Search Results - "Rohrer, J D"

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    Patterns of cortical thinning in the language variants of frontotemporal lobar degeneration by ROHRER, J. D, WARREN, J. D, MODAT, M, RIDGWAY, G. R, DOUIRI, A, ROSSOR, M. N, OURSELIN, S, FOX, N. C

    Published in Neurology (05-05-2009)
    “…Frontotemporal lobar degeneration (FTLD) is a clinically, genetically, and pathologically heterogeneous neurodegenerative disorder. Two subtypes commonly…”
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    Journal Article
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    Classification of primary progressive aphasia and its variants by GORNO-TEMPINI, M. L, HILLIS, A. E, MANES, F, DRONKERS, N. F, VANDENBERGHE, R, RASCOVSKY, K, PATTERSON, K, MILLER, B. L, KNOPMAN, D. S, HODGES, J. R, MESULAM, M. M, GROSSMAN, M, WEINTRAUB, S, KERTESZ, A, MENDEZ, M, CAPPA, S. F, OGAR, J. M, ROHRER, J. D, BLACK, S, BOEVE, B. F

    Published in Neurology (15-03-2011)
    “…This article provides a classification of primary progressive aphasia (PPA) and its 3 main variants to improve the uniformity of case reporting and the…”
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    Journal Article Conference Proceeding
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    The heritability and genetics of frontotemporal lobar degeneration by ROHRER, J. D, GUERREIRO, R, MACKENZIE, I. R. A, WARREN, J. D, DE SILVA, R, HOLTON, J, REVESZ, T, HARDY, J, MEAD, S, ROSSOR, M. N, VANDROVCOVA, J, UPHILL, J, REIMAN, D, BECK, J, ISAACS, A. M, AUTHIER, A, FERRARI, R, FOX, N. C

    Published in Neurology (03-11-2009)
    “…Frontotemporal lobar degeneration (FTLD) is a genetically and pathologically heterogeneous neurodegenerative disorder. We collected blood samples from a cohort…”
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    Journal Article
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    Review: Fluid biomarkers for frontotemporal dementias by Zetterberg, H., van Swieten, J. C., Boxer, A. L., Rohrer, J. D.

    Published in Neuropathology and applied neurobiology (01-02-2019)
    “…Frontotemporal dementias (FTDs) are clinically, genetically and pathologically heterogeneous neurodegenerative disorders that affect the frontal and anterior…”
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    Journal Article
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    TDP-43 subtypes are associated with distinct atrophy patterns in frontotemporal dementia by ROHRER, J. D, GESER, F, ZHOU, J, GENNATAS, E. D, SIDHU, M, TROJANOWSKI, J. Q, DEARMOND, S. J, MILLER, B. L, SEELEY, W. W

    Published in Neurology (14-12-2010)
    “…We sought to describe the antemortem clinical and neuroimaging features among patients with frontotemporal lobar degeneration with TDP-43 immunoreactive…”
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    Journal Article
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    Measuring disease progression in frontotemporal lobar degeneration: A clinical and MRI study by GORDON, E, ROHRER, J. D, KIM, L. G, OMAR, R, ROSSOR, M. N, FOX, N. C, WARREN, J. D

    Published in Neurology (23-02-2010)
    “…There is currently much interest in biomarkers of disease activity in frontotemporal lobar degeneration (FTLD). We assessed MRI and behavioral measures of…”
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    Journal Article
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    Tracking progression in frontotemporal lobar degeneration : Serial MRI in semantic dementia by ROHRER, J. D, MCNAUGHT, E, FOSTER, J, CLEGG, S. L, BARNES, J, OMAR, R, WARRINGTON, E. K, ROSSOR, M. N, WARREN, J. D, FOX, N. C

    Published in Neurology (28-10-2008)
    “…Semantic dementia is a sporadic neurodegenerative disorder characterized by the progressive erosion of semantic processing and is one of the canonical subtypes…”
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    Journal Article
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    Presymptomatic studies in genetic frontotemporal dementia by Rohrer, J.D., Warren, J.D., Fox, N.C., Rossor, M.N.

    Published in Revue neurologique (01-10-2013)
    “…Approximately 20% of patients with the neurodegenerative disorder frontotemporal dementia (FTD) have an autosomal dominant pattern of inheritance. Genetic FTD…”
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    Journal Article Conference Proceeding
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    Primary progressive aphasia: defining genetic and pathological subtypes by Rohrer, J D, Schott, J M

    Published in Current Alzheimer research (01-05-2011)
    “…The primary progressive aphasias (PPA) are a group of clinically, genetically and pathologically heterogeneous neurodegenerative disorders caused by FTLD-tau,…”
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    Journal Article
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    Review: Clinical, genetic and neuroimaging features of frontotemporal dementia by Convery, R., Mead, S., Rohrer, J. D.

    Published in Neuropathology and applied neurobiology (01-02-2019)
    “…Frontotemporal dementia (FTD) is a heterogeneous group of disorders causing neurodegeneration within a network of areas centred on the frontal and temporal…”
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    Journal Article
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    Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation by Alner, K, Hyare, H, Mead, S, Rudge, P, Wroe, S, Rohrer, J D, Ridgway, G R, Ourselin, S, Clarkson, M, Hunt, H, Fox, N C, Webb, T, Collinge, J, Cipolotti, L

    “…BackgroundThe human prion diseases are a group of universally fatal neurodegenerative disorders associated with the auto-catalytic misfolding of the normal…”
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    Journal Article
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    Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review by Seelaar, Harro, Rohrer, Jonathan D, Pijnenburg, Yolande A L, Fox, Nick C, van Swieten, John C

    “…Frontotemporal dementia (FTD) is the second most common young-onset dementia and is clinically characterised by progressive behavioural change, executive…”
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    Journal Article Book Review
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    Automatic classification of MR scans in Alzheimer's disease by Klöppel, Stefan, Stonnington, Cynthia M., Chu, Carlton, Draganski, Bogdan, Scahill, Rachael I., Rohrer, Jonathan D., Fox, Nick C., Jack, Clifford R., Ashburner, John, Frackowiak, Richard S. J.

    Published in Brain (London, England : 1878) (01-03-2008)
    “…To be diagnostically useful, structural MRI must reliably distinguish Alzheimer's disease (AD) from normal aging in individual scans. Recent advances in…”
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    Word-finding difficulty: a clinical analysis of the progressive aphasias by Rohrer, Jonathan D., Knight, William D., Warren, Jane E., Fox, Nick C., Rossor, Martin N., Warren, Jason D.

    Published in Brain (London, England : 1878) (01-01-2008)
    “…The patient with word-finding difficulty presents a common and challenging clinical problem. The complaint of ‘word-finding difficulty’ covers a wide range of…”
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    A data-driven model of brain volume changes in progressive supranuclear palsy by Scotton, W. J., Bocchetta, M., Todd, E., Cash, D. M., Oxtoby, N., VandeVrede, L., Heuer, H., Alexander, D. C., Rowe, J. B., Morris, H. R., Boxer, A., Rohrer, J. D., Wijeratne, P. A.

    Published in Brain communications (2022)
    “…Abstract The most common clinical phenotype of progressive supranuclear palsy is Richardson syndrome, characterized by levodopa unresponsive symmetric…”
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    Journal Article
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