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17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression.
Le Guennec K, Quenez O, Nicolas G, Wallon D, Rousseau S, Richard AC, Alexander J, Paschou P, Charbonnier C, Bellenguez C, Grenier-Boley B, Lechner D, Bihoreau MT, Olaso R, Boland A, Meyer V, Deleuze JF, Amouyel P, Munter HM, Bourque G, Lathrop M, Frebourg T, Redon R, Letenneur L, Dartigues JF, Martinaud O, Kalev O, Mehrabian S, Traykov L, Ströbel T, Le Ber I, Caroppo P, Epelbaum S, Jonveaux T, Pasquier F, Rollin-Sillaire A, Génin E, Guyant-Maréchal L, Kovacs GG, Lambert JC, Hannequin D, Campion D, Rovelet-Lecrux A. Le Guennec K, et al. Among authors: caroppo p. Mol Psychiatry. 2017 Aug;22(8):1119-1125. doi: 10.1038/mp.2016.226. Epub 2016 Dec 13. Mol Psychiatry. 2017. PMID: 27956742
Corrigendum: PMCA-based detection of prions in the olfactory mucosa of patients with sporadic Creutzfeldt-Jakob disease.
Cazzaniga FA, Bistaffa E, De Luca CMG, Portaleone SM, Catania M, Redaelli V, Tramacere I, Bufano G, Rossi M, Caroppo P, Giovagnoli AR, Tiraboschi P, Di Fede G, Eleopra R, Devigili G, Elia AE, Cilia R, Fiorini M, Bongianni M, Salzano G, Celauro L, Quarta FG, Mammana A, Legname G, Tagliavini F, Parchi P, Zanusso G, Giaccone G, Moda F. Cazzaniga FA, et al. Among authors: caroppo p. Front Aging Neurosci. 2023 Feb 27;15:1073356. doi: 10.3389/fnagi.2023.1073356. eCollection 2023. Front Aging Neurosci. 2023. PMID: 36923119 Free PMC article.
Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia-clinical features and neuroimaging correlates.
Ghirelli A, Spinelli EG, Canu E, Domi T, Basaia S, Castelnovo V, Pozzi L, Magnani G, Caso F, Caroppo P, Prioni S, Villa C, Riva N, Quattrini A, Carrera P, Filippi M, Agosta F. Ghirelli A, et al. Among authors: caroppo p. J Neurol. 2023 Oct;270(10):5102-5109. doi: 10.1007/s00415-023-11839-3. Epub 2023 Jun 29. J Neurol. 2023. PMID: 37382630 Free PMC article. No abstract available.
Functional Connectivity From Disease Epicenters in Frontotemporal Dementia.
Agosta F, Spinelli EG, Basaia S, Cividini C, Falbo F, Pavone C, Riva N, Canu E, Castelnovo V, Magnani G, Caso F, Caroppo P, Prioni S, Villa C, Tremolizzo L, Appollonio I, Silani V, Josephs KA, Whitwell J, Filippi M. Agosta F, et al. Among authors: caroppo p. Neurology. 2023 May 30;100(22):e2290-e2303. doi: 10.1212/WNL.0000000000207277. Epub 2023 Apr 17. Neurology. 2023. PMID: 37068954 Free PMC article.
Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration.
Clot F, Rovelet-Lecrux A, Lamari F, Noël S, Keren B, Camuzat A, Michon A, Jornea L, Laudier B, de Septenville A, Caroppo P, Campion D, Cazeneuve C, Brice A, LeGuern E, Le Ber I; French clinical and genetic research network on FTLD/FTLD-ALS. Clot F, et al. Among authors: caroppo p. Neurogenetics. 2014 May;15(2):95-100. doi: 10.1007/s10048-014-0389-x. Epub 2014 Jan 28. Neurogenetics. 2014. PMID: 24469240
Lateral Temporal Lobe: An Early Imaging Marker of the Presymptomatic GRN Disease?
Caroppo P, Habert MO, Durrleman S, Funkiewiez A, Perlbarg V, Hahn V, Bertin H, Gaubert M, Routier A, Hannequin D, Deramecourt V, Pasquier F, Rivaud-Pechoux S, Vercelletto M, Edouart G, Valabregue R, Lejeune P, Didic M, Corvol JC, Benali H, Lehericy S, Dubois B, Colliot O, Brice A, Le Ber I; Predict-PGRN study group. Caroppo P, et al. J Alzheimers Dis. 2015;47(3):751-9. doi: 10.3233/JAD-150270. J Alzheimers Dis. 2015. PMID: 26401709 Free PMC article.
Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations.
Luis E, Ortiz A, Eudave L, Ortega-Cubero S, Borroni B, van der Zee J, Gazzina S, Caroppo P, Rubino E, D'Agata F, Le Ber I, Santana I, Cunha G, Almeida MR, Boutoleau-Bretonnière C, Hannequin D, Wallon D, Rainero I, Galimberti D, Van Broeckhoven C, Pastor MA, Pastor P. Luis E, et al. Among authors: caroppo p. J Alzheimers Dis. 2016 May 7;53(1):303-13. doi: 10.3233/JAD-160006. J Alzheimers Dis. 2016. PMID: 27163810 Free article.
133 results