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Jonathan D Rohrer

Showing results (41-50 of 362) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|February 13, 2013
Primary progressive aphasia with parkinsonismKaren M Doherty, Jonathan D Rohrer, Andrew J Lees, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|February 22, 2019
Amygdala subnuclei are differentially affected in the different genetic and pathological forms of frontotemporal dementiaMartina Bocchetta, Juan Eugenio Iglesias, David M Cash, et al.
Alzheimer'S Research & Therapy|January 27, 2015
Imaging endpoints for clinical trials in Alzheimer's diseaseDavid M Cash, Jonathan D Rohrer, Natalie S Ryan, et al.
Journal of Neurology|November 22, 2018
An update on advances in magnetic resonance imaging of multiple system atrophyViorica Chelban, Martina Bocchetta, Sara Hassanein, et al.
Journal of Alzheimer'S Disease : JAD|September 25, 2015
A Novel MAPT Mutation Causing Corticobasal Syndrome Led by Progressive Apraxia of SpeechCharles R Marshall, Rita Guerreiro, Steffi Thust, et al.
Neurobiology of Aging|September 27, 2020
Variable clinical phenotype in TBK1 mutations: case report of a novel mutation causing primary progressive aphasia and review of the literatureImogen J Swift, Martina Bocchetta, Hanya Benotmane, et al.
Neuro-Degenerative Diseases|September 15, 2010
Novel L284R MAPT mutation in a family with an autosomal dominant progressive supranuclear palsy syndromeJonathan D Rohrer, Dominic Paviour, Jana Vandrovcova, et al.
Alzheimer'S Research & Therapy|March 30, 2020
In vivo staging of frontotemporal lobar degeneration TDP-43 type C pathologyMartina Bocchetta, Maria Del Mar Iglesias Espinosa, Tammaryn Lashley, et al.
Neuroimage|August 28, 2020
Automated segmentation of the hypothalamus and associated subunits in brain MRIBenjamin Billot, Martina Bocchetta, Emily Todd, et al.
Human Brain Mapping|November 8, 2019
Thalamic nuclei in frontotemporal dementia: Mediodorsal nucleus involvement is universal but pulvinar atrophy is unique to C9orf72Martina Bocchetta, Juan E Iglesias, Mollie Neason, et al.
Pageof 37

Showing results (41-50 of 362) with videos related to

Sort By:
Pageof 37
Movement Disorders : Official Journal of the Movement Disorder Society|February 13, 2013
Primary progressive aphasia with parkinsonismKaren M Doherty, Jonathan D Rohrer, Andrew J Lees, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|February 22, 2019
Amygdala subnuclei are differentially affected in the different genetic and pathological forms of frontotemporal dementiaMartina Bocchetta, Juan Eugenio Iglesias, David M Cash, et al.
Alzheimer'S Research & Therapy|January 27, 2015
Imaging endpoints for clinical trials in Alzheimer's diseaseDavid M Cash, Jonathan D Rohrer, Natalie S Ryan, et al.
Journal of Neurology|November 22, 2018
An update on advances in magnetic resonance imaging of multiple system atrophyViorica Chelban, Martina Bocchetta, Sara Hassanein, et al.
Journal of Alzheimer'S Disease : JAD|September 25, 2015
A Novel MAPT Mutation Causing Corticobasal Syndrome Led by Progressive Apraxia of SpeechCharles R Marshall, Rita Guerreiro, Steffi Thust, et al.
Neurobiology of Aging|September 27, 2020
Variable clinical phenotype in TBK1 mutations: case report of a novel mutation causing primary progressive aphasia and review of the literatureImogen J Swift, Martina Bocchetta, Hanya Benotmane, et al.
Neuro-Degenerative Diseases|September 15, 2010
Novel L284R MAPT mutation in a family with an autosomal dominant progressive supranuclear palsy syndromeJonathan D Rohrer, Dominic Paviour, Jana Vandrovcova, et al.
Alzheimer'S Research & Therapy|March 30, 2020
In vivo staging of frontotemporal lobar degeneration TDP-43 type C pathologyMartina Bocchetta, Maria Del Mar Iglesias Espinosa, Tammaryn Lashley, et al.
Neuroimage|August 28, 2020
Automated segmentation of the hypothalamus and associated subunits in brain MRIBenjamin Billot, Martina Bocchetta, Emily Todd, et al.
Human Brain Mapping|November 8, 2019
Thalamic nuclei in frontotemporal dementia: Mediodorsal nucleus involvement is universal but pulvinar atrophy is unique to C9orf72Martina Bocchetta, Juan E Iglesias, Mollie Neason, et al.
Pageof 37