Miyazawa A - Search Results

1

Higher incidence of carotid stenosis in patients with central retinal artery occlusion.

Miyazawa A, Inoue M, Yamada S, Hirota K, Sano RY, Nishiyama K, Hirakata A. Miyazawa A, et al. Acta Ophthalmol. 2011 Jun;89(4):e378-9. doi: 10.1111/j.1755-3768.2010.01893.x. Epub 2010 Apr 9. Acta Ophthalmol. 2011. PMID: 20384592 Free article. No abstract available.

2

Expression of inhibin alpha by stromal cells of retinal angiomas excised from a patient with von Hippel-Lindau disease.

Miyazawa A, Inoue M, Hirakata A, Okada AA, Iihara K, Fujioka Y. Miyazawa A, et al. Jpn J Ophthalmol. 2009 Sep;53(5):501-5. doi: 10.1007/s10384-009-0699-y. Epub 2009 Oct 22. Jpn J Ophthalmol. 2009. PMID: 19847606

3

Mutation spectrum of the CYP1B1 gene for congenital glaucoma in the Japanese population.

Fuse N, Miyazawa A, Takahashi K, Noro M, Nakazawa T, Nishida K. Fuse N, et al. Among authors: miyazawa a. Jpn J Ophthalmol. 2010 Jan;54(1):1-6. doi: 10.1007/s10384-009-0769-1. Epub 2010 Feb 12. Jpn J Ophthalmol. 2010. PMID: 20151268

4

Aqueous flare and cell measurement using laser in endogenous uveitis patients.

Ohara K, Okubo A, Miyazawa A, Miyamoto T, Sasaki H, Oshima F. Ohara K, et al. Among authors: miyazawa a. Jpn J Ophthalmol. 1989;33(3):265-70. Jpn J Ophthalmol. 1989. PMID: 2796007

5

Polymorphisms in Complement Factor H and Hemicentin-1 genes in a Japanese population with dry-type age-related macular degeneration.

Fuse N, Miyazawa A, Mengkegale M, Yoshida M, Wakusawa R, Abe T, Tamai M. Fuse N, et al. Among authors: miyazawa a. Am J Ophthalmol. 2006 Dec;142(6):1074-6. doi: 10.1016/j.ajo.2006.07.030. Epub 2006 Aug 31. Am J Ophthalmol. 2006. PMID: 17157600

6

Association between primary open-angle glaucoma and WDR36 DNA sequence variants in Japanese.

Miyazawa A, Fuse N, Mengkegale M, Ryu M, Seimiya M, Wada Y, Nishida K. Miyazawa A, et al. Mol Vis. 2007 Oct 9;13:1912-9. Mol Vis. 2007. PMID: 17960130

7

Presence of myocilin sequence variants in Japanese patients with open-angle glaucoma.

Mengkegale M, Fuse N, Miyazawa A, Takahashi K, Seimiya M, Yasui T, Tamai M, Nakazawa T, Nishida K. Mengkegale M, et al. Among authors: miyazawa a. Mol Vis. 2008 Mar 4;14:413-7. Mol Vis. 2008. PMID: 18334962 Free PMC article.

8

Evaluation of LOXL1 polymorphisms in eyes with exfoliation glaucoma in Japanese.

Fuse N, Miyazawa A, Nakazawa T, Mengkegale M, Otomo T, Nishida K. Fuse N, et al. Among authors: miyazawa a. Mol Vis. 2008 Jul 21;14:1338-43. Mol Vis. 2008. PMID: 18648524 Free PMC article.

9

Polymorphisms in ARMS2 (LOC387715) and LOXL1 genes in the Japanese with age-related macular degeneration.

Fuse N, Mengkegale M, Miyazawa A, Abe T, Nakazawa T, Wakusawa R, Nishida K. Fuse N, et al. Among authors: miyazawa a. Am J Ophthalmol. 2011 Mar;151(3):550-6.e1. doi: 10.1016/j.ajo.2010.08.048. Epub 2011 Jan 13. Am J Ophthalmol. 2011. PMID: 21236409

10

Association of HK2 and NCK2 with normal tension glaucoma in the Japanese population.

Shi D, Funayama T, Mashima Y, Takano Y, Shimizu A, Yamamoto K, Mengkegale M, Miyazawa A, Yasuda N, Fukuchi T, Abe H, Ideta H, Nishida K, Nakazawa T, Richards JE, Fuse N. Shi D, et al. Among authors: miyazawa a. PLoS One. 2013;8(1):e54115. doi: 10.1371/journal.pone.0054115. Epub 2013 Jan 22. PLoS One. 2013. PMID: 23349798 Free PMC article.

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