Hiroaki Yaguchi
Japan
Last Updated: 09/26/2026
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Found 76 publications
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
Association between the peptide spectrum match values of LGI1, ADAM22, ADAM23 and DLG4 in the immunoprecipitation products of five autoimmune encephalitis cases with LGI1 antibody: A case series.
Journal: Internal medicine (Tokyo, Japan)
Published: June 17, 2026
Episodic ataxia type 2 with a novel CACNA1A variant: A video case report.
Journal: Clinical neurology and neurosurgery
Published: March 29, 2026
Continuing decline of multisystemic subtypes and increasing unidentified cases in autosomal dominant spinocerebellar ataxia under health insurance coverage in Hokkaido.
Journal: Journal of the neurological sciences
Published: March 20, 2026
Nationwide screening identifies an expanded clinical spectrum of anti-KLHL11 antibody-associated neurologic disease in Japan.
Journal: Journal of neurology
Published: March 12, 2026
Prevalence and profiles of clinically diagnosed autoimmune cerebellar ataxia in a Japanese nationwide survey.
Journal: Journal of neurology
Published: January 06, 2026
Haplotype analysis of spinocerebellar ataxia type 36 suggests a shared permissive core haplotype across populations.
Journal: Journal of human genetics
Published: December 04, 2025
A Retrospective Study of 116 Multiple Sclerosis Patients with Dimethyl Fumarate Treatment in a Single Institution in Japan.
Journal: Internal medicine (Tokyo, Japan)
Published: November 26, 2025
Contrasting Outcomes in Two Cases of Anti-contactin-associated Protein-like 2 Autoimmune Encephalitis.
Journal: Internal medicine (Tokyo, Japan)
Published: November 12, 2025
Limited-Stage Small-Cell Lung Cancer With Severe Paraneoplastic Limbic Encephalitis Successfully Treated With Chemoradiotherapy Followed by Immune Checkpoint Inhibitor Maintenance Therapy: A Case Report.
Journal: Clinical lung cancer
Published: October 12, 2025
Leukoencephalopathy with primary familial brain calcification: A rare phenotype associated with a novel SLC20A2 frameshift.
Journal: Clinical neurology and neurosurgery
Published: September 07, 2025
Trends in Invasive Interventions and Risk Factors for Early Critical Events in Multiple System Atrophy.
Journal: Cerebellum (London, England)
Published: May 18, 2025
Last Updated: 09/26/2026