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Page 1
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. Giaccone G, et al. Among authors: grisoli m. J Neurol Neurosurg Psychiatry. 2007 Dec;78(12):1379-82. doi: 10.1136/jnnp.2007.115444. J Neurol Neurosurg Psychiatry. 2007. PMID: 18024694 Free PMC article.
Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau.
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, Ghetti B. Bugiani O, et al. Among authors: grisoli m. J Neuropathol Exp Neurol. 1999 Jun;58(6):667-77. doi: 10.1097/00005072-199906000-00011. J Neuropathol Exp Neurol. 1999. PMID: 10374757
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. Giaccone G, et al. Among authors: grisoli m. BMJ Case Rep. 2009;2009:bcr09.2008.0945. doi: 10.1136/bcr.09.2008.0945. Epub 2009 Feb 2. BMJ Case Rep. 2009. PMID: 21686549 Free PMC article.
Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis.
Rohrer JD, Nicholas JM, Cash DM, van Swieten J, Dopper E, Jiskoot L, van Minkelen R, Rombouts SA, Cardoso MJ, Clegg S, Espak M, Mead S, Thomas DL, De Vita E, Masellis M, Black SE, Freedman M, Keren R, MacIntosh BJ, Rogaeva E, Tang-Wai D, Tartaglia MC, Laforce R Jr, Tagliavini F, Tiraboschi P, Redaelli V, Prioni S, Grisoli M, Borroni B, Padovani A, Galimberti D, Scarpini E, Arighi A, Fumagalli G, Rowe JB, Coyle-Gilchrist I, Graff C, Fallström M, Jelic V, Ståhlbom AK, Andersson C, Thonberg H, Lilius L, Frisoni GB, Pievani M, Bocchetta M, Benussi L, Ghidoni R, Finger E, Sorbi S, Nacmias B, Lombardi G, Polito C, Warren JD, Ourselin S, Fox NC, Rossor MN, Binetti G. Rohrer JD, et al. Among authors: grisoli m. Lancet Neurol. 2015 Mar;14(3):253-62. doi: 10.1016/S1474-4422(14)70324-2. Epub 2015 Feb 4. Lancet Neurol. 2015. PMID: 25662776 Free PMC article.
Alzheimer neuropathology without frontotemporal lobar degeneration hallmarks (TAR DNA-binding protein 43 inclusions) in missense progranulin mutation Cys139Arg.
Redaelli V, Rossi G, Maderna E, Kovacs GG, Piccoli E, Caroppo P, Cacciatore F, Spinello S, Grisoli M, Sozzi G, Salmaggi A, Tagliavini F, Giaccone G. Redaelli V, et al. Among authors: grisoli m. Brain Pathol. 2018 Jan;28(1):72-76. doi: 10.1111/bpa.12480. Epub 2017 Feb 15. Brain Pathol. 2018. PMID: 27997711 Free PMC article.
Cognitive reserve and TMEM106B genotype modulate brain damage in presymptomatic frontotemporal dementia: a GENFI study.
Premi E, Grassi M, van Swieten J, Galimberti D, Graff C, Masellis M, Tartaglia C, Tagliavini F, Rowe JB, Laforce R Jr, Finger E, Frisoni GB, de Mendonça A, Sorbi S, Gazzina S, Cosseddu M, Archetti S, Gasparotti R, Manes M, Alberici A, Cardoso MJ, Bocchetta M, Cash DM, Ourselin S, Padovani A, Rohrer JD, Borroni B; Genetic FTD Initiative (GENFI). Premi E, et al. Brain. 2017 Jun 1;140(6):1784-1791. doi: 10.1093/brain/awx103. Brain. 2017. PMID: 28460069 Free PMC article.
Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome.
Luisa SF, Rizzo A, Bedini G, Capone F, Di Lazzaro V, Nava S, Acerbi F, Rossi DS, Binelli S, Faragò G, Gioppo A, Grisoli M, Bruzzone MG, Ferroli P, Pantaleoni C, Caputi L, Gomez JV, Parati EA, Bersano A. Luisa SF, et al. Among authors: grisoli m. Int J Mol Sci. 2018 Nov 20;19(11):3675. doi: 10.3390/ijms19113675. Int J Mol Sci. 2018. PMID: 30463371 Free PMC article.
113 results