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MRI data-driven algorithm for the diagnosis of behavioural variant frontotemporal dementia.
Manera AL, Dadar M, Van Swieten JC, Borroni B, Sanchez-Valle R, Moreno F, Laforce R Jr, Graff C, Synofzik M, Galimberti D, Rowe JB, Masellis M, Tartaglia MC, Finger E, Vandenberghe R, de Mendonca A, Tagliavini F, Santana I, Butler CR, Gerhard A, Danek A, Levin J, Otto M, Frisoni G, Ghidoni R, Sorbi S, Rohrer JD, Ducharme S, Collins DL; FTLDNI investigators; GENFI Consortium. Manera AL, et al. Among authors: masellis m. J Neurol Neurosurg Psychiatry. 2021 Mar 15:jnnp-2020-324106. doi: 10.1136/jnnp-2020-324106. Online ahead of print. J Neurol Neurosurg Psychiatry. 2021. PMID: 33722819
Intra-familial clinical heterogeneity due to FTLD-U with TDP-43 proteinopathy caused by a novel deletion in progranulin gene (PGRN).
Gabryelewicz T, Masellis M, Berdynski M, Bilbao JM, Rogaeva E, St George-Hyslop P, Barczak A, Czyzewski K, Barcikowska M, Wszolek Z, Black SE, Zekanowski C. Gabryelewicz T, et al. Among authors: masellis m. J Alzheimers Dis. 2010;22(4):1123-33. doi: 10.3233/JAD-2010-101413. J Alzheimers Dis. 2010. PMID: 20930269 Free PMC article.
Early-onset familial Alzheimer's disease (EOFAD).
Wu L, Rosa-Neto P, Hsiung GY, Sadovnick AD, Masellis M, Black SE, Jia J, Gauthier S. Wu L, et al. Among authors: masellis m. Can J Neurol Sci. 2012 Jul;39(4):436-45. doi: 10.1017/s0317167100013949. Can J Neurol Sci. 2012. PMID: 22728850 Review.
361 results