Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kie Iida"'
Publikováno v:
American Journal of Case Reports. 3/9/2024, Vol. 25, p1-6. 6p.
Autor:
Itsuka Matsushita, Kie Iida, Akinori Baba, Hiroyuki Kubo, Kei Mizobuchi, Tadashi Nakano, Hiroyuki Kondo, Takaaki Hayashi
Publikováno v:
Documenta Ophthalmologica. 143:323-330
To characterize the clinical and genetic features of a Japanese male patient with foveal hypoplasia caused by a homozygous single nucleotide duplication in the SLC38A8 gene. We performed a comprehensive ophthalmic examination including full-field ele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3a321fced1e0560505a6c1f298b6e92
https://doi.org/10.1007/s10633-021-09842-y
https://doi.org/10.1007/s10633-021-09842-y
Autor:
Yoichiro Masuda, Takaaki Hayashi, Tadashi Nakano, Shoyo Yoshimine, Mitsuko Ariizumi, Akiko Kiriyama, Keigo Shikishima, Keiko Yamaguchi, Kie Iida, Genichiro Takahashi
Publikováno v:
Neuro-Ophthalmology. 43:114-119
Ophthalmic and MRI evaluations of a 13-year-old boy who reported loss of visual acuity in his right eye demonstrated the presence of unilateral optic neuritis. After serological tests showed positivity for anti-aquaporin 4 antibody, he was diagnosed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7134b967f80258a31a9430573b684cdc
https://doi.org/10.1080/01658107.2018.1483951
https://doi.org/10.1080/01658107.2018.1483951
Autor:
Yu, Imai, Taishi, Matsuura, Akira, Hisakane, Jun, Moritake, Shigehiro, Bando, Hiroki, Yamada, Hiroshi, Kiyota, Kie, Iida, Shin, Egawa
Publikováno v:
Hinyokika kiyo. Acta urologica Japonica. 65(2)
A 69-year-old male with the complaint of a cough was referred to our hospital from a clinic where he was found to have simultaneous metastases of the left kidney tumor. We performed left cytoreductive nephrectomy, and administered sunitinib after the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a8a098ee63ab0209f59427fb8bf5b39e
https://pubmed.ncbi.nlm.nih.gov/31067840
https://pubmed.ncbi.nlm.nih.gov/31067840
Autor:
Yasuhiro Ohkuma, Kazushige Tsunoda, Hisashi Yamada, Satoshi Katagiri, Takaaki Hayashi, Takeshi Fujita, Hiroshi Tsuneoka, Kie Iida
Publikováno v:
Ophthalmic genetics. 37(3)
Dominant optic atrophy (DOA) is the most common form of inherited optic neuropathy and characterized by slowly progressive visual loss, temporal pallor of optic discs, central visual field defects,...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe4d4f5a1d96b369b398b58e89e4f2c7
https://pubmed.ncbi.nlm.nih.gov/26854526
https://pubmed.ncbi.nlm.nih.gov/26854526