Hotta Y - Search Results

1

Enhanced S-cone syndrome with subfoveal neovascularization.

Nakamura M, Hotta Y, Piao CH, Kondo M, Terasaki H, Miyake Y. Nakamura M, et al. Among authors: hotta y. Am J Ophthalmol. 2002 Apr;133(4):575-7. doi: 10.1016/s0002-9394(01)01428-3. Am J Ophthalmol. 2002. PMID: 11931802

2

High frequency of mitochondrial ND4 gene mutation in Japanese pedigrees with Leber hereditary optic neuropathy.

Nakamura M, Ara F, Yamada M, Hotta Y, Hayakawa M, Fujiki K, Kanai A, Sakai J, Inoue M, Yamamoto M, et al. Nakamura M, et al. Among authors: hotta y. Jpn J Ophthalmol. 1992;36(1):56-61. Jpn J Ophthalmol. 1992. PMID: 1635296

3

Clinical features of Japanese family with autosomal dominant retinitis pigmentosa caused by point mutation in codon 347 of rhodopsin gene.

Shiono T, Hotta Y, Noro M, Sakuma T, Tamai M, Hayakawa M, Hashimoto T, Fujiki K, Kanai A, Nakajima A. Shiono T, et al. Among authors: hotta y. Jpn J Ophthalmol. 1992;36(1):69-75. Jpn J Ophthalmol. 1992. PMID: 1635298

4

Diagnosis of Leber's optic neuropathy by means of polymerase chain reaction amplification.

Hotta Y, Hayakawa M, Saito K, Kanai A, Nakajima A, Fujiki K. Hotta Y, et al. Am J Ophthalmol. 1989 Nov 15;108(5):601-2. doi: 10.1016/0002-9394(89)90444-3. Am J Ophthalmol. 1989. PMID: 2817063 No abstract available.

5

Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA.

Hotta Y, Fujiki K, Hayakawa M, Nakajima A, Kanai A, Mashima Y, Hiida Y, Shinoda K, Yamada K, Oguchi Y, et al. Hotta Y, et al. Jpn J Ophthalmol. 1995;39(1):96-108. Jpn J Ophthalmol. 1995. PMID: 7643491

6

Clinical features of autosomal dominant retinitis pigmentosa with rhodopsin gene codon 17 mutation and retinal neovascularization in a Japanese patient.

Hayakawa M, Hotta Y, Imai Y, Fujiki K, Nakamura A, Yanashima K, Kanai A. Hayakawa M, et al. Among authors: hotta y. Am J Ophthalmol. 1993 Feb 15;115(2):168-73. doi: 10.1016/s0002-9394(14)73920-0. Am J Ophthalmol. 1993. PMID: 7679248

7

A high association with cone dystrophy in Fundus albipunctatus caused by mutations of the RDH5 gene.

Nakamura M, Hotta Y, Tanikawa A, Terasaki H, Miyake Y. Nakamura M, et al. Among authors: hotta y. Invest Ophthalmol Vis Sci. 2000 Nov;41(12):3925-32. Invest Ophthalmol Vis Sci. 2000. PMID: 11053295

8

Different mutation of the XLRS1 gene causes juvenile retinoschisis with retinal white flecks.

Hotta Y, Nakamura M, Okamoto Y, Nomura R, Terasaki H, Miyake Y. Hotta Y, et al. Br J Ophthalmol. 2001 Feb;85(2):238-9. doi: 10.1136/bjo.85.2.238. Br J Ophthalmol. 2001. PMID: 11225572 Free PMC article. No abstract available.

9

Late-onset form of lattice corneal dystrophy caused by leu527Arg mutation of the TGFBI gene.

Hirano K, Hotta Y, Nakamura M, Fujiki K, Kanai A, Yamamoto N. Hirano K, et al. Among authors: hotta y. Cornea. 2001 Jul;20(5):525-9. doi: 10.1097/00003226-200107000-00017. Cornea. 2001. PMID: 11413411

10

Triple anterior chamber after full-thickness lamellar keratoplasty for lattice corneal dystrophy.

Hirano K, Kojima T, Nakamura M, Hotta Y. Hirano K, et al. Among authors: hotta y. Cornea. 2001 Jul;20(5):530-3. doi: 10.1097/00003226-200107000-00018. Cornea. 2001. PMID: 11413412

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