Sato M - Search Results

1

Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis Pigmentosa.

Tachibana N, Hosono K, Nomura S, Arai S, Torii K, Kurata K, Sato M, Shimakawa S, Azuma N, Ogata T, Wada Y, Okamoto N, Saitsu H, Nishina S, Hotta Y. Tachibana N, et al. Among authors: sato m. Genes (Basel). 2022 Feb 16;13(2):359. doi: 10.3390/genes13020359. Genes (Basel). 2022. PMID: 35205402 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

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

6

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

7

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

8

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

9

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: sato m. Ophthalmology. 2010 Oct;117(10):1876-82. doi: 10.1016/j.ophtha.2010.02.006. Epub 2010 Jun 11. Ophthalmology. 2010. PMID: 20541264

10

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: sato m. 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.

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