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Gene|December 14, 2004
Identification, expression analysis and polymorphism of a novel RLTPR gene encoding a RGD motif, tropomodulin domain and proline/leucine-rich regionsYasunari Matsuzaka, Koichi Okamoto, Tomotaka Mabuchi, et al.
Immunogenetics|March 12, 2013
Improved loop-mediated isothermal amplification for HLA-DRB1 genotyping using RecA and a restriction enzyme for enhanced amplification specificityShigeki Mitsunaga, Sayoko Shimizu, Yuko Okudaira, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 30, 2021
Telemedicine in epilepsy management during the coronavirus disease 2019 pandemicKenjiro Kikuchi, Shin-Ichiro Hamano, Ayumi Horiguchi, et al.
Seizure|December 20, 2024
Elementary school enrollment after ACTH therapy for patients with infantile epileptic spasms syndromeRyuki Matsuura, Shin-Ichiro Hamano, Yuko Hirata, et al.
Brain & Development|April 22, 2026
Dynamic thalamo-cortical perfusion changes in myoclonic-atonic seizures captured by ictal technetium-99m ethyl cysteinate dimer single-photon emission computed tomography: A case reportRyuki Matsuura, Shin-Ichiro Hamano, Azusa Oba, et al.
Optics Letters|April 2, 2015
Low-loss partial rib polarization rotator consisting only of silicon core and silica claddingKazuhiro Goi, Akira Oka, Hiroyuki Kusaka, et al.
Brain & Development|September 28, 2025
Serum matrix metallopeptidase-9 levels in patients with infantile epileptic spasms syndrome before and after the initiation of vigabatrin therapyRyuki Matsuura, Shin-Ichiro Hamano, Atsuro Daida, et al.
Cell Communication and Signaling : CCS|June 2, 2023
LOX-1 mediates inflammatory activation of microglial cells through the p38-MAPK/NF-κB pathways under hypoxic-ischemic conditionsYoshinori Aoki, Hongmei Dai, Fumika Furuta, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 20, 2016
Systemic lupus erythematosus presenting with mixed-type fulminant autoimmune hemolytic anemiaYoko Hirano, Takaaki Itonaga, Hiroki Yasudo, et al.
Molecular Genetics & Genomic Medicine|December 29, 2019
Noonan syndrome-associated biallelic LZTR1 mutations cause cardiac hypertrophy and vascular malformations in zebrafishYu Nakagama, Norihiko Takeda, Seishi Ogawa, et al.
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