Yoshihiro Toda
Tokushima, Japan
Last Updated: 09/26/2026
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Found 20 publications
A female case of L1 syndrome that may have developed due to skewed X inactivation.
Journal: Brain & development
Published: February 01, 2024
A case of epilepsy with myoclonic atonic seizures caused by SLC6A1 gene mutation due to balanced chromosomal translocation.
Journal: Brain & development
Published: December 22, 2022
Molecular diagnosis of an infant with TSC2/PKD1 contiguous gene syndrome.
Journal: Human genome variation
Published: May 08, 2020
Survey of patients with spinal muscular atrophy on the island of Shikoku, Japan.
Journal: Brain & development
Published: November 12, 2019
Improvement of epilepsy with lacosamide in a patient with ring chromosome 20 syndrome.
Journal: Brain & development
Published: August 22, 2019
Multi-delay arterial spin labeling brain magnetic resonance imaging study for pediatric autism.
Journal: Brain & development
Published: June 20, 2019
A 16q22.2-q23.1 deletion identified in a male infant with West syndrome.
Journal: Brain & development
Published: April 16, 2019
Prominent T-wave and ST-segment elevation on electrocardiogram during neonatal seizure.
Journal: Pediatrics and neonatology
Published: January 26, 2018
A rare male patient with classic Rett syndrome caused by MeCP2_e1 mutation.
Journal: American journal of medical genetics. Part A
Published: May 28, 2017
A Proton Magnetic Resonance Spectroscopic Study in Autism Spectrum Disorder Using a 3-Tesla Clinical Magnetic Resonance Imaging (MRI) System: The Anterior Cingulate Cortex and the Left Cerebellum.
Journal: Journal of child neurology
Published: April 20, 2017
Assessment of Anterior Cingulate Cortex (ACC) and Left Cerebellar Metabolism in Asperger's Syndrome with Proton Magnetic Resonance Spectroscopy (MRS).
Journal: PloS one
Published: June 15, 2016
Detailed analysis of 26 cases of 1q partial duplication/triplication syndrome.
Journal: American journal of medical genetics. Part A
Published: April 06, 2015
Last Updated: 09/26/2026