Wada Y - Search Results

1

Age at onset curves of retinitis pigmentosa.

Tsujikawa M, Wada Y, Sukegawa M, Sawa M, Gomi F, Nishida K, Tano Y. Tsujikawa M, et al. Among authors: wada y. Arch Ophthalmol. 2008 Mar;126(3):337-40. doi: 10.1001/archopht.126.3.337. Arch Ophthalmol. 2008. PMID: 18332312

2

Screening of the MERTK gene for mutations in Japanese patients with autosomal recessive retinitis pigmentosa.

Tada A, Wada Y, Sato H, Itabashi T, Kawamura M, Tamai M, Nishida K. Tada A, et al. Among authors: wada y. Mol Vis. 2006 May 9;12:441-4. Mol Vis. 2006. PMID: 16710167 Free article.

3

A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa.

Nishiguchi KM, Miya F, Mori Y, Fujita K, Akiyama M, Kamatani T, Koyanagi Y, Sato K, Takigawa T, Ueno S, Tsugita M, Kunikata H, Cisarova K, Nishino J, Murakami A, Abe T, Momozawa Y, Terasaki H, Wada Y, Sonoda KH, Rivolta C, Tsunoda T, Tsujikawa M, Ikeda Y, Nakazawa T. Nishiguchi KM, et al. Among authors: wada y. Commun Biol. 2021 Jan 29;4(1):140. doi: 10.1038/s42003-021-01662-9. Commun Biol. 2021. PMID: 33514863 Free PMC article.

4

Retinitis pigmentosa associated with ectopia lentis.

Sato H, Wada Y, Abe T, Kawamura M, Wakusawa R, Tamai M. Sato H, et al. Among authors: wada y. Arch Ophthalmol. 2002 Jun;120(6):852-4. Arch Ophthalmol. 2002. PMID: 12049599 No abstract available.

5

Case of orbital sebaceous carcinoma developing twenty-seven years after enucleation.

Tanaka T, Sato H, Tada A, Moriya T, Wada Y, Nishida K. Tanaka T, et al. Among authors: wada y. Jpn J Ophthalmol. 2008 Jul-Aug;52(4):344-345. doi: 10.1007/s10384-008-0552-8. Epub 2008 Sep 5. Jpn J Ophthalmol. 2008. PMID: 18773280 No abstract available.

6

Arrestin gene mutations in autosomal recessive retinitis pigmentosa.

Nakazawa M, Wada Y, Tamai M. Nakazawa M, et al. Among authors: wada y. Arch Ophthalmol. 1998 Apr;116(4):498-501. doi: 10.1001/archopht.116.4.498. Arch Ophthalmol. 1998. PMID: 9565049

7

Autosomal dominant macular degeneration associated with 208delG mutation in the FSCN2 gene.

Wada Y, Abe T, Itabashi T, Sato H, Kawamura M, Tamai M. Wada Y, et al. Arch Ophthalmol. 2003 Nov;121(11):1613-20. doi: 10.1001/archopht.121.11.1613. Arch Ophthalmol. 2003. PMID: 14609921

8

Novel 2336-2337delCT mutation in RP1 gene in a Japanese family with autosomal dominant retinitis pigmentosa.

Kawamura M, Wada Y, Noda Y, Itabashi T, Ogawa S, Sato H, Tanaka K, Ishibashi T, Tamai M. Kawamura M, et al. Among authors: wada y. Am J Ophthalmol. 2004 Jun;137(6):1137-9. doi: 10.1016/j.ajo.2003.12.037. Am J Ophthalmol. 2004. PMID: 15183808

9

Screening for mutations in the IMPDH1 gene in Japanese patients with autosomal dominant retinitis pigmentosa.

Wada Y, Tada A, Itabashi T, Kawamura M, Sato H, Tamai M. Wada Y, et al. Am J Ophthalmol. 2005 Jul;140(1):163-5. doi: 10.1016/j.ajo.2005.01.017. Am J Ophthalmol. 2005. PMID: 16038673

10

Mutations in the pre-mRNA splicing gene, PRPF31, in Japanese families with autosomal dominant retinitis pigmentosa.

Sato H, Wada Y, Itabashi T, Nakamura M, Kawamura M, Tamai M. Sato H, et al. Among authors: wada y. Am J Ophthalmol. 2005 Sep;140(3):537-40. doi: 10.1016/j.ajo.2005.02.050. Am J Ophthalmol. 2005. PMID: 16139010

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

3,658 results

Search Page