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Koji Kasanuki

Researcher at Mayo Clinic

Publications -  64
Citations -  1169

Koji Kasanuki is an academic researcher from Mayo Clinic. The author has contributed to research in topics: Dementia with Lewy bodies & Dementia. The author has an hindex of 17, co-authored 59 publications receiving 883 citations. Previous affiliations of Koji Kasanuki include Juntendo University & University of Alabama at Birmingham.

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CSF1R-related leukoencephalopathy: A major player in primary microgliopathies

TL;DR: The current knowledge of CSF1R-related leukoencephalopathy is addressed and the putative pathophysiology is discussed, with a focus on microglia, as well as future research directions.
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Dementia with Lewy bodies: early diagnostic challenges.

TL;DR: A conceptual framework is proposed to identify these symptomatic but non‐demented individuals that led to suspect the underlying pathophysiology of Lewy body disease and further prospective study is warranted to determine the clinical significance of LB‐related symptoms in non‐Demented patients.
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Retrospective survey of prodromal symptoms in dementia with Lewy bodies: comparison with Alzheimer's disease.

TL;DR: Paying attention to non-motor symptoms of PD may help DLB diagnosis in the early stage, especially in terms of its differentiation from AD.
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Distribution of cerebral amyloid deposition and its relevance to clinical phenotype in Lewy body dementia.

TL;DR: It is suggested that amyloid deposition may contribute to the timing of the onset of dementia relative to that of parkinsonism in Lewy body dementia.
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Localization of MAP1-LC3 in vulnerable neurons and Lewy bodies in brains of patients with dementia with Lewy bodies.

TL;DR: Investigation of potential neuropathologic and biochemical alterations of autophagy-lysosome pathway-related proteins in the brains of patients with dementia with Lewy bodies, Alzheimer disease, and control subjects using antibodies against Ras-related protein Rab-7B finds specific accumulation of the autophagosomal LC3-II isoform in detergent-insoluble fractions from DLB brains.