Kiyohiro Kim
Amagasaki, Japan
Last Updated: 09/26/2026
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Found 13 publications
Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.
Journal: Journal of human genetics
Published: April 04, 2026
Infantile epileptic spasms syndrome secondary to diffuse low-grade glioma, MAPK pathway-altered: The importance of early surgical intervention.
Journal: Epileptic disorders : international epilepsy journal with videotape
Published: March 18, 2026
A simple and reliable electroencephalogram montage for detecting and managing electrographic seizures in children with acute encephalitis and encephalopathy.
Journal: Epilepsy research
Published: March 14, 2025
Genome sequencing provides high diagnostic yield and new etiological insights for intellectual disability and developmental delay.
Journal: NPJ genomic medicine
Published: March 11, 2025
Preliminary report for Epilepsia Open A case of West syndrome with severe global developmental delay and confirmed KIF5A gene variant.
Journal: Epilepsia open
Published: April 25, 2020
An unusual manifestation of Sjögren syndrome encephalitis.
Journal: Brain & development
Published: February 06, 2018
Intraoperative cortico-cortical evoked potentials show disconnection of the motor cortex from the epileptogenic network during subtotal hemispherotomy.
Journal: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
Published: October 24, 2017
A child with acute transverse myelitis requiring permanent pacemaker implantation.
Journal: Brain & development
Published: February 01, 2017
Reply to the remarks about "A pediatric patient of hemorrhagic acute transverse myelitis".
Journal: Brain & development
Published: December 27, 2016
Quinidine therapy for West syndrome with KCNTI mutation: A case report.
Journal: Brain & development
Published: May 26, 2016
Last Updated: 09/26/2026