Kanai A - Search Results

1

A novel mutation of M1S1 gene found in a Vietnamese patient with gelatinous droplike corneal dystrophy.

Ha NT, Chau HM, Cung le X, Thanh TK, Fujiki K, Murakami A, Kanai A. Ha NT, et al. Among authors: kanai a. Am J Ophthalmol. 2003 Mar;135(3):390-3. doi: 10.1016/s0002-9394(02)01952-9. Am J Ophthalmol. 2003. PMID: 12614764

2

Transthyretin Ser-44 mutation in a case with vitreous amyloidosis.

Murakami A, Fujiki K, Hasegawa S, Imamura S, Kawano H, Kanai A, Matsumoto T. Murakami A, et al. Among authors: kanai a. Am J Ophthalmol. 2002 Feb;133(2):272-3. doi: 10.1016/s0002-9394(01)01323-x. Am J Ophthalmol. 2002. PMID: 11812437

3

Heterozygous Ala137Pro mutation in keratin 12 gene found in Japanese with Meesmann's corneal dystrophy.

Takahashi K, Takahashi K, Murakami A, Okisaka S, Kimura T, Kanai A. Takahashi K, et al. Among authors: kanai a. Jpn J Ophthalmol. 2002 Nov-Dec;46(6):673-4. doi: 10.1016/s0021-5155(02)00563-4. Jpn J Ophthalmol. 2002. PMID: 12543196

4

A novel mutation of the TGFBI gene found in a Vietnamese family with atypical granular corneal dystrophy.

Ha NT, Cung le X, Chau HM, Thanh TK, Fujiki K, Murakami A, Kanai A. Ha NT, et al. Among authors: kanai a. Jpn J Ophthalmol. 2003 May-Jun;47(3):246-8. doi: 10.1016/s0021-5155(03)00019-4. Jpn J Ophthalmol. 2003. PMID: 12782158

5

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

6

Mutations in the CHST6 gene in patients with macular corneal dystrophy: immunohistochemical evidence of heterogeneity.

Iida-Hasegawa N, Furuhata A, Hayatsu H, Murakami A, Fujiki K, Nakayasu K, Kanai A. Iida-Hasegawa N, et al. Among authors: kanai a. Invest Ophthalmol Vis Sci. 2003 Aug;44(8):3272-7. doi: 10.1167/iovs.02-0910. Invest Ophthalmol Vis Sci. 2003. PMID: 12882769

7

Mutation analysis of the carbohydrate sulfotransferase gene in Vietnamese with macular corneal dystrophy.

Ha NT, Chau HM, Cung le X, Thanh TK, Fujiki K, Murakami A, Hiratsuka Y, Kanai A. Ha NT, et al. Among authors: kanai a. Invest Ophthalmol Vis Sci. 2003 Aug;44(8):3310-6. doi: 10.1167/iovs.03-0031. Invest Ophthalmol Vis Sci. 2003. PMID: 12882775

8

Identification of novel mutations of the CHST6 gene in Vietnamese families affected with macular corneal dystrophy in two generations.

Ha NT, Chau HM, Cung le X, Thanh TK, Fujiki K, Murakami A, Hiratsuka Y, Hasegawa N, Kanai A. Ha NT, et al. Among authors: kanai a. Cornea. 2003 Aug;22(6):508-11. doi: 10.1097/00003226-200308000-00004. Cornea. 2003. PMID: 12883341

9

Mutation analysis of the TGFBI gene in Vietnamese with granular and Avellino corneal dystrophy.

Cung le X, Ha NT, Chau HM, Thanh TK, Fujiki K, Murakami A, Hiratsuka Y, Kanai A. Cung le X, et al. Among authors: kanai a. Jpn J Ophthalmol. 2004 Jan-Feb;48(1):12-6. doi: 10.1007/s10384-003-0009-z. Jpn J Ophthalmol. 2004. PMID: 14767644

10

Compound heterozygous mutations of M1S1 gene in gelatinous droplike corneal dystrophy.

Tian X, Fujiki K, Li Q, Murakami A, Xie P, Kanai A, Wang W, Liu Z. Tian X, et al. Among authors: kanai a. Am J Ophthalmol. 2004 Mar;137(3):567-9. doi: 10.1016/j.ajo.2003.08.008. Am J Ophthalmol. 2004. PMID: 15013888

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