Komine M - Search Results

1

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: komine m. J Dermatol. 2008 Jul;35(7):395-406. doi: 10.1111/j.1346-8138.2008.00493.x. J Dermatol. 2008. PMID: 18705826

2

Linear and whorled naevoid hypermelanosis: a case with systemic involvement and trisomy 18 mosaicism.

Komine M, Hino M, Shiina M, Kanazawa I, Soma Y, Tamaki K. Komine M, et al. Br J Dermatol. 2002 Mar;146(3):500-2. doi: 10.1046/j.1365-2133.2002.04532.x. Br J Dermatol. 2002. PMID: 11952553 Review.

3

Does Hermansky-Pudlak syndrome predispose to systemic lupus erythematosus?

Mitsui H, Komine M, Watanabe T, Kikuchi K, Okochi H, Tamaki K. Mitsui H, et al. Among authors: komine m. Br J Dermatol. 2002 May;146(5):908-11. doi: 10.1046/j.1365-2133.2002.04670.x. Br J Dermatol. 2002. PMID: 12000395

4

A keratin 9 Gene mutation (Asn160Ser) in a Japanese patient with epidermolytic palmoplantar keratoderma.

Tsunemi Y, Hattori N, Saeki H, Adachi M, Komine M, Nakagawa H, Tamaki K. Tsunemi Y, et al. Among authors: komine m. J Dermatol. 2002 Dec;29(12):768-72. doi: 10.1111/j.1346-8138.2002.tb00220.x. J Dermatol. 2002. PMID: 12532041

5

Novel mutation (Asp158Val) in H1 domain of keratin 5 gene in a Japanese patient with Köbner-type epidermolysis bullosa simplex.

Saeki H, Nakamura K, Tsunemi Y, Komine M, Tamaki K. Saeki H, et al. Among authors: komine m. J Dermatol. 2006 Oct;33(10):692-5. doi: 10.1111/j.1346-8138.2006.00160.x. J Dermatol. 2006. PMID: 17040498

6

Serum 5-S-cysteinyldopa levels in patients with psoriasis undergoing narrowband ultraviolet B phototherapy.

Kikuchi K, Wakamatsu K, Tada Y, Komine M, Ito S, Tamaki K. Kikuchi K, et al. Among authors: komine m. Clin Exp Dermatol. 2008 Nov;33(6):750-3. doi: 10.1111/j.1365-2230.2008.02792.x. Clin Exp Dermatol. 2008. PMID: 18954414

7

Duration of remission period of narrowband ultraviolet B therapy on psoriasis vulgaris.

Karakawa M, Komine M, Takekoshi T, Sakurai N, Minatani Y, Tada Y, Saeki H, Tamaki K. Karakawa M, et al. Among authors: komine m. J Dermatol. 2011 Jul;38(7):655-60. doi: 10.1111/j.1346-8138.2010.01053.x. Epub 2010 Oct 6. J Dermatol. 2011. PMID: 21352300

8

Skipped exon in COL7A1 determines the clinical phenotypes of dystrophic epidermolysis bullosa.

Toyonaga E, Nishie W, Komine M, Murata S, Shinkuma S, Natsuga K, Nakamura H, Ohtsuki M, Shimizu H. Toyonaga E, et al. Among authors: komine m. Br J Dermatol. 2015 Apr;172(4):1141-4. doi: 10.1111/bjd.13386. Epub 2015 Feb 25. Br J Dermatol. 2015. PMID: 25196227 No abstract available.

9

Case of H syndrome with massive skin involvement, retroperitoneal fibrosis and Raynaud's phenomenon with a novel mutation in the SLC29A3 gene.

Fujita E, Komine M, Tsuda H, Adachi A, Murata S, Kamata Y, Minota S, Ohtsuki M. Fujita E, et al. Among authors: komine m. J Dermatol. 2015 Dec;42(12):1169-71. doi: 10.1111/1346-8138.12973. Epub 2015 Jun 13. J Dermatol. 2015. PMID: 26074390

10

Systemic lupus erythematosus with hereditary deficiency of the fourth component of complement.

Komine M, Matsuyama T, Nojima Y, Minoda S, Furue M, Tsuchida T, Sakai S, Ishibashi Y. Komine M, et al. Int J Dermatol. 1992 Sep;31(9):653-6. doi: 10.1111/j.1365-4362.1992.tb03989.x. Int J Dermatol. 1992. PMID: 1459767 No abstract available.

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