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Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutationALNER, K; HYARE, H; FOX, N. C et al.Journal of neurology, neurosurgery and psychiatry. 2012, Vol 83, Num 1, pp 109-114, issn 0022-3050, 6 p.Article

Presymptomatic studies in genetic frontotemporal dementiaROHRER, J. D; WARREN, J. D; FOX, N. C et al.Revue neurologique (Paris). 2013, Vol 169, Num 10, pp 820-824, issn 0035-3787, 5 p.Conference Paper

Tracking progression in frontotemporal lobar degeneration : Serial MRI in semantic dementiaROHRER, J. D; MCNAUGHT, E; FOSTER, J et al.Neurology. 2008, Vol 71, Num 18, pp 1445-1451, issn 0028-3878, 7 p.Article

Measuring disease progression in frontotemporal lobar degeneration: A clinical and MRI studyGORDON, E; ROHRER, J. D; KIM, L. G et al.Neurology. 2010, Vol 74, Num 8, pp 666-673, issn 0028-3878, 8 p.Article

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Classification of primary progressive aphasia and its variantsGORNO-TEMPINI, M. L; HILLIS, A. E; MANES, F et al.Neurology. 2011, Vol 76, Num 11, pp 1006-1014, issn 0028-3878, 9 p.Article

Patterns of cortical thinning in the language variants of frontotemporal lobar degenerationROHRER, J. D; WARREN, J. D; MODAT, M et al.Neurology. 2009, Vol 72, Num 18, pp 1562-1569, issn 0028-3878, 8 p.Article