Hikoya A - Search Results

1

Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing.

Hosono K, Nishina S, Yokoi T, Katagiri S, Saitsu H, Kurata K, Miyamichi D, Hikoya A, Mizobuchi K, Nakano T, Minoshima S, Fukami M, Kondo H, Sato M, Hayashi T, Azuma N, Hotta Y. Hosono K, et al. Among authors: hikoya a. Sci Rep. 2018 May 29;8(1):8279. doi: 10.1038/s41598-018-26524-z. Sci Rep. 2018. PMID: 29844330 Free PMC article.

2

DNA analysis for diagnosis of x-linked juvenile retinoschisis when clinical examination is difficult in a young child.

Kawano T, Sato M, Hikoya A, Nishimura K, Hotta Y. Kawano T, et al. Among authors: hikoya a. Jpn J Ophthalmol. 2005 May-Jun;49(3):268-70. doi: 10.1007/s10384-004-0186-4. Jpn J Ophthalmol. 2005. PMID: 15944839 No abstract available.

3

Three novel mutations of the PAX6 gene in Japanese aniridia patients.

Kawano T, Wang C, Hotta Y, Sato M, Iwata-Amano E, Hikoya A, Fujita N, Koyama N, Shirai S, Azuma N, Ohtsubo M, Shimizu N, Minoshima S. Kawano T, et al. Among authors: hikoya a. J Hum Genet. 2007;52(7):571-574. doi: 10.1007/s10038-007-0153-2. Epub 2007 Jun 14. J Hum Genet. 2007. PMID: 17568989

4

Novel RDH5 mutation in family with mother having fundus albipunctatus and three children with retinitis pigmentosa.

Wang C, Nakanishi N, Ohishi K, Hikoya A, Koide K, Sato M, Nakamura M, Hotta Y, Minoshima S. Wang C, et al. Among authors: hikoya a. Ophthalmic Genet. 2008 Mar;29(1):29-32. doi: 10.1080/13816810701663535. Ophthalmic Genet. 2008. PMID: 18363170

5

Superior oblique palsy with class III tendon anomaly.

Sato M, Iwata EA, Takai Y, Hikoya A, Koide YM. Sato M, et al. Among authors: hikoya a. Am J Ophthalmol. 2008 Sep;146(3):385-394. doi: 10.1016/j.ajo.2008.05.013. Epub 2008 Jul 14. Am J Ophthalmol. 2008. PMID: 18621358

6

Central corneal thickness in Japanese children.

Hikoya A, Sato M, Tsuzuki K, Koide YM, Asaoka R, Hotta Y. Hikoya A, et al. Jpn J Ophthalmol. 2009 Jan;53(1):7-11. doi: 10.1007/s10384-008-0619-6. Epub 2009 Jan 30. Jpn J Ophthalmol. 2009. PMID: 19184302

7

Magnetic resonance imaging of the medial rectus muscle of patients with consecutive exotropia after medial rectus muscle recession.

Negishi T, Hikoya A, Isoda H, Tsuchiya Y, Sawada M, Hotta Y, Sato M. Negishi T, et al. Among authors: hikoya a. Ophthalmology. 2010 Oct;117(10):1876-82. doi: 10.1016/j.ophtha.2010.02.006. Epub 2010 Jun 11. Ophthalmology. 2010. PMID: 20541264

8

Case of Japanese patient with x-linked ocular albinism associated with GPR143 gene mutation.

Ohtsubo M, Sato M, Hikoya A, Hosono K, Minoshima S, Hotta Y. Ohtsubo M, et al. Among authors: hikoya a. Jpn J Ophthalmol. 2010 Nov;54(6):624-6. doi: 10.1007/s10384-010-0872-3. Jpn J Ophthalmol. 2010. PMID: 21274678 No abstract available.

9

Case of Japanese patient with x-linked ocular albinism associated with GPR143 gene mutation.

Ohtsubo M, Sato M, Hikoya A, Hosono K, Minoshima S, Hotta Y. Ohtsubo M, et al. Among authors: hikoya a. Jpn J Ophthalmol. 2010 Nov;54(6):624-6. Jpn J Ophthalmol. 2010. PMID: 21348135 No abstract available.

10

A case of aniridia with unilateral Peters anomaly.

Sawada M, Sato M, Hikoya A, Wang C, Minoshima S, Azuma N, Hotta Y. Sawada M, et al. Among authors: hikoya a. J AAPOS. 2011 Feb;15(1):104-6. doi: 10.1016/j.jaapos.2010.11.006. J AAPOS. 2011. PMID: 21397818

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