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Vitreoretinal traction maculopathy caused by retinal diseases.
Asami T, Terasaki H, Hirose H, Suzuki T, Horio N, Miyake Y. Asami T, et al. Among authors: miyake y. Am J Ophthalmol. 2001 Jan;131(1):134-6. doi: 10.1016/s0002-9394(00)00856-4. Am J Ophthalmol. 2001. PMID: 11162993
Multicenter genetic study of retinitis pigmentosa in Japan: II. Prevalence of autosomal recessive retinitis pigmentosa.
Hayakawa M, Fujiki K, Kanai A, Matsumura M, Honda Y, Sakaue H, Tamai M, Sakuma T, Tokoro T, Yura T, Kubota N, Kawano S, Matsui M, Yuzawa M, Oguchi Y, Akeo K, Adachi E, Kimura T, Miyake Y, Horiguchi M, Wakabayashi K, Ishizaka N, Koizumi K, Uyama M, Ohba N, et al. Hayakawa M, et al. Among authors: miyake y. Jpn J Ophthalmol. 1997 Jan-Feb;41(1):7-11. doi: 10.1016/s0021-5155(96)00019-6. Jpn J Ophthalmol. 1997. PMID: 9147181
X-linked retinoschisis with point mutations in the XLRS1 gene.
Inoue Y, Yamamoto S, Okada M, Tsujikawa M, Inoue T, Okada AA, Kusaka S, Saito Y, Wakabayashi K, Miyake Y, Fujikado T, Tano Y. Inoue Y, et al. Among authors: miyake y. Arch Ophthalmol. 2000 Jan;118(1):93-6. doi: 10.1001/archopht.118.1.93. Arch Ophthalmol. 2000. PMID: 10636421
Unilateral cone dysfunction with bull's eye maculopathy.
Nomura R, Kondo M, Tanikawa A, Yamamoto N, Terasaki H, Miyake Y. Nomura R, et al. Among authors: miyake y. Ophthalmology. 2001 Jan;108(1):49-53. doi: 10.1016/s0161-6420(00)00450-4. Ophthalmology. 2001. PMID: 11150264
Multicenter genetic study of retinitis pigmentosa in Japan: I. Genetic heterogeneity in typical retinitis pigmentosa.
Hayakawa M, Fujiki K, Kanai A, Matsumura M, Honda Y, Sakaue H, Tamai M, Sakuma T, Tokoro T, Yura T, Kubota N, Kawano S, Matsui M, Yuzawa M, Oguchi Y, Akeo K, Adachi E, Kimura T, Miyake Y, Horiguchi M, Wakabayashi K, Ishizaka N, Koizumi K, Uyama M, Ohba N, et al. Hayakawa M, et al. Among authors: miyake y. Jpn J Ophthalmol. 1997 Jan-Feb;41(1):1-6. doi: 10.1016/s0021-5155(96)00018-4. Jpn J Ophthalmol. 1997. PMID: 9147180
2,273 results