Kenji Watanabe
Kagoshima, Japan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 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
Direct evaluation of neuroaxonal degeneration with the causative genes of neurodegenerative diseases in Drosophila using the automated axon quantification system, MeDUsA.
Journal: Human molecular genetics
Published: August 08, 2022
Efficacy of bezafibrate for preventing myopathic attacks in patients with very long-chain acyl-CoA dehydrogenase deficiency.
Journal: Brain & development
Published: April 01, 2020
Novel AP3B1 compound heterozygous mutations in a Japanese patient with Hermansky-Pudlak syndrome type 2.
Journal: The Journal of dermatology
Published: September 21, 2019
Open-label clinical trial of bezafibrate treatment in patients with fatty acid oxidation disorders in Japan; 2nd report QOL survey.
Journal: Molecular genetics and metabolism reports
Published: July 01, 2019
Two siblings with very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency suffered from rhabdomyolysis after l-carnitine supplementation.
Journal: Molecular genetics and metabolism reports
Published: January 22, 2018
Open-label clinical trial of bezafibrate treatment in patients with fatty acid oxidation disorders in Japan.
Journal: Molecular genetics and metabolism reports
Published: December 22, 2017
Manifestations and characteristics of congenital adrenal hyperplasia-associated encephalopathy.
Journal: Brain & development
Published: December 07, 2015
Showing 1-8 of 8
Last Updated: 09/26/2026