Tomita Y - Search Results

1

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: tomita y. 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.

2

Six novel P gene mutations and oculocutaneous albinism type 2 frequency in Japanese albino patients.

Suzuki T, Miyamura Y, Matsunaga J, Shimizu H, Kawachi Y, Ohyama N, Ishikawa O, Ishikawa T, Terao H, Tomita Y. Suzuki T, et al. Among authors: tomita y. J Invest Dermatol. 2003 May;120(5):781-3. doi: 10.1046/j.1523-1747.2003.12127.x. J Invest Dermatol. 2003. PMID: 12713581 Free article.

3

Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria.

Miyamura Y, Suzuki T, Kono M, Inagaki K, Ito S, Suzuki N, Tomita Y. Miyamura Y, et al. Among authors: tomita y. Am J Hum Genet. 2003 Sep;73(3):693-9. doi: 10.1086/378209. Epub 2003 Aug 11. Am J Hum Genet. 2003. PMID: 12916015 Free PMC article.

4

A patient with subclinical oculocutaneous albinism type 2 diagnosed on getting severely sunburned.

Kawai M, Suzuki T, Ito S, Inagaki K, Suzuki N, Tomita Y. Kawai M, et al. Among authors: tomita y. Dermatology. 2005;210(4):322-3. doi: 10.1159/000084758. Dermatology. 2005. PMID: 15942220

5

High frequency of Hermansky-Pudlak syndrome type 1 (HPS1) among Japanese albinism patients and functional analysis of HPS1 mutant protein.

Ito S, Suzuki T, Inagaki K, Suzuki N, Takamori K, Yamada T, Nakazawa M, Hatano M, Takiwaki H, Kakuta Y, Spritz RA, Tomita Y. Ito S, et al. Among authors: tomita y. J Invest Dermatol. 2005 Oct;125(4):715-20. doi: 10.1111/j.0022-202X.2005.23884.x. J Invest Dermatol. 2005. PMID: 16185271 Free article.

6

Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family with ADAR1 mutation.

Tojo K, Sekijima Y, Suzuki T, Suzuki N, Tomita Y, Yoshida K, Hashimoto T, Ikeda S. Tojo K, et al. Among authors: tomita y. Mov Disord. 2006 Sep;21(9):1510-3. doi: 10.1002/mds.21011. Mov Disord. 2006. PMID: 16817193

7

Ten novel mutations of the ADAR1 gene in Japanese patients with dyschromatosis symmetrica hereditaria.

Suzuki N, Suzuki T, Inagaki K, Ito S, Kono M, Horikawa T, Fujiwara S, Ishiko A, Matsunaga K, Aoyama Y, Tosaki-Ichikawa H, Tomita Y. Suzuki N, et al. Among authors: tomita y. J Invest Dermatol. 2007 Feb;127(2):309-11. doi: 10.1038/sj.jid.5700528. Epub 2006 Aug 17. J Invest Dermatol. 2007. PMID: 16917490 Free article.

8

Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria: histological observation and comparison of genotypes and clinical phenotypes.

Kondo T, Suzuki T, Mitsuhashi Y, Ito S, Kono M, Komine M, Akita H, Tomita Y. Kondo T, et al. Among authors: tomita y. J Dermatol. 2008 Jul;35(7):395-406. doi: 10.1111/j.1346-8138.2008.00493.x. J Dermatol. 2008. PMID: 18705826

9

Dyschromatosis symmetrica hereditaria associated with neurological disorders.

Kondo T, Suzuki T, Ito S, Kono M, Negoro T, Tomita Y. Kondo T, et al. Among authors: tomita y. J Dermatol. 2008 Oct;35(10):662-6. doi: 10.1111/j.1346-8138.2008.00540.x. J Dermatol. 2008. PMID: 19017046

10

Dyschromatosis symmetrica hereditaria by ADAR1 mutations and viral encephalitis: a hidden link?

Kono M, Akiyama M, Suganuma M, Tomita Y, Sanchez-Valle A. Kono M, et al. Among authors: tomita y. Int J Dermatol. 2013 Dec;52(12):1582-4. doi: 10.1111/j.1365-4632.2011.05372.x. Int J Dermatol. 2013. PMID: 24261734 No abstract available.

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