Mai Tanaka
Tsukuba, Japan
Last Updated: 09/26/2026
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Found 15 publications
Adeno-Associated Virus Gene Therapy for Spinal Muscular Atrophy Induces Hepatotoxicity via Cytokine and Macrophage Activation.
Journal: Liver international : official journal of the International Association for the Study of the Liver
Published: October 27, 2025
A boy with autism spectrum disorder with antibodies to the NMDA-type glutamate receptor: nine-year follow-up, changes in cognitive function .
Journal: Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence
Published: April 22, 2025
Valproate and lamotrigine combination therapy in children with drug-resistant focal epilepsy: an observational analysis focusing on neuroimaging abnormalities.
Journal: Brain & development
Published: April 04, 2025
A Case of Anorexia Nervosa with Focal Cortical Dysplasia.
Journal: Case reports in psychiatry
Published: December 09, 2023
Identification of a novel splice-site WWOX variant with paternal uniparental isodisomy in a patient with infantile epileptic encephalopathy.
Journal: American journal of medical genetics. Part A
Published: November 14, 2023
A male with ganglioneuroblastoma cerebrospinal hemorrhages, cardiomyopathy, and retinopathy due to severe hypertension.
Journal: Pediatric blood & cancer
Published: February 06, 2023
Boys with attention-deficit/hyperactivity disorder perform wider and fewer finger tapping than typically developing boys - Peer comparisons and the effects of methylphenidate from an exploratory perspective.
Journal: Brain & development
Published: July 24, 2021
Novel ACOX1 mutations in two siblings with peroxisomal acyl-CoA oxidase deficiency.
Journal: Brain & development
Published: June 12, 2020
Variants in KIF2A cause broad clinical presentation; the computational structural analysis of a novel variant in a patient with a cortical dysplasia, complex, with other brain malformations 3.
Journal: American journal of medical genetics. Part A
Published: February 11, 2020
Novel ARX mutation identified in infantile spasm syndrome patient.
Journal: Human genome variation
Published: January 19, 2020
Quantitative assessment of fine motor skills in children using magnetic sensors.
Journal: Brain & development
Published: November 12, 2019
A case of autism spectrum disorder with cleft lip and palate carrying a mutation in exon 8 of AUTS2.
A case of autism spectrum disorder with cleft lip and palate carrying a mutation in exon 8 of AUTS2.
Journal: Clinical case reports
Published: March 21, 2019
Last Updated: 09/26/2026