Author/Creator: Iida, Kie - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Iida, Kie

1. A novel heterozygous splice site OPA1 mutation causes exon 10 skipping in Japanese patients with dominant optic atrophy. (2nd July 2016)

Authors:: Iida, Kie; Ohkuma, Yasuhiro; Hayashi, Takaaki; Katagiri, Satoshi; Fujita, Takeshi; Tsunoda, Kazushige; Yamada, Hisashi; Tsuneoka, Hiroshi
Journal:: Ophthalmic genetics
Issue:: Volume 37:Number 3(2016)
Page Start:: 354
Record Type:: Journal Article
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2. Spontaneous Improvement of Visual Acuity in a 13-Year-Old Boy with Neuromyelitis Optica Spectrum Disorder. (4th March 2019)

Authors:: Yamaguchi, Keiko; Hayashi, Takaaki; Kiriyama, Akiko; Iida, Kie; Yoshimine, Shoyo; Masuda, Yoichiro; Shikishima, Keigo; Ariizumi, Mitsuko; Takahashi, Genichiro; Nakano, Tadashi
Journal:: Neuro-ophthalmology
Issue:: Volume 43:Number 2(2019)
Page Start:: 114
Record Type:: Journal Article
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