Sawako Furukawa
Nagoya, 4648601, Japan
Last Updated: 09/26/2026
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Found 10 publications
Compound heterozygous CHAT gene mutations, a missense and a splice site variant, in two siblings with congenital myasthenic syndrome.
Journal: Scientific reports
Published: June 03, 2025
Genomic architecture of bipolar disorder in Japan: Insights from genomic structural equation modeling.
Journal: Psychiatry and clinical neurosciences
Published: May 24, 2025
Whole-genome sequencing analysis of Japanese autism spectrum disorder trios.
Journal: Psychiatry and clinical neurosciences
Published: September 05, 2024
Treatment-resistant schizophrenia with 22q11.2 deletion and additional genetic defects.
Journal: Neuropsychopharmacology reports
Published: June 14, 2024
Correction to: RFC1‑related disorder presenting recurrent syncope.
Journal: Journal of neurology
Published: May 27, 2024
RFC1-related disorder presenting recurrent syncope.
Journal: Journal of neurology
Published: November 11, 2023
Case reports of two siblings with autism spectrum disorder and 15q13.3 deletions.
Journal: Neuropsychopharmacology reports
Published: December 26, 2022
Concerns and needs of people with intellectual disabilities and their caregivers during the COVID-19 pandemic in Japan.
Journal: Journal of intellectual disabilities : JOID
Published: October 26, 2022
EVAHEART 2 with double cuff tipless inflow cannula is suitable for long-term support atrial switch operation in transposition of great arteries.
Journal: Journal of artificial organs : the official journal of the Japanese Society for Artificial Organs
Published: September 04, 2022
Germ-cell-specific transcriptome analysis illuminates the chromatin and ubiquitin pathway in autism spectrum disorders.
Journal: Autism research : official journal of the International Society for Autism Research
Published: April 04, 2022
Showing 1-10 of 10
Last Updated: 09/26/2026