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Page 1
GENETIC ETIOLOGY AND CLINICAL FEATURES OF ACHROMATOPSIA IN JAPAN.
Inooka T, Hayashi T, Tsunoda K, Kuniyoshi K, Kondo H, Mizobuchi K, Suga A, Iwata T, Yoshitake K, Kondo M, Goto K, Ota J, Kominami T, Nishiguchi KM, Ueno S. Inooka T, et al. Among authors: kuniyoshi k. Retina. 2024 Oct 1;44(10):1836-1844. doi: 10.1097/IAE.0000000000004170. Retina. 2024. PMID: 39287548
Reply.
Iwahashi C, Matsushita I, Kuniyoshi K, Kondo H, Kusaka S. Iwahashi C, et al. Among authors: kuniyoshi k. Retina. 2023 Jul 1;43(7):e43-e44. doi: 10.1097/IAE.0000000000003810. Retina. 2023. PMID: 37026808 No abstract available.
Optical coherence tomography findings of the peripheral retina in patients with congenital X-linked retinoschisis.
Nakajima A, Kuniyoshi K, Iwahashi C, Mano F, Hayashi T, Kondo H, Mizobuchi K, Matsushita I, Suga A, Yoshitake K, Nakano T, Iwata T, Matsumoto C, Kusaka S. Nakajima A, et al. Among authors: kuniyoshi k. Front Med (Lausanne). 2023 Nov 16;10:1280564. doi: 10.3389/fmed.2023.1280564. eCollection 2023. Front Med (Lausanne). 2023. PMID: 38034549 Free PMC article.
Genetic and Clinical Features of ABCA4-Associated Retinopathy in a Japanese Nationwide Cohort.
Mizobuchi K, Hayashi T, Tanaka K, Kuniyoshi K, Murakami Y, Nakamura N, Torii K, Mizota A, Sakai D, Maeda A, Kominami T, Ueno S, Kusaka S, Nishiguchi KM, Ikeda Y, Kondo M, Tsunoda K, Hotta Y, Nakano T. Mizobuchi K, et al. Among authors: kuniyoshi k. Am J Ophthalmol. 2024 Aug;264:36-43. doi: 10.1016/j.ajo.2024.03.007. Epub 2024 Mar 16. Am J Ophthalmol. 2024. PMID: 38499139 Free article.
Disease-specific variant interpretation highlighted the genetic findings in 2325 Japanese patients with retinitis pigmentosa and allied diseases.
Goto K, Koyanagi Y, Akiyama M, Murakami Y, Fukushima M, Fujiwara K, Iijima H, Yamaguchi M, Endo M, Hashimoto K, Ishizu M, Hirakata T, Mizobuchi K, Takayama M, Ota J, Sajiki AF, Kominami T, Ushida H, Fujita K, Kaneko H, Ueno S, Hayashi T, Terao C, Hotta Y, Murakami A, Kuniyoshi K, Kusaka S, Wada Y, Abe T, Nakazawa T, Ikeda Y, Momozawa Y, Sonoda KH, Nishiguchi KM. Goto K, et al. Among authors: kuniyoshi k. J Med Genet. 2024 Jun 20;61(7):613-620. doi: 10.1136/jmg-2023-109750. J Med Genet. 2024. PMID: 38499336
Necl-1/CADM3 regulates cone synapse formation in the mouse retina.
Kawashima R, Matsushita K, Mandai K, Sugita Y, Maruo T, Mizutani K, Midoh Y, Oguchi A, Murakawa Y, Kuniyoshi K, Sato R, Furukawa T, Nishida K, Takai Y. Kawashima R, et al. Among authors: kuniyoshi k. iScience. 2024 Mar 26;27(4):109577. doi: 10.1016/j.isci.2024.109577. eCollection 2024 Apr 19. iScience. 2024. PMID: 38623325 Free PMC article.
201 results