Rchr
J-GLOBAL ID：202101008942570281   Update date: Jan. 30, 2024

IIDA KIE

イイダ キエ | IIDA KIE
Affiliation and department：
Jikei University

About Jikei University


Research theme for competitive and other funds  (1)：
  • 2021 - 2024 筋原性前駆細胞に対する伸展誘導信号の抑制による「戻り」のない新規斜視治療法の開発
Papers (5)：
  • 林 孝彰, 近藤 寛之, 松下 五佳, 溝渕 圭, 馬場 昭典, 飯田 貴絵, 久保 寛之, 中野 匡. SLC38A8遺伝子に1塩基挿入変異を認めた常染色体劣性黄斑低形成の1例. 眼科臨床紀要. 2022. 15. 6. 416-416
  • Takaaki Hayashi, Hiroyuki Kondo, Itsuka Matsushita, Kei Mizobuchi, Akinori Baba, Kie Iida, Hiroyuki Kubo, Tadashi Nakano. Homozygous single nucleotide duplication of SLC38A8 in autosomal recessive foveal hypoplasia: The first Japanese case report. Documenta ophthalmologica. Advances in ophthalmology. 2021
  • Keiko Yamaguchi, Takaaki Hayashi, Akiko Kiriyama, Kie Iida, Shoyo Yoshimine, Yoichiro Masuda, Keigo Shikishima, Mitsuko Ariizumi, Genichiro Takahashi, Tadashi Nakano. Spontaneous Improvement of Visual Acuity in a 13-Year-Old Boy with Neuromyelitis Optica Spectrum Disorder. Neuro-ophthalmology (Aeolus Press). 2019. 43. 2. 114-119
  • Kie Iida, Yasuhiro Ohkuma, Takaaki Hayashi, Satoshi Katagiri, Takeshi Fujita, Kazushige Tsunoda, Hisashi Yamada, Hiroshi Tsuneoka. A novel heterozygous splice site OPA1 mutation causes exon 10 skipping in Japanese patients with dominant optic atrophy. Ophthalmic genetics. 2016. 37. 3. 354-6
  • 飯田 貴絵, 大熊 康弘, 林 孝彰, 藤田 剛史, 菊池 信介, 久保 寛之, 原 崇彰, 常岡 寛. 新規のOPA1遺伝子変異(V329L)を認めた常染色体優性視神経萎縮の1家系. 眼科臨床紀要. 2014. 7. 5. 385-385
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