Fujiki K - Search Results

1

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: fujiki k. 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.

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

3

A mutation of mitochondrial DNA in Japanese families with Leber's hereditary optic neuropathy.

Fujiki K, Hotta Y, Hayakawa M, Saito K, Ara F, Ueda S, Goto T, Ishida M, Yanashima K, Shiono T, et al. Fujiki K, et al. Jinrui Idengaku Zasshi. 1991 Jun;36(2):143-7. doi: 10.1007/BF01876576. Jinrui Idengaku Zasshi. 1991. PMID: 1681125

4

[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: fujiki k. Nippon Ganka Gakkai Zasshi. 1991 Aug;95(8):715-20. Nippon Ganka Gakkai Zasshi. 1991. PMID: 1950826 Review. Japanese.

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. Among authors: fujiki k. 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: fujiki k. 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

[Leber's hereditary optic neuropathy with onset at the age of 54 years].

Nakamura N, Furukawa Y, Fujiki K, Hayakawa M, Mizuno Y. Nakamura N, et al. Among authors: fujiki k. Rinsho Shinkeigaku. 1994 Mar;34(3):258-60. Rinsho Shinkeigaku. 1994. PMID: 8200145 Japanese.

8

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: fujiki k. 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.

9

Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathy.

Matsumoto M, Hayasaka S, Kadoi C, Hotta Y, Fujiki K, Fujimaki T, Takeda M, Ishida N, Endo S, Kanai A. Matsumoto M, et al. Among authors: fujiki k. Ophthalmic Genet. 1999 Sep;20(3):153-60. doi: 10.1076/opge.20.3.153.2281. Ophthalmic Genet. 1999. PMID: 10520236

10

Q118X mutation of M1S1 gene caused gelatinous drop-like corneal dystrophy: the P501T of BIGH3 gene found in a family with gelatinous drop-like corneal dystrophy.

Ha NT, Fujiki K, Hotta Y, Nakayasu K, Kanai A. Ha NT, et al. Among authors: fujiki k. Am J Ophthalmol. 2000 Jul;130(1):119-20. doi: 10.1016/s0002-9394(00)00596-1. Am J Ophthalmol. 2000. PMID: 11004271

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