Siedlak SL, Richey PL, Mulvihill P, Ghiso J, Frangione B, Tagliavini F, Giaccone G, Bugiani O, Praprotnik D. Tau protein directly interacts with the amyloid beta-protein precursor: implications for Alzheimer's disease. Nature Medicine. 1: 365-9. PMID 7585068 DOI: 10.1038/Nm0495-365  0.409
1995 Tagliavini F, Prelli F, Porro M, Rossi G, Giaccnne G, Bird TD, Dlouhy SR, Young K, Piccardo P, Ghetti B, Bugiani O, Frangione B. ONLY MUTANT PRP PARTICIPATES IN AMYLOID FORMATION IN GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE WITH ALA>VAL SUBSTITUTION AT CODON 117 Journal of Neuropathology and Experimental Neurology. 54: 416. DOI: 10.1097/00005072-199505000-00037  0.402
1994 Tagliavini F, Prelli F, Porro M, Rossi G, Giaccone G, Farlow MR, Dlouhy SR, Ghetti B, Bugiani O, Frangione B. Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele. Cell. 79: 695-703. PMID 7954833 DOI: 10.1016/0092-8674(94)90554-1  0.445
1994 Ghetti B, Tagliavini F, Giaccone G, Bugiani O, Frangione B, Farlow MR, Dlouhy SR. Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles. Molecular Neurobiology. 8: 41-8. PMID 7916191 DOI: 10.1007/Bf02778006  0.304
1994 Bugiani O, Giaccone G, Frigerio L, Farlow M, Ghetti B, Tagliavini F. Apolipoprotein E and J immunoreactivity in Gerstmann-Sträussler-Scheinker disease Neurobiology of Aging. 15: S156-S157. DOI: 10.1016/0197-4580(94)93095-3  0.311
1994 Forloni G, Chiesa R, Bo RD, Angeretti N, Lucca E, Salmona M, Bugiani O, Tagliavini F. Neurodegenerative effects induced by β-amyloid and PRP peptides: Similarities and differences Neurobiology of Aging. 15. DOI: 10.1016/0197-4580(94)92809-6  0.331
1993 Forloni G, Angeretti N, Chiesa R, Monzani E, Salmona M, Bugiani O, Tagliavini F. Neurotoxicity of a prion protein fragment. Nature. 362: 543-6. PMID 8464494 DOI: 10.1038/362543A0  0.396
1993 Tagliavini F, Giaccone G, Bugiani O, Frangione B. Ubiquitinated neurites are associated with preamyloid and cerebral amyloid beta deposits in patients with hereditary cerebral hemorrhage with amyloidosis Dutch type. Acta Neuropathologica. 85: 267-71. PMID 8384771 DOI: 10.1007/Bf00227721  0.409
1993 Tagliavini F, Giaccone G, Prelli F, Verga L, Porro M, Trojanowski JQ, Farlow MR, Frangione B, Ghetti B, Bugiani O. A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindred. Brain Research. 616: 325-9. PMID 8358624 DOI: 10.1016/0006-8993(93)90226-D  0.397
1993 Bugiani O, Giaccone G, Verga L, Pollo B, Frangione B, Farlow MR, Tagliavini F, Ghetti B. Beta PP participates in PrP-amyloid plaques of Gerstmann-Sträussler-Scheinker disease, Indiana kindred. Journal of Neuropathology and Experimental Neurology. 52: 64-70. PMID 8093899 DOI: 10.1097/00005072-199301000-00008  0.391
1993 Tagliavinl F, Angerettti N, Chiesa R, Salmona M, Bugiani O, Forloni G. IN VITRO NEUROTOXICITY OF A FRAGMENT OF THE PRION PROTEIN Journal of Neuropathology and Experimental Neurology. 52: 293. DOI: 10.1097/00005072-199305000-00130  0.312
1993 Giaccone G, Verga L, Bugiani O, Frangione B, Serban D, Prusiner SB, Farlow MR, Ghetti B, Tagliavini F. Corrections: 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. 90: 362. DOI: 10.1073/Pnas.90.1.362B  0.447
1992 Tagliavini F, Prelli F, Porro M, Salmona M, Bugiani O, Frangione B. A soluble form of prion protein in human cerebrospinal fluid: implications for prion-related encephalopathies. Biochemical and Biophysical Research Communications. 184: 1398-404. PMID 1375461 DOI: 10.1016/S0006-291X(05)80038-5  0.347
1992 Giaccone G, Verga L, Bugiani O, Frangione B, Serban D, Prusiner SB, Farlow MR, Ghetti B, Tagliavini F. Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred. Proceedings of the National Academy of Sciences of the United States of America. 89: 9349-53. PMID 1357663 DOI: 10.1073/Pnas.89.19.9349  0.451
1992 Verga L, Giaccone G, Salmona M, Prelli F, Frangione B, Bugiani O, Tagllavini F. Animal and cellular modelsSinthetic peptides homologous to prion protein fragments form amyloid-like fibrils in vitro Neurobiology of Aging. 13. DOI: 10.1016/0197-4580(92)90535-6  0.374
1992 Tagliavini F, Prelli F, Porro M, Salmona M, Bugiani O, Frangione B. A soluble form of prion protein in human cerebrospinal fluid as a potential source of PRP amyloid Neurobiology of Aging. 13: S92. DOI: 10.1016/0197-4580(92)90490-O  0.33
1992 Giaccone G, Verga L, Bugiani O, Frangione B, Serban D, Prusiner SB, Farlow MR, Ghetti B, Tagliavini F. Pathology, structural and biochemicalPrion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred☆ Neurobiology of Aging. 13. DOI: 10.1016/0197-4580(92)90282-3  0.437
1992 Farlow M, Bugiani O, Giaccone G, Tagliavini F, Ghetti B, Dlouhy S. A “presymptomatic” case of Gerstmann-Sträussler-Scheinker disease from the indiana kindred has cerebellar deposits of prion protein amyloid and a mutation in the prion protein gene Neurobiology of Aging. 13: S39. DOI: 10.1016/0197-4580(92)90281-2  0.426
1991 el Hachimi KH, Verga L, Giaccone G, Tagliavini F, Frangione B, Bugiani O, Foncin JF. Relationship between non-fibrillary amyloid precursors and cell processes in the cortical neuropil of Alzheimer patients. Neuroscience Letters. 129: 119-22. PMID 1922961 DOI: 10.1016/0304-3940(91)90734-B  0.374
1991 Tagliavini F, Giaccone G, Verga L, Ghiso J, Frangione B, Bugiani O. Alzheimer patients: preamyloid deposits are immunoreactive with antibodies to extracellular domains of the amyloid precursor protein. Neuroscience Letters. 128: 117-20. PMID 1922939 DOI: 10.1016/0304-3940(91)90773-M  0.389
1991 Bugiani O, Tagliavini F, Giaccone G. Preamyloid deposits, amyloid deposits, and senile plaques in Alzheimer's disease, Down syndrome, and aging. Annals of the New York Academy of Sciences. 640: 122-8. PMID 1837976 DOI: 10.1111/J.1749-6632.1991.Tb00203.X  0.408
1991 Tagliavini F, Prelli F, Ghiso J, Bugiani O, Serban D, Prusiner SB, Farlow MR, Ghetti B, Frangione B. Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58. The Embo Journal. 10: 513-9. PMID 1672107 DOI: 10.1002/J.1460-2075.1991.Tb07977.X  0.475
1990 Giaccone G, Verga L, Finazzi M, Pollo B, Tagliavini F, Frangione B, Bugiani O. Cerebral preamyloid deposits and congophilic angiopathy in aged dogs. Neuroscience Letters. 114: 178-83. PMID 2395530 DOI: 10.1016/0304-3940(90)90068-K  0.393
1990 Giaccone G, Tagliavini F, Verga L, Frangione B, Farlow MR, Bugiani O, Ghetti B. Neurofibrillary tangles of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease share antigenic determinants with those of Alzheimer disease. Brain Research. 530: 325-9. PMID 2176119 DOI: 10.1016/0006-8993(90)91304-Y  0.416
1990 Bugiani O, Giaccone G, Verga L, Pollo B, Ghetti B, Frangione B, Tagliavini F. Alzheimer patients and Down patients: abnormal presynaptic terminals are related to cerebral preamyloid deposits. Neuroscience Letters. 119: 56-9. PMID 1965862 DOI: 10.1016/0304-3940(90)90754-W  0.43
1990 Tagliavini F, Ghiso J, Timmers WF, Giaccone G, Bugiani O, Frangione B. ALZHEIMERʼS DISEASE AND HEREDITARY (DUTCH-TYPE) CEREBRAL HEMORRHAGE Journal of Neuropathology and Experimental Neurology. 49: 332. DOI: 10.1097/00005072-199005000-00219  0.348
1989 Tagliavini F, Giaccone G, Linoli G, Frangione B, Bugiani O. Cerebral extracellular preamyloid deposits in Alzheimer's disease, Down syndrome and nondemented elderly individuals. Progress in Clinical and Biological Research. 317: 1001-5. PMID 2532368  0.344
1989 Verga L, Frangione B, Tagliavini F, Giaccone G, Migheli A, Bugiani O. Alzheimer patients and Down patients: cerebral preamyloid deposits differ ultrastructurally and histochemically from the amyloid of senile plaques. Neuroscience Letters. 105: 294-9. PMID 2531851 DOI: 10.1016/0304-3940(89)90636-8  0.417
1989 Giaccone G, Tagliavini F, Linoli G, Bouras C, Frigerio L, Frangione B, Bugiani O. Down patients: extracellular preamyloid deposits precede neuritic degeneration and senile plaques. Neuroscience Letters. 97: 232-8. PMID 2521927 DOI: 10.1016/0304-3940(89)90169-9  0.426
1989 Bugiani O, Giaccone G, Frangione B, Ghetti B, Tagliavini F. Alzheimer patients: preamyloid deposits are more widely distributed than senile plaques throughout the central nervous system. Neuroscience Letters. 103: 263-8. PMID 2478933 DOI: 10.1016/0304-3940(89)90110-9  0.424
1988 Tagliavini F, Giaccone G, Frangione B, Bugiani O. Preamyloid deposits in the cerebral cortex of patients with Alzheimer's disease and nondemented individuals. Neuroscience Letters. 93: 191-6. PMID 3241644 DOI: 10.1016/0304-3940(88)90080-8  0.432
1988 TAGLIAVINI F, GIACCONE G, LINOLI G, FRANGIONE B, BUGIANI O. PREAMYLOID DEPOSITS PRECEDE SENILE PLAQUE FORMATION IN THE DEVELOPMENT OF ALZHEIMER CHANGES IN DOWN SYNDROME Alzheimer Disease & Associated Disorders. 2: 405. DOI: 10.1097/00002093-198802040-00035  0.352
1987 Bugiani O, Tagliavini F, Giaccone G. ASTROCYTOSIS AND SPONGIFORM CHANGES OF THE WHITE MATTER IN CREUTZFELDT-JAKOB DISEASE (CJ) Journal of Neuropathology and Experimental Neurology. 46: 387. DOI: 10.1097/00005072-198705000-00174  0.322
1986 Tagliavini F, Bouras C, Ghetti B, Constantinidis J, Bugiani O. ALZHEIMERʼS DISEASE (AD) Journal of Neuropathology and Experimental Neurology. 45: 361. DOI: 10.1097/00005072-198605000-00141  0.363
1986 Bugiani O, Constantinidis J, Ghetti B, Bouras C, Tagliavini F. ASYMMETRIC CEREBRAL ATROPHY IN ALZHEIMERʼS DISEASE Journal of Neuropathology and Experimental Neurology. 45: 342. DOI: 10.1097/00005072-198605000-00086  0.362
1984 Bugiani O, Tabaton M, Cammarata S. Huntington's disease: survival of large striatal neurons in the rigid variant. Annals of Neurology. 15: 154-6. PMID 6230987 DOI: 10.1002/Ana.410150207  0.312
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