Yukiko Ihara
Nanakuma, 8140180, Japan
Last Updated: 09/26/2026
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Found 15 publications
Scalp EEG-recorded high-frequency oscillations can predict seizure activity in Panayiotopoulos syndrome.
Journal: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
Published: March 12, 2023
Coffin-Siris syndrome with bilateral macular dysplasia caused by a novel exonic deletion in ARID1B.
Journal: Congenital anomalies
Published: March 04, 2020
MeCP2_e2 partially compensates for lack of MeCP2_e1: A male case of Rett syndrome.
Journal: Molecular genetics & genomic medicine
Published: August 19, 2019
A clinical course of patient with Aicardi-Goutieres syndrome due to SAMHD1 gene abnormality.
Journal: No to hattatsu = Brain and development
Published: January 01, 2017
Abnormal γ-aminobutyric acid neurotransmission in a Kcnq2 model of early onset epilepsy.
Journal: Epilepsia
Published: May 01, 2015
A case of recurrent encephalopathy with SCN2A missense mutation.
Journal: Brain & development
Published: July 22, 2014
Clinical and genetic features of acute encephalopathy in children taking theophylline.
Journal: Brain & development
Published: May 21, 2014
A novel SCN1A mutation in a cytoplasmic loop in intractable juvenile myoclonic epilepsy without febrile seizures.
Journal: Epileptic disorders : international epilepsy journal with videotape
Published: May 21, 2014
Exacerbation of benign familial neonatal epilepsy induced by massive doses of phenobarbital and midazolam.
Journal: Pediatric neurology
Published: February 06, 2014
Last Updated: 09/26/2026