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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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J D Rohrer

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Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2011

Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutationK Alner, H Hyare, S Mead, et al.

Brain Communications|May 23, 2022

A data-driven model of brain volume changes in progressive supranuclear palsyW J Scotton, M Bocchetta, E Todd, et al.

Medrxiv : the Preprint Server for Health Sciences|April 2, 2024

Distinct spatiotemporal atrophy patterns in corticobasal syndrome are associated with different underlying pathologiesW J Scotton, C Shand, E G Todd, et al.

Neurology|November 4, 2009

The heritability and genetics of frontotemporal lobar degenerationJ D Rohrer, R Guerreiro, J Vandrovcova, et al.

Neurology|February 18, 2011

Classification of primary progressive aphasia and its variantsM L Gorno-Tempini, A E Hillis, S Weintraub, et al.

Molecular Psychiatry|October 4, 2018

Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral seriesC Koriath, J Kenny, G Adamson, et al.

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Search research articles

Showing results (11-20 of 16) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 16 results.

Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2011

Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutationK Alner, H Hyare, S Mead, et al.

Brain Communications|May 23, 2022

A data-driven model of brain volume changes in progressive supranuclear palsyW J Scotton, M Bocchetta, E Todd, et al.

Medrxiv : the Preprint Server for Health Sciences|April 2, 2024

Distinct spatiotemporal atrophy patterns in corticobasal syndrome are associated with different underlying pathologiesW J Scotton, C Shand, E G Todd, et al.

Neurology|November 4, 2009

The heritability and genetics of frontotemporal lobar degenerationJ D Rohrer, R Guerreiro, J Vandrovcova, et al.

Neurology|February 18, 2011

Classification of primary progressive aphasia and its variantsM L Gorno-Tempini, A E Hillis, S Weintraub, et al.

Molecular Psychiatry|October 4, 2018

Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral seriesC Koriath, J Kenny, G Adamson, et al.

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