Yuko Ichimiya
Fukuoka, Japan
Last Updated: 09/26/2026
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Found 30 publications
Persistent lymphopenia in a Japanese boy with neuronal ceroid lipofuscinosis type 3.
Journal: European journal of medical genetics
Published: September 05, 2025
Glutamate in cerebrospinal fluid as a diagnostic marker for acute encephalopathy in childhood.
Journal: Brain & development
Published: March 16, 2025
Persistent intracranial hyper-inflammation in ruptured cerebral aneurysm after COVID-19: case report and review of the literature.
Journal: BMC neurology
Published: July 12, 2023
Progressive myoclonic epilepsy as an expanding phenotype of NGLY1-associated congenital deglycosylation disorder: A case report and review of the literature.
Journal: European journal of medical genetics
Published: July 03, 2023
Heterogeneity and mitochondrial vulnerability configurate the divergent immunoreactivity of human induced microglia-like cells.
Journal: Clinical immunology (Orlando, Fla.)
Published: June 01, 2023
Long-lasting pain and somatosensory disturbances in children with myelin oligodendrocyte glycoprotein antibody-associated disease.
Journal: European journal of pediatrics
Published: January 05, 2023
Divergent neurodevelopmental profiles of very-low-birth-weight infants.
Journal: Pediatric research
Published: December 27, 2022
Paradoxical spells during ACTH treatment in an infant with Tetralogy of Fallot.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: December 22, 2022
Critical vitamin deficiencies in autism spectrum disorder: Reversible and irreversible outcomes.
Journal: European journal of clinical nutrition
Published: April 04, 2022
Acute-phase electroencephalography for an infantile atypical teratoid/rhabdoid tumor.
Journal: Clinical neurology and neurosurgery
Published: June 12, 2021
BCS1L mutations produce Fanconi syndrome with developmental disability.
Journal: Journal of human genetics
Published: April 04, 2021
Last Updated: 09/26/2026