Ruoyi Ishikawa

Hiroshima, Japan

Last Updated: 09/26/2026

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Found 8 publications

A novel conditional knock-in mouse model for APOE4-to-APOE3 switching.

A novel conditional knock-in mouse model for APOE4-to-APOE3 switching.

Journal: Neurobiology of disease

Published: June 06, 2025

A Case of Anti-N-Methyl-D-Aspartate Receptor (NMDAR) Encephalitis With Video-Documented Psychogenic Nonepileptic Seizures (PNES)-Mimicking Episodes Initially Considered as Somatic Symptom Disorder.

A Case of Anti-N-Methyl-D-Aspartate Receptor (NMDAR) Encephalitis With Video-Documented Psychogenic Nonepileptic Seizures (PNES)-Mimicking Episodes Initially Considered as Somatic Symptom Disorder.

Journal: Cureus

Published: February 20, 2025

Presenteeism in people with previous and current epilepsy: Determinants and psychosocial associations.

Presenteeism in people with previous and current epilepsy: Determinants and psychosocial associations.

Journal: Seizure

Published: October 21, 2024

Antibody-recognizing residues 188-211 of TMEM106B exhibit immunohistochemical reactivity with the TMEM106B C-terminal fragment.

Antibody-recognizing residues 188-211 of TMEM106B exhibit immunohistochemical reactivity with the TMEM106B C-terminal fragment.

Journal: Frontiers in neuroscience

Published: June 30, 2023

Swallowing sound evaluation using an electronic stethoscope and artificial intelligence analysis for patients with amyotrophic lateral sclerosis.

Swallowing sound evaluation using an electronic stethoscope and artificial intelligence analysis for patients with amyotrophic lateral sclerosis.

Journal: Frontiers in neurology

Published: April 25, 2023

Case report: Mitochondrial trifunctional protein deficiency caused by HADHB gene mutation (c.1175C>T) characterized by higher brain dysfunction followed by neuropathy, presented gadolinium enhancement on brain imaging in an adult patient.

Case report: Mitochondrial trifunctional protein deficiency caused by HADHB gene mutation (c.1175C>T) characterized by higher brain dysfunction followed by neuropathy, presented gadolinium enhancement on brain imaging in an adult patient.

Journal: Frontiers in neurology

Published: March 16, 2023

A 36-year-old Man with Repeated Short-term Transient Hyperammonemia and Impaired Consciousness with a Confirmed Carbamoyl Phosphate Synthase 1 Gene Monoallelic Mutation.

A 36-year-old Man with Repeated Short-term Transient Hyperammonemia and Impaired Consciousness with a Confirmed Carbamoyl Phosphate Synthase 1 Gene Monoallelic Mutation.

Journal: Internal medicine (Tokyo, Japan)

Published: October 21, 2021

Initial deterioration and intravenous methylprednisolone therapy in patients with myasthenia gravis.

Initial deterioration and intravenous methylprednisolone therapy in patients with myasthenia gravis.

Journal: Journal of the neurological sciences

Published: September 16, 2019

Showing 1-8 of 8

Last Updated: 09/26/2026