Kazuya Itomi
Obu, Japan
Last Updated: 09/26/2026
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Found 14 publications
Cerebrovascular diseases in two patients with entire NSD1 deletion.
Journal: Human genome variation
Published: February 18, 2021
Hyperpigmentation over the metacarpophalangeal joints and the malleoli in a case of hyaline fibromatosis syndrome with ANTXR2 mutations.
Journal: Journal of the European Academy of Dermatology and Venereology : JEADV
Published: September 04, 2015
The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy.
Journal: Brain & development
Published: March 12, 2015
Immediate suppression of seizure clusters by corticosteroids in PCDH19 female epilepsy.
Journal: Seizure
Published: November 04, 2014
PET in infancy predicts long-term outcome during adolescence in cryptogenic West syndrome.
Journal: AJNR. American journal of neuroradiology
Published: March 29, 2014
Microarray and FISH-based genotype-phenotype analysis of 22 Japanese patients with Wolf-Hirschhorn syndrome.
Journal: American journal of medical genetics. Part A
Published: April 27, 2013
Last Updated: 09/26/2026