Keitaro Yamada
Kasugai, 4860392, Japan
Last Updated: 09/26/2026
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Found 29 publications
Identifying pathogenic variants in rare pediatric neurological diseases using exome sequencing.
Journal: Scientific reports
Published: June 12, 2024
A Novel Constitutively Active c.98G > C, p.(R33P) Variant in RAB11A Associated with Intellectual Disability Promotes Neuritogenesis and Affects Oligodendroglial Arborization.
Journal: Human mutation
Published: May 17, 2023
Reading impairment after neonatal hypoglycemia with parieto-temporo-occipital injury without cortical blindness: A case report.
Journal: World journal of clinical cases
Published: March 17, 2023
Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 10, 2022
Current status of surviving patients with arginase 1 deficiency in Japan.
Journal: Molecular genetics and metabolism reports
Published: August 26, 2021
Effectiveness of lacosamide in children and young adults previously treated with other sodium channel blockers.
Journal: Epilepsy & behavior : E&B
Published: August 12, 2021
Palaeo-tsunami inundation distances deduced from roundness of gravel particles in tsunami deposits.
Journal: Scientific reports
Published: March 21, 2019
Identification of novel compound heterozygous mutations in ACO2 in a patient with progressive cerebral and cerebellar atrophy.
Journal: Molecular genetics & genomic medicine
Published: September 26, 2018
Last Updated: 09/26/2026