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Employment (2)

National Hospital Organization, Omuta National Hospital: Omuta, JP

2023-04-01 to present | Director (Neuropathology Center)
Employment
Source: Self-asserted source
Hiroyuki Honda

Kyushu University: Fukuoka, JP

2021-04-01 to 2023-03-31 | Associate Professor (Neuropathology)
Employment
Source: Self-asserted source
Hiroyuki Honda

Works (20)

Accumulation Area of a Japanese PRNP P102L Variant Associated With Gerstmann-Sträussler-Scheinker Disease: The Ariake PRNP P102L Variant

Journal of Clinical Neurology
2024 | Journal article
Contributors: Kohei Suzuyama; Makoto Eriguchi; Hiromu Minagawa; Hiroyuki Honda; Keita Kai; Tetsuyuki Kitamoto; Hideo Hara
Source: check_circle
Crossref

Dopaminergic neurodegeneration in Gerstmann-Sträussler-Scheinker (P102L) disease: insights from imaging and pathological examination.

2024 | Journal article
Contributors: Hiroyuki Honda
Source: Self-asserted source
Hiroyuki Honda

Novel method for classification of prion diseases by detecting PrPres signal patterns from formalin-fixed paraffin-embedded samples

2024 | Journal article
Contributors: Hiroyuki Honda
Source: Self-asserted source
Hiroyuki Honda

Association between hypothalamic Alzheimer's disease pathology and body mass index: The Hisayama study

Neuropathology
2024-10 | Journal article
Contributors: Kaoru Yagita; Hiroyuki Honda; Tomoyuki Ohara; Sachiko Koyama; Hideko Noguchi; Yoshinao Oda; Ryo Yamasaki; Noriko Isobe; Toshiharu Ninomiya
Source: check_circle
Crossref

Altered expression of human myxovirus resistance protein A in amyotrophic lateral sclerosis

Journal of Neuropathology & Experimental Neurology
2024-09-01 | Journal article
Contributors: Hiroyuki Honda; Shoko Sadashima; Motoi Yoshimura; Naonori Sakurada; Sachiko Koyama; Kaoru Yagita; Hideomi Hamasaki; Hideko Noguchi; Hajime Arahata; Naokazu Sasagasako
Source: check_circle
Crossref

Increased expression of human antiviral protein MxA in FUS proteinopathy in amyotrophic lateral sclerosis

Brain Pathology
2024-03 | Journal article
Contributors: Hiroyuki Honda; Kaoru Yagita; Hajime Arahata; Hideomi Hamasaki; Hideko Noguchi; Sachiko Koyama; Naokazu Sasagasako
Source: check_circle
Crossref

Ribosomal protein SA is a common component of neuronal intranuclear inclusions in polyglutamine diseases and Marinesco bodies

Neuropathology
2024-02 | Journal article
Contributors: Kaoru Yagita; Shoko Sadashima; Sachiko Koyama; Hideko Noguchi; Hideomi Hamasaki; Naokazu Sasagasako; Hiroyuki Honda
Source: check_circle
Crossref

Altered properties of amyloidogenic prion protein in genetic Creutzfeldt-Jakob disease with PRNP V180I mutation in response to pentosan polysulfate

2023 | Journal article
Contributors: Hiroyuki Honda
Source: Self-asserted source
Hiroyuki Honda

Mutated FUS in familial amyotrophic lateral sclerosis involves multiple hnRNPs in the formation of neuronal cytoplasmic inclusions

Journal of Neuropathology & Experimental Neurology
2023-02-21 | Journal article
Contributors: Hiroyuki Honda; Motoi Yoshimura; Hajime Arahata; Kaoru Yagita; Shoko Sadashima; Hideomi Hamasaki; Masahiro Shijo; Sachiko Koyama; Hideko Noguchi; Naokazu Sasagasako
Source: check_circle
Crossref

A Comparative Study of Site-Specific Distribution of Aging-Related Tau Astrogliopathy and Its Risk Factors Between Alzheimer Disease and Cognitive Healthy Brains: The Hisayama Study

Journal of neuropathology and experimental neurology
2022 | Journal article
Part of ISSN: 0022-3069
Source: Self-asserted source
Hiroyuki Honda
grade
Preferred source (of 2)‎

Amyotrophic lateral sclerosis with TDP-43 abnormalities exhibiting globular glial tau inclusions in frontotemporal lobes and pallido-nigral system

Neuropathology : official journal of the Japanese Society of Neuropathology
2022 | Journal article
Part of ISSN: 0919-6544
Source: Self-asserted source
Hiroyuki Honda
grade
Preferred source (of 3)‎

Characteristic distribution and molecular properties of normal cellular prion protein in human endocrine and exocrine tissues

Scientific reports
2022 | Journal article
Part of ISSN: 2045-2322
Source: Self-asserted source
Hiroyuki Honda
grade
Preferred source (of 2)‎

Chronological Changes in the Expression Pattern of Hippocampal Prion Proteins During Disease Progression in Sporadic Creutzfeldt-Jakob Disease MM1 Subtype

Journal of neuropathology and experimental neurology
2022 | Journal article
Part of ISSN: 0022-3069
Source: Self-asserted source
Hiroyuki Honda
grade
Preferred source (of 2)‎

Silence of resident microglia in GPI anchorless prion disease and activation of microglia in Gerstmann-Sträussler-Scheinker disease and sporadic Creutzfeldt-Jakob disease.

Journal of neuropathology and experimental neurology
2022-12 | Journal article
Contributors: Noguchi H; Koyama S; Yagita K; Shijo M; Matsuzono K; Hamasaki H; Kanemaru T; Okamoto T; Kai K; Aishima S et al.
Source: Self-asserted source
Hiroyuki Honda via Europe PubMed Central

Optic nerve atrophy and visual disturbance following PRNP Y162X truncation mutation

Journal of the neurological sciences
2021 | Journal article
Part of ISSN: 0022-510X
Source: Self-asserted source
Hiroyuki Honda
grade
Preferred source (of 2)‎

Prion Gene PRNP Y162X Truncation Mutation Can Induce a Refractory Esophageal Achalasia

Tauopathy in basal ganglia involvement is exacerbated in a subset of patients with Alzheimer's disease: The Hisayama study

Alzheimer's & dementia (Amsterdam, Netherlands)
2019 | Journal article
Part of ISSN: 2352-8729
Source: Self-asserted source
Hiroyuki Honda
grade
Preferred source (of 2)‎

Four-repeat tau dominant pathology in a congenital myotonic dystrophy type 1 patient with mental retardation

Brain pathology (Zurich, Switzerland)
2018 | Journal article
Part of ISSN: 1015-6305
Source: Self-asserted source
Hiroyuki Honda
grade
Preferred source (of 2)‎

Recent Increases in Hippocampal Tau Pathology in the Aging Japanese Population: The Hisayama Study

Journal of Alzheimer's disease : JAD
2017 | Journal article
Part of ISSN: 1387-2877
Source: Self-asserted source
Hiroyuki Honda
grade
Preferred source (of 2)‎

C-Terminal-Deleted Prion Protein Fragment Is a Major Accumulated Component of Systemic PrP Deposits in Hereditary Prion Disease With a 2-Bp (CT) Deletion in PRNP Codon 178

Journal of neuropathology and experimental neurology
2016 | Journal article
Part of ISSN: 0022-3069
Source: Self-asserted source
Hiroyuki Honda
grade
Preferred source (of 2)‎

Peer review (2 reviews for 2 publications/grants)

Review activity for Acta neuropathologica communications. (1)
Review activity for Journal of neurology, neurosurgery and psychiatry (1)