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Association Study of ARMC9 Gene Variants with Vogt-Koyanagi-Harada Disease in Japanese Patients.
Ohno T, Meguro A, Takeuchi M, Yamane T, Teshigawara T, Kitaichi N, Horie Y, Namba K, Ohno S, Nakao K, Sakamoto T, Sakai T, Nakano T, Keino H, Okada AA, Takeda A, Fukuhara T, Mashimo H, Ohguro N, Oono S, Enaida H, Okinami S, Mizuki N. Ohno T, et al. Among authors: okinami s. Ocul Immunol Inflamm. 2019;27(5):699-705. doi: 10.1080/09273948.2018.1523438. Epub 2018 Nov 5. Ocul Immunol Inflamm. 2019. PMID: 30395750
Investigation of the association between IL10 gene polymorphisms and Vogt-Koyanagi-Harada disease in a Japanese population.
Higashi K, Meguro A, Takeuchi M, Yamane T, Kitaichi N, Horie Y, Namba K, Ohno S, Nakao K, Sakamoto T, Sakai T, Tsuneoka H, Keino H, Okada AA, Takeda A, Fukuhara T, Mashimo H, Ohguro N, Oono S, Enaida H, Okinami S, Mizuki N. Higashi K, et al. Among authors: okinami s. Ophthalmic Genet. 2017 Mar-Apr;38(2):187-189. doi: 10.3109/13816810.2016.1145698. Epub 2016 Apr 4. Ophthalmic Genet. 2017. PMID: 27046676 No abstract available.
Variants in IL23R-C1orf141 and ADO-ZNF365-EGR2 are associated with susceptibility to Vogt-Koyanagi-Harada disease in Japanese population.
Sakono T, Meguro A, Takeuchi M, Yamane T, Teshigawara T, Kitaichi N, Horie Y, Namba K, Ohno S, Nakao K, Sakamoto T, Sakai T, Nakano T, Keino H, Okada AA, Takeda A, Ito T, Mashimo H, Ohguro N, Oono S, Enaida H, Okinami S, Horita N, Ota M, Mizuki N. Sakono T, et al. Among authors: okinami s. PLoS One. 2020 May 21;15(5):e0233464. doi: 10.1371/journal.pone.0233464. eCollection 2020. PLoS One. 2020. PMID: 32437414 Free PMC article.
Ocular manifestations in adult T-cell leukemia/lymphoma.
Shibata K, Shimamoto Y, Nishimura T, Okinami S, Yamada H, Miyahara M. Shibata K, et al. Among authors: okinami s. Ann Hematol. 1997 Apr;74(4):163-8. doi: 10.1007/s002770050276. Ann Hematol. 1997. PMID: 9174543
105 results