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Spatial Functional Characteristics of East Asian Patients With Occult Macular Dystrophy (Miyake Disease); EAOMD Report No. 2.
Yang L, Joo K, Tsunoda K, Kondo M, Fujinami-Yokokawa Y, Arno G, Pontikos N, Liu X, Nakamura N, Kurihara T, Tsubota K, Iwata T, Li H, Zou X, Wu S, Sun Z, Ahn SJ, Kim MS, Mun YS, Park KH, Robson AG, Miyake Y, Woo SJ, Sui R, Fujinami K; East Asia Inherited Retinal Disease Society Study Group. Yang L, et al. Among authors: tsunoda k. Am J Ophthalmol. 2021 Jan;221:169-180. doi: 10.1016/j.ajo.2020.07.025. Epub 2020 Jul 21. Am J Ophthalmol. 2021. PMID: 32707201 Free article.
Transient macular dysfunction determined by focal macular electroretinogram.
Terauchi N, Fujinami K, Shinoda K, Tsunoda K, Hanazono G, Miyake Y, Inomata K. Terauchi N, et al. Among authors: tsunoda k. Br J Ophthalmol. 2007 Dec;91(12):1709-10. doi: 10.1136/bjo.2006.113373. Br J Ophthalmol. 2007. PMID: 18024815 Free PMC article. No abstract available.
Dominant mutations in RP1L1 are responsible for occult macular dystrophy.
Akahori M, Tsunoda K, Miyake Y, Fukuda Y, Ishiura H, Tsuji S, Usui T, Hatase T, Nakamura M, Ohde H, Itabashi T, Okamoto H, Takada Y, Iwata T. Akahori M, et al. Among authors: tsunoda k. Am J Hum Genet. 2010 Sep 10;87(3):424-9. doi: 10.1016/j.ajhg.2010.08.009. Am J Hum Genet. 2010. PMID: 20826268 Free PMC article.
667 results