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Items: 1 to 50 of 184

1.

Review: PrP 106-126 - 25 years after.

Forloni G, Chiesa R, Bugiani O, Salmona M, Tagliavini F.

Neuropathol Appl Neurobiol. 2019 Jan 12. doi: 10.1111/nan.12538. [Epub ahead of print] Review.

PMID:
30635947
2.

Neuro-Behçet's disease presenting as an isolated progressive cognitive and behavioral syndrome.

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.

Neurocase. 2018 Dec 25:1-4. doi: 10.1080/13554794.2018.1561898. [Epub ahead of print]

PMID:
30583716
3.

An In Vivo 11C-(R)-PK11195 PET and In Vitro Pathology Study of Microglia Activation in Creutzfeldt-Jakob Disease.

Iaccarino L, Moresco RM, Presotto L, Bugiani O, Iannaccone S, Giaccone G, Tagliavini F, Perani D.

Mol Neurobiol. 2018 Apr;55(4):2856-2868. doi: 10.1007/s12035-017-0522-6. Epub 2017 Apr 28.

PMID:
28455699
4.

Erratum to: Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium.

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, Ironside JW, Kavantzas N, King A, Korkolopoulou P, Kovács GG, Meyronet D, Monoranu C, Nilsson T, Parchi P, Patsouris E, Revesz T, Roggendorf W, Rozemuller A, Seilhean D, Streichenberger N, Thal DR, Wharton SB, Kretzschmar H.

J Neural Transm (Vienna). 2015 Jul;122(7):973-4. doi: 10.1007/s00702-014-1337-5. No abstract available.

PMID:
25418279
5.

Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium.

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, Ironside JW, Kavantzas N, King A, Korkolopoulou P, Kovács GG, Meyronet D, Monoranu C, Nilsson T, Parchi P, Patsouris E, Revesz T, Roggendorf W, Rozemuller A, Seilhean D, Streichenberger N, Thal DR, Wharton SB, Kretzschmar H.

J Neural Transm (Vienna). 2015 Jul;122(7):957-72. doi: 10.1007/s00702-014-1304-1. Epub 2014 Sep 20. Erratum in: J Neural Transm (Vienna). 2015 Jul;122(7):973-4.

6.

A mutation in the 5'-UTR of GRN gene associated with frontotemporal lobar degeneration: phenotypic variability and possible pathogenetic mechanisms.

Puoti G, Lerza MC, Ferretti MG, Bugiani O, Tagliavini F, Rossi G.

J Alzheimers Dis. 2014;42(3):939-47. doi: 10.3233/JAD-140717.

PMID:
25024321
7.

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

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, Tagliavini F.

Acta Neuropathol. 2012 Dec;124(6):809-21. doi: 10.1007/s00401-012-1061-x. Epub 2012 Nov 13. Erratum in: Acta Neuropathol. 2013 Mar;125(3):467.

PMID:
23143229
8.

A case of multiple sclerosis with pure, massive superficial demyelination.

Giaccone G, Bugiani O, Ferrero P, Orsi L, Tagliavini F.

Neurology. 2012 Jul 24;79(4):384-6. doi: 10.1212/WNL.0b013e31826043c2. Epub 2012 Jul 11. No abstract available.

PMID:
22786593
9.

The need to unify neuropathological assessments of vascular alterations in the ageing brain: multicentre survey by the BrainNet Europe consortium.

Alafuzoff I, Gelpi E, Al-Sarraj S, Arzberger T, Attems J, Bodi I, Bogdanovic N, Budka H, Bugiani O, Englund E, Ferrer I, Gentleman S, Giaccone G, Graeber MB, Hortobagyi T, Höftberger R, Ironside JW, Jellinger K, Kavantzas N, King A, Korkolopoulou P, Kovács GG, Meyronet D, Monoranu C, Parchi P, Patsouris E, Roggendorf W, Rozemuller A, Seilhean D, Streichenberger N, Thal DR, Wharton SB, Kretzschmar H.

Exp Gerontol. 2012 Nov;47(11):825-33. doi: 10.1016/j.exger.2012.06.001. Epub 2012 Jun 15.

PMID:
22705312
10.

Alzheimer's disease: ageing-related or age-related? New hypotheses from an old debate.

Bugiani O.

Neurol Sci. 2011 Dec;32(6):1241-7. doi: 10.1007/s10072-011-0614-4. Epub 2011 May 13.

PMID:
21567180
11.

A novel pathogenic PSEN1 mutation in a family with Alzheimer's disease: phenotypical and neuropathological features.

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, Maletta R, Ghidoni E, Bugiani O, Tagliavini F, Giaccone G, Bruni AC.

J Alzheimers Dis. 2011;25(3):425-31. doi: 10.3233/JAD-2011-110185.

PMID:
21422519
12.

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

Bellucci A, Bugiani O, Ghetti B, Spillantini MG.

Neurodegener Dis. 2011;8(4):221-9. doi: 10.1159/000322228. Epub 2011 Jan 5.

13.

Myoclonus in Creutzfeldt-Jakob disease: polygraphic and video-electroencephalography assessment of 109 patients.

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.

Mov Disord. 2010 Dec 15;25(16):2818-27. doi: 10.1002/mds.23397.

PMID:
20939057
14.

Low-voltage bilateral pallidal stimulation for severe meige syndrome in a patient with primary segmental dystonia: case report.

Romito LM, Elia AE, Franzini A, Bugiani O, Albanese A.

Neurosurgery. 2010 Sep;67(3 Suppl Operative):onsE308; discussion onsE308. doi: 10.1227/01.NEU.0000381768.04640.46.

PMID:
20729656
15.

Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP.

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, Romorini A, Patruno GM, Magoni M, Padovani A, Tagliavini F.

Arch Neurol. 2010 Aug;67(8):987-95. doi: 10.1001/archneurol.2010.178.

PMID:
20697050
16.

Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation.

Bruni AC, Bernardi L, Colao R, Rubino E, Smirne N, Frangipane F, Terni B, Curcio SA, Mirabelli M, Clodomiro A, Di Lorenzo R, Maletta R, Anfossi M, Gallo M, Geracitano S, Tomaino C, Muraca MG, Leotta A, Lio SG, Pinessi L, Rainero I, Sorbi S, Nee L, Milan G, Pappatà S, Postiglione A, Abbamondi N, Forloni G, St George Hyslop P, Rogaeva E, Bugiani O, Giaccone G, Foncin JF, Spillantini MG, Puccio G.

Neurology. 2010 Mar 9;74(10):798-806. doi: 10.1212/WNL.0b013e3181d52785. Epub 2010 Feb 17.

17.

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

Cupidi C, Capobianco R, Goffredo D, Marcon G, Ghetti B, Bugiani O, Tagliavini F, Giaccone G.

J Alzheimers Dis. 2010;19(1):57-68. doi: 10.3233/JAD-2010-1205.

PMID:
20061626
18.

Staging/typing of Lewy body related alpha-synuclein pathology: a study of the BrainNet Europe Consortium.

Alafuzoff I, Ince PG, Arzberger T, Al-Sarraj S, Bell J, Bodi I, Bogdanovic N, Bugiani O, Ferrer I, Gelpi E, Gentleman S, Giaccone G, Ironside JW, Kavantzas N, King A, Korkolopoulou P, Kovács GG, Meyronet D, Monoranu C, Parchi P, Parkkinen L, Patsouris E, Roggendorf W, Rozemuller A, Stadelmann-Nessler C, Streichenberger N, Thal DR, Kretzschmar H.

Acta Neuropathol. 2009 Jun;117(6):635-52. doi: 10.1007/s00401-009-0523-2. Epub 2009 Mar 28.

PMID:
19330340
19.

Assessment of beta-amyloid deposits in human brain: a study of the BrainNet Europe Consortium.

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, Ince P, Ironside JW, Kavantzas N, King A, Korkolopoulou P, Kovács GG, Meyronet D, Monoranu C, Nilsson T, Parchi P, Patsouris E, Pikkarainen M, Revesz T, Rozemuller A, Seilhean D, Schulz-Schaeffer W, Streichenberger N, Wharton SB, Kretzschmar H.

Acta Neuropathol. 2009 Mar;117(3):309-20. doi: 10.1007/s00401-009-0485-4. Epub 2009 Feb 1.

20.

A novel phenotype of sporadic Creutzfeldt-Jakob disease.

Giaccone G, Di Fede G, Mangieri M, Limido L, Capobianco R, Suardi S, Grisoli M, Binelli S, Fociani P, Bugiani O, Tagliavini F.

BMJ Case Rep. 2009;2009. pii: bcr09.2008.0945. doi: 10.1136/bcr.09.2008.0945. Epub 2009 Feb 2.

21.

Hamilton rating scale for depression-21 modifications in patients with vagal nerve stimulation for treatment of treatment-resistant depression: series report.

Franzini A, Messina G, Marras C, Savino M, Miniati M, Bugiani O, Broggi G.

Neuromodulation. 2008 Oct;11(4):267-71. doi: 10.1111/j.1525-1403.2008.00174.x.

PMID:
22151139
22.

Staging of neurofibrillary pathology in Alzheimer's disease: a study of the BrainNet Europe Consortium.

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, Korkolopoulou P, Kovács GG, Larionov S, Meyronet D, Monoranu C, Parchi P, Patsouris E, Roggendorf W, Seilhean D, Tagliavini F, Stadelmann C, Streichenberger N, Thal DR, Wharton SB, Kretzschmar H.

Brain Pathol. 2008 Oct;18(4):484-96. doi: 10.1111/j.1750-3639.2008.00147.x. Epub 2008 Mar 26.

23.

Differential neuropsychological patterns of frontal variant frontotemporal dementia and Alzheimer's disease in a study of diagnostic concordance.

Giovagnoli AR, Erbetta A, Reati F, Bugiani O.

Neuropsychologia. 2008 Apr;46(5):1495-504. doi: 10.1016/j.neuropsychologia.2007.12.023. Epub 2008 Jan 5.

PMID:
18262206
24.

A novel phenotype of sporadic Creutzfeldt-Jakob disease.

Giaccone G, Di Fede G, Mangieri M, Limido L, Capobianco R, Suardi S, Grisoli M, Binelli S, Fociani P, Bugiani O, Tagliavini F.

J Neurol Neurosurg Psychiatry. 2007 Dec;78(12):1379-82.

25.

The many ways to frontotemporal degeneration and beyond.

Bugiani O.

Neurol Sci. 2007 Oct;28(5):241-4. Review.

PMID:
17972037
26.

Chronic high frequency stimulation of the posteromedial hypothalamus in facial pain syndromes and behaviour disorders.

Franzini A, Marras C, Tringali G, Leone M, Ferroli P, Bussone G, Bugiani O, Broggi G.

Acta Neurochir Suppl. 2007;97(Pt 2):399-406.

PMID:
17691328
27.

Tauopathy in human and experimental variant Creutzfeldt-Jakob disease.

Giaccone G, Mangieri M, Capobianco R, Limido L, Hauw JJ, Haïk S, Fociani P, Bugiani O, Tagliavini F.

Neurobiol Aging. 2008 Dec;29(12):1864-73. Epub 2007 Jun 8.

PMID:
17560687
28.

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

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, Wszolek ZK.

J Neural Transm (Vienna). 2007 Jul;114(7):947-50. Epub 2007 Feb 23.

PMID:
17318302
29.

Interlaboratory comparison of assessments of Alzheimer disease-related lesions: a study of the BrainNet Europe Consortium.

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, King A, Kopp N, Korkolopoulou P, Kovács GG, Meyronet D, Parchi P, Patsouris E, Preusser M, Ravid R, Roggendorf W, Seilhean D, Streichenberger N, Thal DR, Kretzschmar H.

J Neuropathol Exp Neurol. 2006 Aug;65(8):740-57.

PMID:
16896308
30.

Neuropathology of the dementias other than Alzheimer's.

Bugiani O.

Neurol Sci. 2006 Mar;27 Suppl 1:S44-6. Review.

PMID:
16708184
31.

CT and MR imaging of neuroaxonal leukodystrophy presenting as early-onset frontal dementia.

Mascalchi M, Gavazzi C, Morbin M, Giaccone G, Arnetoli G, Zappoli R, Bugiani O.

AJNR Am J Neuroradiol. 2006 May;27(5):1037-9.

32.

Periodic electroencephalogram complexes in a patient with variant Creutzfeldt-Jakob disease.

Binelli S, Agazzi P, Giaccone G, Will RG, Bugiani O, Franceschetti S, Tagliavini F.

Ann Neurol. 2006 Feb;59(2):423-7.

PMID:
16437565
33.

Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPSc.

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, Tagliavini F.

J Neuropathol Exp Neurol. 2005 Oct;64(10):902-9.

PMID:
16215462
34.

Stimulation of the posterior hypothalamus for medically intractable impulsive and violent behavior.

Franzini A, Marras C, Ferroli P, Bugiani O, Broggi G.

Stereotact Funct Neurosurg. 2005;83(2-3):63-6. Epub 2005 Jun 30.

PMID:
15990469
35.

Familial frontotemporal dementia associated with the novel MAPT mutation T427M.

Giaccone G, Rossi G, Farina L, Marcon G, Di Fede G, Catania M, Morbin M, Sacco L, Bugiani O, Tagliavini F.

J Neurol. 2005 Dec;252(12):1543-5. Epub 2005 Jun 6. No abstract available.

PMID:
15940384
36.

The effect of tau genotype on clinical features in FTDP-17.

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, Delisle MB, Rascol O, Arima K, Dysken MW, Yasuda M, Kobayashi T, Sunohara N, Komure O, Kuno S, Sperfeld AD, Stoppe G, Kohlhase J, Pickering-Brown S, Neary D, Bugiani O, Wszolek ZK.

Parkinsonism Relat Disord. 2005 Jun;11(4):205-8.

PMID:
15878580
37.

Long-term high-frequency bilateral pallidal stimulation for neuroleptic-induced tardive dystonia. Report of two cases.

Franzini A, Marras C, Ferroli P, Zorzi G, Bugiani O, Romito L, Broggi G.

J Neurosurg. 2005 Apr;102(4):721-5.

PMID:
15871516
38.

FVEPs in Creutzfeldt-Jacob disease: waveforms and interaction with the periodic EEG pattern assessed by single sweep analysis.

Visani E, Agazzi P, Scaioli V, Giaccone G, Binelli S, Canafoglia L, Panzica F, Tagliavini F, Bugiani O, Avanzini G, Franceschetti S.

Clin Neurophysiol. 2005 Apr;116(4):895-904. Epub 2005 Jan 13.

PMID:
15792899
39.

A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene.

Rossi G, Giaccone G, Maletta R, Morbin M, Capobianco R, Mangieri M, Giovagnoli AR, Bizzi A, Tomaino C, Perri M, Di Natale M, Tagliavini F, Bugiani O, Bruni AC.

Neurology. 2004 Sep 14;63(5):910-2.

PMID:
15365148
40.

Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 gene.

Marcon G, Giaccone G, Cupidi C, Balestrieri M, Beltrami CA, Finato N, Bergonzi P, Sorbi S, Bugiani O, Tagliavini F.

J Neuropathol Exp Neurol. 2004 Mar;63(3):199-209.

PMID:
15055444
41.

A beta-related cerebral amyloid angiopathy.

Bugiani O.

Neurol Sci. 2004 Mar;25 Suppl 1:S1-2. Review.

PMID:
15045608
42.

Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene.

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.

Neurology. 2003 Nov 11;61(9):1288-91.

PMID:
14610142
43.

A case of dementia parkinsonism resembling progressive supranuclear palsy due to mutation in the tau protein gene.

Soliveri P, Rossi G, Monza D, Tagliavini F, Piacentini S, Albanese A, Bugiani O, Girotti F.

Arch Neurol. 2003 Oct;60(10):1454-6.

PMID:
14568818
44.

Structural properties of Gerstmann-Straussler-Scheinker disease amyloid protein.

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, Forloni G, Tagliavini F.

J Biol Chem. 2003 Nov 28;278(48):48146-53. Epub 2003 Sep 11.

45.

Therapeutic approaches to prion diseases.

Rossi G, Salmona M, Forloni G, Bugiani O, Tagliavini F.

Clin Lab Med. 2003 Mar;23(1):187-208. Review.

PMID:
12733432
46.

Hereditary prion protein amyloidoses.

Ghetti B, Tagliavini F, Takao M, Bugiani O, Piccardo P.

Clin Lab Med. 2003 Mar;23(1):65-85, viii. Review.

PMID:
12733425
47.

Tetracyclines affect prion infectivity.

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, Salmona M, Tagliavini F.

Proc Natl Acad Sci U S A. 2002 Aug 6;99(16):10849-54. Epub 2002 Jul 29.

48.

Preserved semantic access in global amnesia and hippocampal damage.

Giovagnoli AR, Erbetta A, Bugiani O.

Clin Neuropsychol. 2001 Dec;15(4):508-15.

PMID:
11935452
49.

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.

Takao M, Ghetti B, Murrell JR, Unverzagt FW, Giaccone G, Tagliavini F, Bugiani O, Piccardo P, Hulette CM, Crain BJ, Farlow MR, Heyman A.

J Neuropathol Exp Neurol. 2001 Dec;60(12):1137-52.

PMID:
11764087
50.

Studies on peptide fragments of prion proteins.

Tagliavini F, Forloni G, D'Ursi P, Bugiani O, Salmona M.

Adv Protein Chem. 2001;57:171-201. Review. No abstract available.

PMID:
11447690

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