| 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 |
0.396 |
|
| 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 |
0.3 |
|
| 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 |
0.307 |
|
| 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 |
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| 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 |
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| 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 |
0.456 |
|
| 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 |
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| 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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