Takashi Haraguchi

Okayama, Japan

Last Updated: 09/26/2026

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Found 13 publications

Correction: Cerebral Braak stage and amygdala granular fuzzy astrocyte status have independent effects on neuronal 3R-tau and 4R-tau accumulations in the olfactory bulb, respectively, in cases with low to intermediate AD neuropathologic change.

Correction: Cerebral Braak stage and amygdala granular fuzzy astrocyte status have independent effects on neuronal 3R-tau and 4R-tau accumulations in the olfactory bulb, respectively, in cases with low to intermediate AD neuropathologic change.

Journal: Acta neuropathologica

Published: July 27, 2025

Biallelic variants in DNAJC7 cause familial amyotrophic lateral sclerosis with the TDP-43 pathology.

Biallelic variants in DNAJC7 cause familial amyotrophic lateral sclerosis with the TDP-43 pathology.

Journal: Acta neuropathologica

Published: January 23, 2025

Cerebral Braak stage and amygdala granular fuzzy astrocyte status have independent effects on neuronal 3R-tau and 4R-tau accumulations in the olfactory bulb, respectively, in cases with low to intermediate AD neuropathologic change.

Cerebral Braak stage and amygdala granular fuzzy astrocyte status have independent effects on neuronal 3R-tau and 4R-tau accumulations in the olfactory bulb, respectively, in cases with low to intermediate AD neuropathologic change.

Journal: Acta neuropathologica

Published: January 19, 2025

Pure argyrophilic grain disease revisited: independent effects on limbic, neocortical, and striato-pallido-nigral degeneration and the development of dementia in a series with a low to moderate Braak stage.

Pure argyrophilic grain disease revisited: independent effects on limbic, neocortical, and striato-pallido-nigral degeneration and the development of dementia in a series with a low to moderate Braak stage.

Journal: Acta neuropathologica communications

Published: June 15, 2024

Amygdala granular fuzzy astrocytes are independently associated with both LATE neuropathologic change and argyrophilic grains: a study of Japanese series with a low to moderate Braak stage.

Amygdala granular fuzzy astrocytes are independently associated with both LATE neuropathologic change and argyrophilic grains: a study of Japanese series with a low to moderate Braak stage.

Journal: Acta neuropathologica communications

Published: August 21, 2023

Amygdala granular fuzzy astrocytes as lesions preceding development of argyrophilic grains: data from 239 autopsy cases.

Amygdala granular fuzzy astrocytes as lesions preceding development of argyrophilic grains: data from 239 autopsy cases.

Journal: Free neuropathology

Published: June 15, 2022

Four-repeat tauopathies and late-onset psychiatric disorders: Etiological relevance or incidental findings?

Four-repeat tauopathies and late-onset psychiatric disorders: Etiological relevance or incidental findings?

Journal: Neuropathology : official journal of the Japanese Society of Neuropathology

Published: February 20, 2022

Factors associated with development and distribution of granular/fuzzy astrocytes in neurodegenerative diseases.

Factors associated with development and distribution of granular/fuzzy astrocytes in neurodegenerative diseases.

Journal: Brain pathology (Zurich, Switzerland)

Published: October 23, 2019

Young adult-onset, very slowly progressive cognitive decline with spastic paraparesis in Alzheimer's disease with cotton wool plaques due to a novel presenilin1 G417S mutation.

Young adult-onset, very slowly progressive cognitive decline with spastic paraparesis in Alzheimer's disease with cotton wool plaques due to a novel presenilin1 G417S mutation.

Journal: Acta neuropathologica communications

Published: January 03, 2019

A novel presenilin 1 mutation (Leu418Trp) associated with spasticity, parkinsonism, and white matter lesion in a dominant Alzheimer's family.

A novel presenilin 1 mutation (Leu418Trp) associated with spasticity, parkinsonism, and white matter lesion in a dominant Alzheimer's family.

Journal: Journal of the neurological sciences

Published: November 29, 2017

Frontotemporal lobar degeneration due to P301L tau mutation showing apathy and severe frontal atrophy but lacking other behavioral changes: A case report and literature review.

Frontotemporal lobar degeneration due to P301L tau mutation showing apathy and severe frontal atrophy but lacking other behavioral changes: A case report and literature review.

Journal: Neuropathology : official journal of the Japanese Society of Neuropathology

Published: July 16, 2017

Neuropathological comorbidity associated with argyrophilic grain disease.

Neuropathological comorbidity associated with argyrophilic grain disease.

Journal: Neuropathology : official journal of the Japanese Society of Neuropathology

Published: June 26, 2017

Showing 1-12 of 13

Last Updated: 09/26/2026