Takeshi Ikeuchi

Niigata, Japan

Last Updated: 09/26/2026

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Found 267 publications

A Novel p. (Leu173del) Mutation in the Presenilin 1 (PSEN1) Gene in Two Sisters with Dominantly Inherited Alzheimer's Disease.

A Novel p. (Leu173del) Mutation in the Presenilin 1 (PSEN1) Gene in Two Sisters with Dominantly Inherited Alzheimer's Disease.

Journal: Internal medicine (Tokyo, Japan)
Published: July 20, 2026

Survey on the involvement of Japanese neurologists in genetic medicine

Survey on the involvement of Japanese neurologists in genetic medicine

Journal: Rinsho shinkeigaku = Clinical neurology
Published: June 17, 2026

Longitudinal associations of serum MCP-1 with cognitive decline and psychological stress in biomarker-confirmed Alzheimer's disease: A pilot study.

Longitudinal associations of serum MCP-1 with cognitive decline and psychological stress in biomarker-confirmed Alzheimer's disease: A pilot study.

Journal: Brain, behavior, & immunity - health
Published: May 28, 2026

Post-mortem diagnosis of CACT deficiency with a novel SLC25A20 variant.

Post-mortem diagnosis of CACT deficiency with a novel SLC25A20 variant.

Journal: Human genome variation
Published: April 27, 2026

Abnormalities in core AD biomarkers precede inflammatory and glial markers in CSF in Autosomal Dominant Alzheimer's Disease.

Abnormalities in core AD biomarkers precede inflammatory and glial markers in CSF in Autosomal Dominant Alzheimer's Disease.

Journal: medRxiv : the preprint server for health sciences
Published: April 10, 2026

Effect of Cognitive Reserve on Age at Symptom Onset and Cognitive Decline in Individuals With Dominantly Inherited Alzheimer Disease.

Effect of Cognitive Reserve on Age at Symptom Onset and Cognitive Decline in Individuals With Dominantly Inherited Alzheimer Disease.

Journal: Neurology
Published: April 08, 2026

A reappraisal of APOE genetic effects on Alzheimer's disease risk in the Japanese population: a meta-analysis.

A reappraisal of APOE genetic effects on Alzheimer's disease risk in the Japanese population: a meta-analysis.

Journal: Molecular neurodegeneration
Published: April 07, 2026

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

Journal: Molecular genetics & genomic medicine
Published: March 23, 2026

Reductions in regional cerebral blood flow and dopamine transporter uptake in a patient with Gerstmann-Sträussler-Scheinker disease harboring the prion protein gene P105L mutation.

Reductions in regional cerebral blood flow and dopamine transporter uptake in a patient with Gerstmann-Sträussler-Scheinker disease harboring the prion protein gene P105L mutation.

Journal: Journal of the neurological sciences
Published: March 16, 2026

Reduced Soluble Ubiquilin2 in Amyotrophic Lateral Sclerosis Carrying Ubiquilin2 (P494L) Mutation: Clinicopathological and Biochemical Evidence From an Autopsy Case.

Reduced Soluble Ubiquilin2 in Amyotrophic Lateral Sclerosis Carrying Ubiquilin2 (P494L) Mutation: Clinicopathological and Biochemical Evidence From an Autopsy Case.

Journal: Neuropathology and applied neurobiology
Published: March 13, 2026

Mass spectrometry-based proteomic profiling of human tauopathy brains suggests mitochondria-associated alterations.

Mass spectrometry-based proteomic profiling of human tauopathy brains suggests mitochondria-associated alterations.

Journal: Frontiers in molecular neuroscience
Published: February 23, 2026

Expansive spatial pattern of Aβ deposition in patients with cerebral amyloid angiopathy: A three-dimensional surface-to-depth analysis.

Expansive spatial pattern of Aβ deposition in patients with cerebral amyloid angiopathy: A three-dimensional surface-to-depth analysis.

Journal: Science advances
Published: February 06, 2026
Showing 1-12 of 267

Last Updated: 09/26/2026