Suzuki T - Search Results

1

Generalized vitiligo and associated autoimmune diseases in Japanese patients and their families.

Narita T, Oiso N, Fukai K, Kabashima K, Kawada A, Suzuki T. Narita T, et al. Among authors: suzuki t. Allergol Int. 2011 Dec;60(4):505-8. doi: 10.2332/allergolint.11-OA-0303. Epub 2011 Jul 25. Allergol Int. 2011. PMID: 21778811 Free article.

2

Analysis of KIT, SCF, and initial screening of SLUG in patients with piebaldism.

Murakami T, Hosomi N, Oiso N, Giovannucci-Uzielli ML, Aquaron R, Mizoguchi M, Kato A, Ishii M, Bitner-Glindzicz M, Barnicoat A, Wilson L, Tsukamoto K, Ueda H, Mancini AJ, Suzuki T, Riley J, Miertus J, Camargo M, Santoro-Zea A, Atkin J, Fukai K. Murakami T, et al. Among authors: suzuki t. J Invest Dermatol. 2005 Mar;124(3):670-2. doi: 10.1111/j.0022-202X.2005.23637.x. J Invest Dermatol. 2005. PMID: 15737214 Free article. No abstract available.

3

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: suzuki t. 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.

4

OCA4: evidence for a founder effect for the p.D157N mutation of the MATP gene in Japanese and Korean.

Inagaki K, Suzuki T, Ito S, Suzuki N, Fukai K, Horiuchi T, Tanaka T, Manabe E, Tomita Y. Inagaki K, et al. Among authors: suzuki n, suzuki t. Pigment Cell Res. 2005 Oct;18(5):385-8. doi: 10.1111/j.1600-0749.2005.00261.x. Pigment Cell Res. 2005. PMID: 16162179

5

Mutation analyses of patients with dyschromatosis symmetrica hereditaria: five novel mutations of the ADAR1 gene.

Murata I, Hayashi M, Hozumi Y, Fujii K, Mitsuhashi Y, Oiso N, Fukai K, Kuroki N, Mori Y, Utani A, Tomita Y, Fujita Y, Suzuki T. Murata I, et al. Among authors: suzuki t. J Dermatol Sci. 2010 Jun;58(3):218-20. doi: 10.1016/j.jdermsci.2010.04.001. Epub 2010 Apr 14. J Dermatol Sci. 2010. PMID: 20439151 No abstract available.

6

Dermoscopic features in a case of dyschromatosis symmetrica hereditaria.

Oiso N, Murata I, Hayashi M, Amatsu A, Yoshida M, Suzuki T, Kawada A. Oiso N, et al. Among authors: suzuki t. J Dermatol. 2011 Jan;38(1):91-3. doi: 10.1111/j.1346-8138.2010.01110.x. Epub 2010 Nov 26. J Dermatol. 2011. PMID: 21175763 No abstract available.

7

Two children with a mild or moderate piebaldism phenotype and a father without leukoderma in a family with the same recurrent missense mutation in the kinase domain of KIT.

Narita T, Oiso N, Fukai K, Motokawa T, Hayashi M, Yokoyama K, Hozumi Y, Kawada A, Suzuki T. Narita T, et al. Among authors: suzuki t. Eur J Dermatol. 2011 May-Jun;21(3):446-7. doi: 10.1684/ejd.2011.1350. Eur J Dermatol. 2011. PMID: 21680281 No abstract available.

8

Nonsegmental vitiligo and autoimmune mechanism.

Oiso N, Suzuki T, Fukai K, Katayama I, Kawada A. Oiso N, et al. Among authors: suzuki t. Dermatol Res Pract. 2011;2011:518090. doi: 10.1155/2011/518090. Epub 2011 Jul 26. Dermatol Res Pract. 2011. PMID: 21804820 Free PMC article.

9

Repigmentation of leukoderma in a piebald patient associated with a novel c-KIT gene mutation, G592E, of the tyrosine kinase domain.

Arase N, Wataya-Kaneda M, Oiso N, Tanemura A, Kawada A, Suzuki T, Katayama I. Arase N, et al. Among authors: suzuki t. J Dermatol Sci. 2011 Nov;64(2):147-9. doi: 10.1016/j.jdermsci.2011.08.006. Epub 2011 Aug 27. J Dermatol Sci. 2011. PMID: 21925843 No abstract available.

10

Blaschkitis-like eruptions with hypodontia and low IκB kinase gamma expression.

Oiso N, Kimura M, Tanemura A, Tsuruta D, Itou T, Suzuki T, Katayama I, Kawada A. Oiso N, et al. Among authors: suzuki t. J Dermatol. 2012 Nov;39(11):941-3. doi: 10.1111/j.1346-8138.2011.01493.x. Epub 2012 Feb 2. J Dermatol. 2012. PMID: 22300171 No abstract available.

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