Items where authors include "Spina, S."

Article

Belchikov, N., Hu, W., Fan, L. et al. (27 more authors) (2025) A single-cell, long-read, isoform-resolved case-control study of FTD reveals cell-type-specific and broad splicing dysregulation in human brain. Cell Reports, 44 (9). 116198. ISSN 2211-1247

Romein, C.A., Kırmızıaltın, S., Reshef, R. et al. (24 more authors) (2025) From research proposal to project management. A guide from the Transkribus community on planning and executing workflows for researchers and GLAM-professionals. International Journal of Digital Humanities. ISSN 2524-7832

Gallagher, M. D., Suh, E., Grossman, M. et al. (73 more authors) (2014) TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions. Acta Neuropathologica, 127 (3). pp. 407-418. ISSN 0001-6322

Van Deerlin, V.M., Sleiman, P.M.A., Martinez-Lage, M. et al. (97 more authors) (2010) Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP43 inclusions. Nature Genetics, 42 (3). pp. 234-239. ISSN 1061-4036,

Mackenzie, I.R.A., Neumann, M., Bigio, E.H. et al. (18 more authors) (2010) Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update. Acta Neuropathologica, 119 (1). 1. ISSN 0001-6322