Hotta Y - Search Results

1

A new L527R mutation of the betaIGH3 gene in patients with lattice corneal dystrophy with deep stromal opacities.

Fujiki K, Hotta Y, Nakayasu K, Yokoyama T, Takano T, Yamaguchi T, Kanai A. Fujiki K, et al. Among authors: hotta y. Hum Genet. 1998 Sep;103(3):286-9. doi: 10.1007/s004390050818. Hum Genet. 1998. PMID: 9799082

2

Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP).

Fujiki K, Hotta Y, Hayakawa M, Sakuma H, Shiono T, Noro M, Sakuma T, Tamai M, Hikiji K, Kawaguchi R, et al. Fujiki K, et al. Among authors: hotta y. Jpn J Hum Genet. 1992 Jun;37(2):125-32. doi: 10.1007/BF01899733. Jpn J Hum Genet. 1992. PMID: 1391967

3

[Molecular biological study of the rhodopsin gene in Japanese patients with autosomal dominant retinitis pigmentosa].

Hotta Y, Shiono T, Hayakawa M, Hashimoto T, Kanai A, Nakajima A, Noro M, Sakuma T, Tamai M, Fujiki K. Hotta Y, et al. Nippon Ganka Gakkai Zasshi. 1992 Feb;96(2):237-42. Nippon Ganka Gakkai Zasshi. 1992. PMID: 1558021 Japanese.

4

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

5

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

6

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. Among authors: hotta y. Jinrui Idengaku Zasshi. 1991 Jun;36(2):143-7. doi: 10.1007/BF01876576. Jinrui Idengaku Zasshi. 1991. PMID: 1681125

7

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

8

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.

9

High resolution G-banding analysis in aniridia.

Hotta Y, Fujiki K, Ishida N, Kato K, Nakajima A, Takamatsu H. Hotta Y, et al. Ophthalmic Paediatr Genet. 1987 Nov;8(3):145-50. doi: 10.3109/13816818709031460. Ophthalmic Paediatr Genet. 1987. PMID: 2830569

10

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

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