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Items: 38

1.

Primary Progressive Aphasia: Natural History in an Italian Cohort.

Ferrari C, Polito C, Vannucchi S, Piaceri I, Bagnoli S, Lombardi G, Lucidi G, Berti V, Nacmias B, Sorbi S.

Alzheimer Dis Assoc Disord. 2019 Jan-Mar;33(1):42-46. doi: 10.1097/WAD.0000000000000282.

PMID:
30640256
2.

Crossed aphasia in nonfluent variant of primary progressive aphasia carrying a GRN mutation.

Bessi V, Piaceri I, Padiglioni S, Bagnoli S, Berti V, Sorbi S, Nacmias B.

J Neurol Sci. 2018 Sep 15;392:34-37. doi: 10.1016/j.jns.2018.06.026. Epub 2018 Jun 30. No abstract available.

PMID:
30097151
3.

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.

Pottier C, Zhou X, Perkerson RB 3rd, Baker M, Jenkins GD, Serie DJ, Ghidoni R, Benussi L, Binetti G, López de Munain A, Zulaica M, Moreno F, Le Ber I, Pasquier F, Hannequin D, Sánchez-Valle R, Antonell A, Lladó A, Parsons TM, Finch NA, Finger EC, Lippa CF, Huey ED, Neumann M, Heutink P, Synofzik M, Wilke C, Rissman RA, Slawek J, Sitek E, Johannsen P, Nielsen JE, Ren Y, van Blitterswijk M, DeJesus-Hernandez M, Christopher E, Murray ME, Bieniek KF, Evers BM, Ferrari C, Rollinson S, Richardson A, Scarpini E, Fumagalli GG, Padovani A, Hardy J, Momeni P, Ferrari R, Frangipane F, Maletta R, Anfossi M, Gallo M, Petrucelli L, Suh E, Lopez OL, Wong TH, van Rooij JGJ, Seelaar H, Mead S, Caselli RJ, Reiman EM, Noel Sabbagh M, Kjolby M, Nykjaer A, Karydas AM, Boxer AL, Grinberg LT, Grafman J, Spina S, Oblak A, Mesulam MM, Weintraub S, Geula C, Hodges JR, Piguet O, Brooks WS, Irwin DJ, Trojanowski JQ, Lee EB, Josephs KA, Parisi JE, Ertekin-Taner N, Knopman DS, Nacmias B, Piaceri I, Bagnoli S, Sorbi S, Gearing M, Glass J, Beach TG, Black SE, Masellis M, Rogaeva E, Vonsattel JP, Honig LS, Kofler J, Bruni AC, Snowden J, Mann D, Pickering-Brown S, Diehl-Schmid J, Winkelmann J, Galimberti D, Graff C, Öijerstedt L, Troakes C, Al-Sarraj S, Cruchaga C, Cairns NJ, Rohrer JD, Halliday GM, Kwok JB, van Swieten JC, White CL 3rd, Ghetti B, Murell JR, Mackenzie IRA, Hsiung GR, Borroni B, Rossi G, Tagliavini F, Wszolek ZK, Petersen RC, Bigio EH, Grossman M, Van Deerlin VM, Seeley WW, Miller BL, Graff-Radford NR, Boeve BF, Dickson DW, Biernacka JM, Rademakers R.

Lancet Neurol. 2018 Jun;17(6):548-558. doi: 10.1016/S1474-4422(18)30126-1. Epub 2018 Apr 30.

4.

Biomarkers study in atypical dementia: proof of a diagnostic work-up.

Lombardi G, Polito C, Berti V, Ferrari C, Lucidi G, Bagnoli S, Piaceri I, Nacmias B, Pupi A, Sorbi S.

Neurol Sci. 2018 Jul;39(7):1203-1210. doi: 10.1007/s10072-018-3400-8. Epub 2018 Apr 13.

PMID:
29651720
5.

Novel GRN Mutations in Alzheimer's Disease and Frontotemporal Lobar Degeneration.

Piaceri I, Imperiale D, Ghidoni E, Atzori C, Bagnoli S, Ferrari C, Ungari S, Ambrogio L, Sorbi S, Nacmias B.

J Alzheimers Dis. 2018;62(4):1683-1689. doi: 10.3233/JAD-170989.

PMID:
29614680
6.

Alzheimer's Disease Progression: Factors Influencing Cognitive Decline.

Ferrari C, Lombardi G, Polito C, Lucidi G, Bagnoli S, Piaceri I, Nacmias B, Berti V, Rizzuto D, Fratiglioni L, Sorbi S.

J Alzheimers Dis. 2018;61(2):785-791. doi: 10.3233/JAD-170665.

PMID:
29226870
7.

Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline.

Piaceri I, Bessi V, Matà S, Polito C, Tedde A, Berti V, Bagnoli S, Braccia A, Del Mastio M, Pignone AM, Pupi A, Sorbi S, Nacmias B.

J Alzheimers Dis. 2018;61(1):41-46. doi: 10.3233/JAD-170694.

PMID:
29103041
8.

Genetic Heterogeneity of Alzheimer's Disease: Embracing Research Partnerships.

Nacmias B, Bagnoli S, Piaceri I, Sorbi S.

J Alzheimers Dis. 2018;62(3):903-911. doi: 10.3233/JAD-170570. Review.

9.

Notch4 and mhc class II polymorphisms are associated with hcv-related benign and malignant lymphoproliferative diseases.

Gragnani L, Fognani E, De Re V, Libra M, Garozzo A, Caini P, Cerretelli G, Giovannelli A, Lorini S, Monti M, Bagnoli S, Piaceri I, Zignego AL.

Oncotarget. 2017 May 6;8(42):71528-71535. doi: 10.18632/oncotarget.17655. eCollection 2017 Sep 22.

10.

Low Florbetapir PET Uptake and Normal Aβ1-42 Cerebrospinal Fluid in an APP Ala713Thr Mutation Carrier.

Lombardi G, Berti V, Tedde A, Bagnoli S, Piaceri I, Polito C, Lucidi G, Ferrari C, Ginestroni A, Moretti M, Pupi A, Nacmias B, Sorbi S.

J Alzheimers Dis. 2017;57(3):697-703. doi: 10.3233/JAD-161170.

PMID:
28304299
11.

Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.

Ferrari R, Grassi M, Graziano F, Palluzzi F, Archetti S, Bonomi E, Bruni AC, Maletta RG, Bernardi L, Cupidi C, Colao R, Rainero I, Rubino E, Pinessi L, Galimberti D, Scarpini E, Serpente M, Nacmias B, Piaceri I, Bagnoli S, Rossi G, Giaccone G, Tagliavini F, Benussi L, Binetti G, Ghidoni R, Singleton A, Hardy J, Momeni P, Padovani A, Borroni B.

J Alzheimers Dis. 2017;56(4):1271-1278. doi: 10.3233/JAD-160949.

12.

Analyses of the role of the glucocorticoid receptor gene polymorphism (rs41423247) as a potential moderator in the association between childhood overweight, psychopathology, and clinical outcomes in Eating Disorders patients: A 6 years follow up study.

Castellini G, Lelli L, Tedde A, Piaceri I, Bagnoli S, Lucenteforte E, Sorbi S, Monteleone AM, Hudziak JJ, Nacmias B, Ricca V.

Psychiatry Res. 2016 Sep 30;243:156-60. doi: 10.1016/j.psychres.2016.06.033. Epub 2016 Jun 25.

PMID:
27400218
13.

Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol.

Bocchetta M, Mega A, Bernardi L, Di Maria E, Benussi L, Binetti G, Borroni B, Colao R, Di Fede G, Fostinelli S, Galimberti D, Gennarelli M, Ghidoni R, Piaceri I, Pievani M, Porteri C, Redaelli V, Rossi G, Suardi S, Babiloni C, Scarpini E, Tagliavini F, Padovani A, Nacmias B, Sorbi S, Frisoni GB, Bruni AC; SINdem Collaborators.

J Alzheimers Dis. 2016;51(1):277-91. doi: 10.3233/JAD-150849.

PMID:
26901402
14.

Novel presenilin 1 mutation (Ile408Thr) in an Italian family with late-onset Alzheimer's disease.

Tedde A, Bartoli A, Piaceri I, Ferrara S, Bagnoli S, Serio A, Sorbi S, Nacmias B.

Neurosci Lett. 2016 Jan 1;610:150-3. doi: 10.1016/j.neulet.2015.11.004. Epub 2015 Nov 5.

PMID:
26549787
15.

A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia.

Ferrari R, Grassi M, Salvi E, Borroni B, Palluzzi F, Pepe D, D'Avila F, Padovani A, Archetti S, Rainero I, Rubino E, Pinessi L, Benussi L, Binetti G, Ghidoni R, Galimberti D, Scarpini E, Serpente M, Rossi G, Giaccone G, Tagliavini F, Nacmias B, Piaceri I, Bagnoli S, Bruni AC, Maletta RG, Bernardi L, Postiglione A, Milan G, Franceschi M, Puca AA, Novelli V, Barlassina C, Glorioso N, Manunta P, Singleton A, Cusi D, Hardy J, Momeni P.

Neurobiol Aging. 2015 Oct;36(10):2904.e13-26. doi: 10.1016/j.neurobiolaging.2015.06.005. Epub 2015 Jun 12.

16.

Genetics of Alzheimer's Disease and Frontotemporal Dementia.

Nacmias B, Piaceri I, Bagnoli S, Tedde A, Piacentini S, Sorbi S.

Curr Mol Med. 2014;14(8):993-1000. doi: 10.2174/1566524014666141010152143.

PMID:
25323872
17.

Epigenetic modifications in Alzheimer's disease: cause or effect?

Piaceri I, Raspanti B, Tedde A, Bagnoli S, Sorbi S, Nacmias B.

J Alzheimers Dis. 2015;43(4):1169-73. doi: 10.3233/JAD-141452.

PMID:
25159670
18.

Frontotemporal dementia and its subtypes: a genome-wide association study.

Ferrari R, Hernandez DG, Nalls MA, Rohrer JD, Ramasamy A, Kwok JB, Dobson-Stone C, Brooks WS, Schofield PR, Halliday GM, Hodges JR, Piguet O, Bartley L, Thompson E, Haan E, Hernández I, Ruiz A, Boada M, Borroni B, Padovani A, Cruchaga C, Cairns NJ, Benussi L, Binetti G, Ghidoni R, Forloni G, Galimberti D, Fenoglio C, Serpente M, Scarpini E, Clarimón J, Lleó A, Blesa R, Waldö ML, Nilsson K, Nilsson C, Mackenzie IR, Hsiung GY, Mann DM, Grafman J, Morris CM, Attems J, Griffiths TD, McKeith IG, Thomas AJ, Pietrini P, Huey ED, Wassermann EM, Baborie A, Jaros E, Tierney MC, Pastor P, Razquin C, Ortega-Cubero S, Alonso E, Perneczky R, Diehl-Schmid J, Alexopoulos P, Kurz A, Rainero I, Rubino E, Pinessi L, Rogaeva E, St George-Hyslop P, Rossi G, Tagliavini F, Giaccone G, Rowe JB, Schlachetzki JC, Uphill J, Collinge J, Mead S, Danek A, Van Deerlin VM, Grossman M, Trojanowski JQ, van der Zee J, Deschamps W, Van Langenhove T, Cruts M, Van Broeckhoven C, Cappa SF, Le Ber I, Hannequin D, Golfier V, Vercelletto M, Brice A, Nacmias B, Sorbi S, Bagnoli S, Piaceri I, Nielsen JE, Hjermind LE, Riemenschneider M, Mayhaus M, Ibach B, Gasparoni G, Pichler S, Gu W, Rossor MN, Fox NC, Warren JD, Spillantini MG, Morris HR, Rizzu P, Heutink P, Snowden JS, Rollinson S, Richardson A, Gerhard A, Bruni AC, Maletta R, Frangipane F, Cupidi C, Bernardi L, Anfossi M, Gallo M, Conidi ME, Smirne N, Rademakers R, Baker M, Dickson DW, Graff-Radford NR, Petersen RC, Knopman D, Josephs KA, Boeve BF, Parisi JE, Seeley WW, Miller BL, Karydas AM, Rosen H, van Swieten JC, Dopper EG, Seelaar H, Pijnenburg YA, Scheltens P, Logroscino G, Capozzo R, Novelli V, Puca AA, Franceschi M, Postiglione A, Milan G, Sorrentino P, Kristiansen M, Chiang HH, Graff C, Pasquier F, Rollin A, Deramecourt V, Lebert F, Kapogiannis D, Ferrucci L, Pickering-Brown S, Singleton AB, Hardy J, Momeni P.

Lancet Neurol. 2014 Jul;13(7):686-99. doi: 10.1016/S1474-4422(14)70065-1.

19.

Advances in imaging-genetic relationships for Alzheimer's disease: clinical implications.

Bagnoli S, Piaceri I, Sorbi S, Nacmias B.

Neurodegener Dis Manag. 2014;4(1):73-81. doi: 10.2217/nmt.13.68. Review.

PMID:
24640981
20.

Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration.

Piaceri I, Pradella S, Cupidi C, Nannucci S, Polito C, Bagnoli S, Tedde A, Smirne N, Anfossi M, Gallo M, Bernardi L, Colao R, Maletta R, Bruni AC, Sorbi S, Nacmias B.

J Alzheimers Dis. 2014;40(3):679-85. doi: 10.3233/JAD-132126.

PMID:
24503614
21.

Heterozygous TREM2 mutations in frontotemporal dementia.

Borroni B, Ferrari F, Galimberti D, Nacmias B, Barone C, Bagnoli S, Fenoglio C, Piaceri I, Archetti S, Bonvicini C, Gennarelli M, Turla M, Scarpini E, Sorbi S, Padovani A.

Neurobiol Aging. 2014 Apr;35(4):934.e7-10. doi: 10.1016/j.neurobiolaging.2013.09.017. Epub 2013 Oct 16.

22.

Imaging and cognitive reserve studies predict dementia in presymptomatic Alzheimer's disease subjects.

Ferrari C, Nacmias B, Bagnoli S, Piaceri I, Lombardi G, Pradella S, Tedde A, Sorbi S.

Neurodegener Dis. 2014;13(2-3):157-9. doi: 10.1159/000353690. Epub 2013 Aug 7. Review.

PMID:
23942061
23.

TOMM40 polymorphisms in Italian Alzheimer's disease and frontotemporal dementia patients.

Bagnoli S, Piaceri I, Tedde A, Bessi V, Bracco L, Sorbi S, Nacmias B.

Neurol Sci. 2013 Jun;34(6):995-8. doi: 10.1007/s10072-013-1425-6. Epub 2013 Apr 2.

PMID:
23546992
24.

Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation.

Galimberti D, Fenoglio C, Serpente M, Villa C, Bonsi R, Arighi A, Fumagalli GG, Del Bo R, Bruni AC, Anfossi M, Clodomiro A, Cupidi C, Nacmias B, Sorbi S, Piaceri I, Bagnoli S, Bessi V, Marcone A, Cerami C, Cappa SF, Filippi M, Agosta F, Magnani G, Comi G, Franceschi M, Rainero I, Giordana MT, Rubino E, Ferrero P, Rogaeva E, Xi Z, Confaloni A, Piscopo P, Bruno G, Talarico G, Cagnin A, Clerici F, Dell'Osso B, Comi GP, Altamura AC, Mariani C, Scarpini E.

Biol Psychiatry. 2013 Sep 1;74(5):384-91. doi: 10.1016/j.biopsych.2013.01.031. Epub 2013 Mar 7.

25.

Genetics of familial and sporadic Alzheimer's disease.

Piaceri I, Nacmias B, Sorbi S.

Front Biosci (Elite Ed). 2013 Jan 1;5:167-77. Review.

PMID:
23276979
26.

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats.

van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theuns J, Engelborghs S, Philtjens S, Vandenbulcke M, Sleegers K, Sieben A, Bäumer V, Maes G, Corsmit E, Borroni B, Padovani A, Archetti S, Perneczky R, Diehl-Schmid J, de Mendonça A, Miltenberger-Miltenyi G, Pereira S, Pimentel J, Nacmias B, Bagnoli S, Sorbi S, Graff C, Chiang HH, Westerlund M, Sanchez-Valle R, Llado A, Gelpi E, Santana I, Almeida MR, Santiago B, Frisoni G, Zanetti O, Bonvicini C, Synofzik M, Maetzler W, Vom Hagen JM, Schöls L, Heneka MT, Jessen F, Matej R, Parobkova E, Kovacs GG, Ströbel T, Sarafov S, Tournev I, Jordanova A, Danek A, Arzberger T, Fabrizi GM, Testi S, Salmon E, Santens P, Martin JJ, Cras P, Vandenberghe R, De Deyn PP, Cruts M, Van Broeckhoven C, van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theuns J, Philtjens S, Sleegers K, Bäumer V, Maes G, Corsmit E, Cruts M, Van Broeckhoven C, van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Philtjens S, Theuns J, Sleegers K, Bäumer V, Maes G, Cruts M, Van Broeckhoven C, Engelborghs S, De Deyn PP, Cras P, Engelborghs S, De Deyn PP, Vandenbulcke M, Vandenbulcke M, Borroni B, Padovani A, Archetti S, Perneczky R, Diehl-Schmid J, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, de Mendonça A, Miltenberger-Miltenyi G, Pereira S, Firmo C, Pimentel J, Sanchez-Valle R, Llado A, Antonell A, Molinuevo J, Gelpi E, Graff C, Chiang HH, Westerlund M, Graff C, Kinhult Ståhlbom A, Thonberg H, Nennesmo I, Börjesson-Hanson A, Nacmias B, Bagnoli S, Sorbi S, Bessi V, Piaceri I, Santana I, Santiago B, Santana I, Helena Ribeiro M, Rosário Almeida M, Oliveira C, Massano J, Garret C, Pires P, Frisoni G, Zanetti O, Bonvicini C, Sarafov S, Tournev I, Jordanova A, Tournev I, Kovacs GG, Ströbel T, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, Jessen F, Matej R, Parobkova E, Danel A, Arzberger T, Maria Fabrizi G, Testi S, Ferrari S, Cavallaro T, Salmon E, Santens P, Cras P; European Early-Onset Dementia Consortium.

Hum Mutat. 2013 Feb;34(2):363-73. doi: 10.1002/humu.22244. Epub 2013 Jan 4.

27.

Ataxia-telangiectasia mutated (ATM) genetic variant in Italian centenarians.

Piaceri I, Bagnoli S, Tedde A, Sorbi S, Nacmias B.

Neurol Sci. 2013 Apr;34(4):573-5. doi: 10.1007/s10072-012-1188-5. Epub 2012 Sep 9.

PMID:
22960875
28.

DAPK1 is associated with FTD and not with Alzheimer's disease.

Tedde A, Piaceri I, Bagnoli S, Lucenteforte E, Piacentini S, Sorbi S, Nacmias B.

J Alzheimers Dis. 2012;32(1):13-7.

PMID:
22785394
29.

Suitability of neuropsychological tests in patients with vascular dementia (VaD).

Bagnoli S, Failli Y, Piaceri I, Rinnoci V, Bessi V, Tedde A, Nacmias B, Sorbi S.

J Neurol Sci. 2012 Nov 15;322(1-2):41-5. doi: 10.1016/j.jns.2012.05.045. Epub 2012 Jun 12. Review.

PMID:
22694976
30.

Mitochondria and Alzheimer's disease.

Piaceri I, Rinnoci V, Bagnoli S, Failli Y, Sorbi S.

J Neurol Sci. 2012 Nov 15;322(1-2):31-4. doi: 10.1016/j.jns.2012.05.033. Epub 2012 Jun 12. Review.

PMID:
22694975
31.

Folate, homocysteine, vitamin B12, and polymorphisms of genes participating in one-carbon metabolism in late-onset Alzheimer's disease patients and healthy controls.

Coppedè F, Tannorella P, Pezzini I, Migheli F, Ricci G, Caldarazzo lenco E, Piaceri I, Polini A, Nacmias B, Monzani F, Sorbi S, Siciliano G, Migliore L.

Antioxid Redox Signal. 2012 Jul 15;17(2):195-204. doi: 10.1089/ars.2011.4368. Epub 2011 Dec 15.

PMID:
22034983
32.

Progranulin genetic screening in frontotemporal lobar degeneration patients from central Italy.

Bagnoli S, Piaceri I, Tedde A, Piacentini S, Nannucci S, Bracco L, Sorbi S, Nacmias B.

Cell Mol Neurobiol. 2012 Jan;32(1):13-6. doi: 10.1007/s10571-011-9741-y. Epub 2011 Jul 29.

PMID:
21800185
33.

Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis.

Piaceri I, Del Mastio M, Tedde A, Bagnoli S, Latorraca S, Massaro F, Paganini M, Corrado A, Sorbi S, Nacmias B.

Clin Genet. 2012 Jul;82(1):83-7. doi: 10.1111/j.1399-0004.2011.01726.x. Epub 2011 Jun 30.

PMID:
21651514
34.

Association Study of Genetic Variants in CDKN2A/CDKN2B Genes/Loci with Late-Onset Alzheimer's Disease.

Tedde A, Piaceri I, Bagnoli S, Lucenteforte E, Ueberham U, Arendt T, Sorbi S, Nacmias B.

Int J Alzheimers Dis. 2011 Apr 14;2011:374631. doi: 10.4061/2011/374631.

35.

Implication of a genetic variant at PICALM in Alzheimer’s disease patients and centenarians.

Piaceri I, Bagnoli S, Lucenteforte E, Mancuso M, Tedde A, Siciliano G, Piacentini S, Bracco L, Sorbi S, Nacmias B.

J Alzheimers Dis. 2011;24(3):409-13. doi: 10.3233/JAD-2011-101791.

PMID:
21297266
36.

Different implication of NEDD9 genetic variant in early and late-onset Alzheimer's disease.

Tedde A, Bagnoli S, Piaceri I, Lucenteforte E, Bessi V, Bracco L, Mugelli A, Sorbi S, Nacmias B.

Neurosci Lett. 2010 Jun 25;477(3):121-3. doi: 10.1016/j.neulet.2010.04.046. Epub 2010 Apr 27.

PMID:
20430066
37.

Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease.

Nacmias B, Tedde A, Bagnoli S, Lucenteforte E, Cellini E, Piaceri I, Guarnieri BM, Bessi V, Bracco L, Sorbi S.

J Alzheimers Dis. 2010;20(1):37-41. doi: 10.3233/JAD-2010-1345.

PMID:
20164602
38.

A PALB2 germline mutation associated with hereditary breast cancer in Italy.

Papi L, Putignano AL, Congregati C, Piaceri I, Zanna I, Sera F, Morrone D, Genuardi M, Palli D.

Fam Cancer. 2010 Jun;9(2):181-5. doi: 10.1007/s10689-009-9295-z. Epub 2009 Sep 18.

PMID:
19763884

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