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Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementiaFrequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyFrontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological featuresNeologistic jargon aphasia and agraphia in primary progressive aphasiaWord-finding difficulty: a clinical analysis of the progressive aphasias.Neuronal network disintegration: common pathways linking neurodegenerative diseasesThe language profile of posterior cortical atrophyProgressive Supranuclear Palsy and Corticobasal Degeneration: Pathophysiology and Treatment OptionsUsing exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvementThe habenula: an under-recognised area of importance in frontotemporal dementia?Craving for music after treatment for partial epilepsy.Auditory hedonic phenotypes in dementia: A behavioural and neuroanatomical analysis.A physiological signature of sound meaning in dementia.Delayed auditory feedback simulates features of nonfluent primary progressive aphasiaCommon variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.Receptive prosody in nonfluent primary progressive aphasias.Mapping the progression of progranulin-associated frontotemporal lobar degenerationNon-verbal sound processing in the primary progressive aphasias.Abnormal laughter-like vocalisations replacing speech in primary progressive aphasia.Genetic and clinical features of progranulin-associated frontotemporal lobar degenerationLongitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansions.Imaging endpoints for clinical trials in Alzheimer's disease.Redefining the phenotype of ALSP and AARS2 mutation-related leukodystrophyCompulsive versifying after treatment of transient epileptic amnesia.Perry syndrome due to the DCTN1 G71R mutation: a distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure.White matter hyperintensities are seen only in GRN mutation carriers in the GENFI cohort.Measuring disease progression in frontotemporal lobar degeneration: a clinical and MRI study.Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review.Cognitive reserve and TMEM106B genotype modulate brain damage in presymptomatic frontotemporal dementia: a GENFI study.Apraxia in progressive nonfluent aphasia.FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration.Frontotemporal dementia and its subtypes: a genome-wide association study.Phenomenology and anatomy of abnormal behaviours in primary progressive aphasiaStructural neuroanatomy of tinnitus and hyperacusis in semantic dementia.Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration.Altered body schema processing in frontotemporal dementia with C9ORF72 mutations.Syndromes of nonfluent primary progressive aphasia: a clinical and neurolinguistic analysis.Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutationsProgressive logopenic/phonological aphasia: erosion of the language network.Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R gene.
P50
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P50
description
hulumtues
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researcher
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wetenschapper
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հետազոտող
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name
Jonathan D Rohrer
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Jonathan D Rohrer
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Jonathan D Rohrer
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Jonathan D Rohrer
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Jonathan D Rohrer
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type
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Jonathan D Rohrer
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Jonathan D Rohrer
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Jonathan D Rohrer
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Jonathan D Rohrer
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Jonathan D Rohrer
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Jonathan Rohrer
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Jonathan D Rohrer
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Jonathan D Rohrer
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Jonathan D Rohrer
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Jonathan D Rohrer
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Jonathan D Rohrer
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P106
P21
P31
P496
0000-0002-6155-8417