Akihiko Miyauchi
Tochigi, Japan
Last Updated: 09/26/2026
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Found 27 publications
Ferroptosis susceptibility in primary coenzyme Q10 deficiency: Cellular insights from patient fibroblasts and clinical course of six individuals.
Journal: Brain & development
Published: July 16, 2025
Synthetic aporphine alkaloids are potential therapeutics for Leigh syndrome.
Journal: Scientific reports
Published: January 09, 2024
Apomorphine is a potent inhibitor of ferroptosis independent of dopaminergic receptors.
Journal: Scientific reports
Published: September 16, 2023
Biallelic null variants in PNPLA8 cause microcephaly by reducing the number of basal radial glia.
Journal: Brain : a journal of neurology
Published: May 18, 2023
Biallelic structural variations within FGF12 detected by long-read sequencing in epilepsy.
Journal: Life science alliance
Published: March 06, 2023
Total and reduced/oxidized forms of coenzyme Q10 in fibroblasts of patients with mitochondrial disease.
Journal: Molecular genetics and metabolism reports
Published: October 25, 2022
A Case of Infantile Mitochondrial Cardiomyopathy Treated with a Combination of Low-Dose Propranolol and Cibenzoline for Left Ventricular Outflow Tract Stenosis.
Journal: International heart journal
Published: September 14, 2022
Low donor chimerism may be sufficient to prevent demyelination in adrenoleukodystrophy.
Journal: JIMD reports
Published: August 19, 2021
Two cases of DYNC1H1 mutations with intractable epilepsy.
Journal: Brain & development
Published: December 23, 2020
MOG-Ab titer-guided approach for steroid tapering to prevent relapse in children with mog antibody-associated adem diseases: A case report.
Journal: Multiple sclerosis and related disorders
Published: May 09, 2020
De Novo Truncating Variants in the Last Exon of SEMA6B Cause Progressive Myoclonic Epilepsy.
Journal: American journal of human genetics
Published: November 20, 2019
Last Updated: 09/26/2026