Akie Miyamoto
Asahikawa, Japan
Last Updated: 09/26/2026
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Found 10 publications
GRIA3 p.Met661Thr variant in a female with developmental epileptic encephalopathy.
Journal: Human genome variation
Published: November 24, 2022
Severe gastrointestinal symptoms caused by a novel DDX3X variant.
Journal: European journal of medical genetics
Published: March 26, 2020
Genitopatellar syndrome: the first reported case in Japan.
Journal: Human genome variation
Published: November 15, 2017
Specific HLA genotypes confer susceptibility to acute necrotizing encephalopathy.
Journal: Genes and immunity
Published: May 19, 2016
Clinical and genetic features of acute encephalopathy in children taking theophylline.
Journal: Brain & development
Published: May 21, 2014
Treatment with ramelteon for sleep disturbance in severely disabled children and young adults
Journal: No to hattatsu = Brain and development
Published: December 10, 2013
FOXG1 mutations in Japanese patients with the congenital variant of Rett syndrome.
Journal: Clinical genetics
Published: December 02, 2011
Surgical management for intractable aspiration in handicapped children
Journal: No to hattatsu = Brain and development
Published: January 29, 2009
Evaluation of social functioning ability of disabled children
Journal: No to hattatsu = Brain and development
Published: September 22, 2006
Showing 1-10 of 10
Last Updated: 09/26/2026