Yu Tsuyusaki
Yokohama, Japan
Last Updated: 09/26/2026
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Found 28 publications
Efficacy and safety of fenfluramine in Dravet syndrome; A monocentric, observational study focused on initial dose, blood concentration, and reduction of concomitant medications.
Journal: Epilepsy & behavior : E&B
Published: February 14, 2026
Two siblings with acute necrotizing encephalopathy associated with variants of LARS1.
Journal: American journal of medical genetics. Part A
Published: March 16, 2024
Successful treatment with teduglutide for an adolescent with cerebral palsy accompanied by short bowel syndrome.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: February 16, 2024
Role of TOE1 variants at the nuclear localization motif in pontocerebellar hypoplasia 7.
Journal: Journal of human genetics
Published: December 14, 2023
Atypical clinical course in two patients with GNB1 variants who developed acute encephalopathy.
Journal: Brain & development
Published: March 17, 2023
Genetic and clinical features of pediatric-onset hereditary spastic paraplegia: a single-center study in Japan.
Journal: Frontiers in neurology
Published: October 31, 2022
Association between cerebrospinal fluid parameters and developmental and neurological status in glucose transporter 1 deficiency syndrome.
Journal: Journal of the neurological sciences
Published: August 28, 2022
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
Elevation of brain gamma-aminobutyric acid levels is associated with vigabatrin-associated brain abnormalities on magnetic resonance imaging.
Journal: Epilepsy research
Published: November 20, 2021
Last Updated: 09/26/2026