Sato M - 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: sato m. Sci Rep. 2018 May 29;8(1):8279. doi: 10.1038/s41598-018-26524-z. Sci Rep. 2018. PMID: 29844330 Free PMC article.

2

Chronic angle closure glaucoma secondary to frail zonular fibres and spherophakia.

Asaoka R, Kato M, Suami M, Usami Y, Hotta Y, Sato M. Asaoka R, et al. Among authors: sato m. Acta Ophthalmol Scand. 2003 Oct;81(5):533-5. doi: 10.1034/j.1600-0420.2003.00129.x. Acta Ophthalmol Scand. 2003. PMID: 14510805 Free article.

3

A case of sectorial benign flecked retina.

Tsuchiya T, Kato M, Tomita N, Koide K, Hata N, Sato M, Hotta Y, Ueno M, Nakamura M, Miyake Y. Tsuchiya T, et al. Among authors: sato m. Jpn J Ophthalmol. 2004 Jan-Feb;48(1):72-4. doi: 10.1007/s10384-003-0002-6. Jpn J Ophthalmol. 2004. PMID: 14767656

4

Multicentric atypical teratoid/rhabdoid tumors occurring in the eye and fourth ventricle of an infant: case report.

Fujita M, Sato M, Nakamura M, Kudo K, Nagasaka T, Mizuno M, Amano E, Okamoto Y, Hotta Y, Hatano H, Nakahara N, Wakabayashi T, Yoshida J. Fujita M, et al. Among authors: sato m. J Neurosurg. 2005 Apr;102(3 Suppl):299-302. doi: 10.3171/ped.2005.102.3.0299. J Neurosurg. 2005. PMID: 15881754

5

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: sato m. 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.

6

Early detection of thinning of retinal nerve fiber layer in glaucomatous eyes by optical coherence tomography 3000: analysis of retinal nerve fiber layer corresponding to the preserved hemivisual field.

Asaoka R, Ishii R, Kyu N, Hotta Y, Sato M. Asaoka R, et al. Among authors: sato m. Ophthalmic Res. 2006;38(1):29-35. doi: 10.1159/000088549. Epub 2005 Sep 23. Ophthalmic Res. 2006. PMID: 16192746

7

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: sato m. 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

8

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: sato m. Ophthalmic Genet. 2008 Mar;29(1):29-32. doi: 10.1080/13816810701663535. Ophthalmic Genet. 2008. PMID: 18363170

9

Superior oblique palsy with class III tendon anomaly.

Sato M, Iwata EA, Takai Y, Hikoya A, Koide YM. Sato M, et al. 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

10

Central corneal thickness in Japanese children.

Hikoya A, Sato M, Tsuzuki K, Koide YM, Asaoka R, Hotta Y. Hikoya A, et al. Among authors: sato m. 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

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