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An update on semantic dementia: genetics, imaging, and pathologyRetrosplenial cortex (BA 29) volumes in behavioral variant frontotemporal dementia and Alzheimer's diseaseAlport retinopathy results from "severe" COL4A5 mutations and predicts early renal failure.Classification of FTLD-TDP cases into pathological subtypes using antibodies against phosphorylated and non-phosphorylated TDP43.Assessment of amyloid β in pathologically confirmed frontotemporal dementia syndromes.Cerebellar integrity in the amyotrophic lateral sclerosis-frontotemporal dementia continuumThe use of ocular abnormalities to diagnose X-linked Alport syndrome in children.Terra incognita-cerebellar contributions to neuropsychiatric and cognitive dysfunction in behavioral variant frontotemporal dementia.Spread of pathology in amyotrophic lateral sclerosis: assessment of phosphorylated TDP-43 along axonal pathways.Cerebellar atrophy in neurodegeneration-a meta-analysis.The pathogenesis of cingulate atrophy in behavioral variant frontotemporal dementia and Alzheimer's disease.Beyond the temporal pole: limbic memory circuit in the semantic variant of primary progressive aphasia.New criteria for frontotemporal dementia syndromes: clinical and pathological diagnostic implications.TDP-43 in the hypoglossal nucleus identifies amyotrophic lateral sclerosis in behavioral variant frontotemporal dementia.ALS/FTLD: experimental models and reality.The retinal "lozenge" or "dull macular reflex" in Alport syndrome may be associated with a severe retinopathy and early-onset renal failure.The Chemical Chaperone, PBA, Reduces ER Stress and Autophagy and Increases Collagen IV α5 Expression in Cultured Fibroblasts From Men With X-Linked Alport Syndrome and Missense Mutations.Multiple neuronal pathologies are common in young patients with pathologically proven Frontotemporal lobar degeneration.In vivo and post-mortem memory circuit integrity in frontotemporal dementia and Alzheimer's disease.Network-selective vulnerability of the human cerebellum to Alzheimer's disease and frontotemporal dementia.von Economo Neuron Density and Thalamus Volumes in Behavioral Deficits in Frontotemporal Dementia Cases with and without a C9ORF72 Repeat Expansion.Cerebellar neuronal loss in amyotrophic lateral sclerosis cases with ATXN2 intermediate repeat expansions.TDP-43 proteinopathies: pathological identification of brain regions differentiating clinical phenotypes.Frontotemporal dementia associated with the C9ORF72 mutation: a unique clinical profile
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description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Rachel Tan
@ast
Rachel Tan
@en
Rachel Tan
@es
Rachel Tan
@nl
Rachel Tan
@sl
type
label
Rachel Tan
@ast
Rachel Tan
@en
Rachel Tan
@es
Rachel Tan
@nl
Rachel Tan
@sl
prefLabel
Rachel Tan
@ast
Rachel Tan
@en
Rachel Tan
@es
Rachel Tan
@nl
Rachel Tan
@sl
P106
P21
P31
P496
0000-0002-0385-4090
P569
2000-01-01T00:00:00Z