Search Results - "Rohrer, J D"
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Patterns of cortical thinning in the language variants of frontotemporal lobar degeneration
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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2
Classification of primary progressive aphasia and its variants
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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3
The heritability and genetics of frontotemporal lobar degeneration
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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Review: Fluid biomarkers for frontotemporal dementias
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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5
TDP-43 subtypes are associated with distinct atrophy patterns in frontotemporal dementia
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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Measuring disease progression in frontotemporal lobar degeneration: A clinical and MRI study
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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7
Tracking progression in frontotemporal lobar degeneration : Serial MRI in semantic dementia
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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8
Presymptomatic studies in genetic frontotemporal dementia
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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9
Primary progressive aphasia: defining genetic and pathological subtypes
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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Review: Clinical, genetic and neuroimaging features of frontotemporal dementia
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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11
Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation
Published in Journal of neurology, neurosurgery and psychiatry (01-01-2012)“…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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12
Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review
Published in Journal of Neurology, Neurosurgery and Psychiatry (01-05-2011)“…Frontotemporal dementia (FTD) is the second most common young-onset dementia and is clinically characterised by progressive behavioural change, executive…”
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Automatic classification of MR scans in Alzheimer's disease
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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14
A practical approach to diagnosing adult onset leukodystrophies
Published in Journal of neurology, neurosurgery and psychiatry (01-07-2014)Get full text
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15
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration
Published in Brain (London, England : 1878) (01-09-2011)“…Relating clinical symptoms to neuroanatomical profiles of brain damage and ultimately to tissue pathology is a key challenge in the field of neurodegenerative…”
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Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series
Published in Molecular psychiatry (01-12-2020)“…Next-generation genetic sequencing (NGS) technologies facilitate the screening of multiple genes linked to neurodegenerative dementia, but there are few…”
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Corticospinal tract degeneration and temporal lobe atrophy in frontotemporal lobar degeneration TDP‐43 type C pathology
Published in Neuropathology and applied neurobiology (01-04-2020)Get full text
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18
Word-finding difficulty: a clinical analysis of the progressive aphasias
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
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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A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies
Published in Brain (London, England : 1878) (01-09-2011)“…Neuronal intermediate filament inclusion disease and atypical frontotemporal lobar degeneration are rare diseases characterized by ubiquitin-positive…”
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