The findings of optical coherence tomography of retinal degeneration in relation to the morphological and electroretinographic features in RPE65-/- mice.

Autor: Reiko Tanabu, Kota Sato, Natsuki Monai, Kodai Yamauchi, Takayuki Gonome, Yuting Xie, Shizuka Takahashi, Sei-Ichi Ishiguro, Mitsuru Nakazawa

Publikováno v: PLoS ONE, Vol 14, Iss 1, p e0210439 (2019)

PURPOSE:Mutations of the gene encoding RPE65 cause Leber congenital amaurosis (LCA) retinitis pigmentosa (RP). The optical coherence tomography (OCT) is increasingly utilized to noninvasively evaluate various types of retinal diseases, including RP.

Externí odkaz: https://doaj.org/article/922dd2f4bec4409aa1f8d45988501137

Intraoperative Adjunctive Mitomycin C and Cryotherapy for Recurrent Conjunctival Papillary Sebaceous Carcinoma

Autor: Satoko Morohashi, Katsunori Yokoi, Mitsuru Nakazawa, Akira Kurose, Hideaki Hirai, Takayuki Gonome, Reiko Tanabu, Natsuki Monai, Satoshi Urushidate

Publikováno v: Case Reports in Ophthalmology
Case Reports in Ophthalmology, Vol 9, Iss 1, Pp 221-226 (2018)

Purpose: To report a case of recurrent conjunctival papillary sebaceous carcinoma that was successfully treated by a combination of surgical resection, intraoperative topical mitomycin C application, and cryotherapy. Observations: A woman in her 80s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ad78eaa06d3758a41c6a51d785ef9d4
http://europepmc.org/articles/PMC5903128

The findings of optical coherence tomography of retinal degeneration in relation to the morphological and electroretinographic features in RPE65−/− mice

Autor: Kota Sato, Yuting Xie, Shizuka Takahashi, Sei Ichi Ishiguro, Natsuki Monai, Reiko Tanabu, Kodai Yamauchi, Mitsuru Nakazawa, Takayuki Gonome

Publikováno v: PLoS ONE, Vol 14, Iss 1, p e0210439 (2019)
PLoS ONE

Purpose Mutations of the gene encoding RPE65 cause Leber congenital amaurosis (LCA) retinitis pigmentosa (RP). The optical coherence tomography (OCT) is increasingly utilized to noninvasively evaluate various types of retinal diseases, including RP.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ecca72069c5b69bd0b32c0ce97c40f7
https://doi.org/10.1371/journal.pone.0210439

A small trinucleotide expansion in the TBP gene gives rise to a sporadic case of SCA17 with abnormal putaminal findings on MRI

Autor: Yukiko Yamamoto-Watanabe, Mikio Shoji, Yasuhito Wakasaya, Yoshio Ikeda, Mandy Jackson, Chieko Suzuki, Yusuke Seino, Etsuro Matsubara, Mitsunori Watanabe, Takeshi Kawarabayashi, Natsuki Monai, Masahiko Tomiyama, Yasuo Miki, Tamaki Kimura

Publikováno v: Watanabe, M, Monai, N, Jackson, M, Yamamoto-Watanabe, Y, Ikeda, Y, Suzuki, C, Tomiyama, M, Kawarabayashi, T, Kimura, T, Seino, Y, Wakasaya, Y, Miki, Y, Matsubara, E & Shoji, M 2008, ' A Small Trinucleotide Expansion in the TBP Gene Gives Rise to a Sporadic Case of SCA17 with Abnormal Putaminal Findings on MRI ', Internal Medicine, vol. 47, no. 24, pp. 2179-2182 . https://doi.org/10.2169/internalmedicine.47.1499

A Japanese woman developed gait disturbances at 25 years of age, and subsequently underwent gradual changes in her personality. By the age of 42, she showed clear signs of dementia and cerebellar ataxia, and displayed behavioral abnormalities, chorei

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a593347efa64cad51351e0fae99d4a9
https://pubmed.ncbi.nlm.nih.gov/19075547