Ayako Umemura
Nagoya, Japan
Last Updated: 09/26/2026
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Found 8 publications
Redox control in arsenic accumulation with organic matter derived from a varved lacustrine deposit in the Jurassic accretionary complexes.
Journal: Journal of hazardous materials
Published: September 04, 2024
A 12-kb structural variation in progressive myoclonic epilepsy was newly identified by long-read whole-genome sequencing.
Journal: Journal of human genetics
Published: December 07, 2018
Clinical and genetic diversities of Charcot-Marie-Tooth disease with MFN2 mutations in a large case study.
Journal: Journal of the peripheral nervous system : JPNS
Published: April 30, 2017
Two pediatric cases of chronic progressive subdural hematoma with brain atrophy following acute encephalitis/encephalopathy requiring surgical hematoma removal
Journal: No to hattatsu = Brain and development
Published: March 26, 2016
Arts syndrome with a novel missense mutation in the PRPS1 gene: A case report.
Journal: Brain & development
Published: March 29, 2015
Thalamic lesions in acute encephalopathy with biphasic seizures and late reduced diffusion.
Journal: Pediatric neurology
Published: May 18, 2014
SLC16A2 mutations in two Japanese patients with Allan-Herndon-Dudley syndrome.
Journal: Human genome variation
Published: January 01, 2014
Showing 1-8 of 8
Last Updated: 09/26/2026