Kanai A - Search Results

1

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. Among authors: kanai a. Jpn J Ophthalmol. 1995;39(1):96-108. Jpn J Ophthalmol. 1995. PMID: 7643491

2

OPA1 gene mutations in Japanese patients with bilateral optic atrophy unassociated with mitochondrial DNA mutations at nt 11778, 3460, and 14484.

Yamada T, Hayasaka S, Matsumoto M, Budu, Esa T, Hayasaka Y, Endo M, Nagaki Y, Fujiki K, Murakami A, Kanai A. Yamada T, et al. Among authors: kanai a. Jpn J Ophthalmol. 2003 Jul-Aug;47(4):409-11. doi: 10.1016/s0021-5155(03)00056-x. Jpn J Ophthalmol. 2003. PMID: 12842213

3

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: kanai a. Jpn J Ophthalmol. 1992;36(1):56-61. Jpn J Ophthalmol. 1992. PMID: 1635296

4

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: kanai a. Jpn J Ophthalmol. 1992;36(1):69-75. Jpn J Ophthalmol. 1992. PMID: 1635298

5

[A trial of molecular diagnosis in Leber's optic neuropathy].

Ara F, Hotta Y, Hayakawa M, Yanashima K, Kanai A, Fujiki K. Ara F, et al. Among authors: kanai a. Nippon Ganka Gakkai Zasshi. 1991 Aug;95(8):715-20. Nippon Ganka Gakkai Zasshi. 1991. PMID: 1950826 Review. Japanese.

6

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. Among authors: kanai a. 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.

7

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: kanai a. Am J Ophthalmol. 1993 Feb 15;115(2):168-73. doi: 10.1016/s0002-9394(14)73920-0. Am J Ophthalmol. 1993. PMID: 7679248

8

A multicenter study of typical retinitis pigmentosa in Japan.

Hayakawa M, Matsumura M, Ohba N, Matsui M, Fujiki K, Kanai A, Tamai M, Shiono T, Tokoro T, Akazawa Y, et al. Hayakawa M, et al. Among authors: kanai a. Jpn J Ophthalmol. 1993;37(2):156-64. Jpn J Ophthalmol. 1993. PMID: 8230840

9

An atypical Leber's hereditary optic neuropathy with the 11778 mutation.

Hotta Y, Hayakawa M, Fujiki K, Shinohara K, Sado K, Kanai A, Yanashima K. Hotta Y, et al. Among authors: kanai a. Br J Ophthalmol. 1993 Nov;77(11):748-50. doi: 10.1136/bjo.77.11.748. Br J Ophthalmol. 1993. PMID: 8280696 Free PMC article. No abstract available.

10

Missense mutation of rhodopsin gene codon 15 found in Japanese autosomal dominant retinitis pigmentosa.

Fujiki K, Hotta Y, Murakami A, Yoshii M, Hayakawa M, Ichikawa T, Takeda M, Akeo K, Okisaka S, Kanai A. Fujiki K, et al. Among authors: kanai a. Jpn J Hum Genet. 1995 Sep;40(3):271-7. doi: 10.1007/BF01876186. Jpn J Hum Genet. 1995. PMID: 8527802

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