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Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis.
Suzuki N, Suzuki T, Inagaki K, Ito S, Kono M, Fukai K, Takama H, Sato K, Ishikawa O, Abe M, Shimizu H, Kawai M, Horikawa T, Yoshida K, Matsumoto K, Terui T, Tsujioka K, Tomita Y. Suzuki N, et al. Among authors: takama h. J Invest Dermatol. 2005 Jun;124(6):1186-92. doi: 10.1111/j.0022-202X.2005.23732.x. J Invest Dermatol. 2005. PMID: 15955093 Free article.
Unilateral generalized linear porokeratosis with nail dystrophy.
Kono M, Yokoyama N, Ogawa Y, Takama H, Sugiura K, Akiyama M. Kono M, et al. Among authors: takama h. J Dermatol. 2016 Mar;43(3):286-7. doi: 10.1111/1346-8138.13204. Epub 2015 Nov 21. J Dermatol. 2016. PMID: 26589366 No abstract available.
Unilateral case of multiple minute digitate hyperkeratosis.
Okochi S, Kono M, Takama H, Takeichi T, Muro Y, Akiyama M. Okochi S, et al. Among authors: takama h. J Dermatol. 2019 Jun;46(6):e210-e211. doi: 10.1111/1346-8138.14777. Epub 2019 Jan 28. J Dermatol. 2019. PMID: 30690772 No abstract available.
Novel and recurrent ATP2A2 mutations in Japanese patients with Darier's disease.
Noda K, Takeichi T, Okuno Y, Takama H, Miura S, Kagami S, Hino H, Nakamura Y, Fujio Y, Konohana I, Otani A, Mukai H, Sugiura K, Akiyama M. Noda K, et al. Among authors: takama h. Nagoya J Med Sci. 2016 Dec;78(4):485-492. doi: 10.18999/nagjms.78.4.485. Nagoya J Med Sci. 2016. PMID: 28008204 Free PMC article.
80 results