Seishima M - Search Results

1

Characterization of melanosomes and melanin in Japanese patients with Hermansky-Pudlak syndrome types 1, 4, 6, and 9.

Okamura K, Abe Y, Araki Y, Wakamatsu K, Seishima M, Umetsu T, Kato A, Kawaguchi M, Hayashi M, Hozumi Y, Suzuki T. Okamura K, et al. Among authors: seishima m. Pigment Cell Melanoma Res. 2018 Mar;31(2):267-276. doi: 10.1111/pcmr.12662. Epub 2017 Nov 2. Pigment Cell Melanoma Res. 2018. PMID: 29054114

2

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

Okamura K, Abe Y, Fukai K, Tsuruta D, Suga Y, Nakamura M, Funasaka Y, Oka M, Suzuki N, Wataya-Kaneda M, Seishima M, Hozumi Y, Kawaguchi M, Suzuki T. Okamura K, et al. Among authors: seishima m. J Dermatol Sci. 2015 Jul;79(1):88-90. doi: 10.1016/j.jdermsci.2015.04.004. Epub 2015 Apr 28. J Dermatol Sci. 2015. PMID: 25982145 No abstract available.

3

Increased antibody levels to desmogleins 1 and 3 after administration of carbamazepine.

Yoshimura T, Seishima M, Nakashima K, Yasuhara Y, Adachi S, Kawaguchi M, Minoura N, Nakao T, Kobayashi J, Yamazaki F. Yoshimura T, et al. Among authors: seishima m. Clin Exp Dermatol. 2001 Jul;26(5):441-5. doi: 10.1046/j.1365-2230.2001.00854.x. Clin Exp Dermatol. 2001. PMID: 11488835

4

Characterization of NLRP3 variants in Japanese cryopyrin-associated periodic syndrome patients.

Ohnishi H, Teramoto T, Iwata H, Kato Z, Kimura T, Kubota K, Nishikomori R, Kaneko H, Seishima M, Kondo N. Ohnishi H, et al. Among authors: seishima m. J Clin Immunol. 2012 Apr;32(2):221-9. doi: 10.1007/s10875-011-9629-0. Epub 2011 Dec 24. J Clin Immunol. 2012. PMID: 22193915

5

A Japanese family case with juvenile onset Behçet's disease caused by TNFAIP3 mutation.

Ohnishi H, Kawamoto N, Seishima M, Ohara O, Fukao T. Ohnishi H, et al. Among authors: seishima m. Allergol Int. 2017 Jan;66(1):146-148. doi: 10.1016/j.alit.2016.06.006. Epub 2016 Jul 19. Allergol Int. 2017. PMID: 27451268 Free article. No abstract available.

6

Clinical correlations with dermatomyositis-specific autoantibodies in adult Japanese patients with dermatomyositis: a multicenter cross-sectional study.

Hamaguchi Y, Kuwana M, Hoshino K, Hasegawa M, Kaji K, Matsushita T, Komura K, Nakamura M, Kodera M, Suga N, Higashi A, Ogusu K, Tsutsui K, Furusaki A, Tanabe H, Sasaoka S, Muro Y, Yoshikawa M, Ishiguro N, Ayano M, Muroi E, Fujikawa K, Umeda Y, Kawase M, Mabuchi E, Asano Y, Sodemoto K, Seishima M, Yamada H, Sato S, Takehara K, Fujimoto M. Hamaguchi Y, et al. Among authors: seishima m. Arch Dermatol. 2011 Apr;147(4):391-8. doi: 10.1001/archdermatol.2011.52. Arch Dermatol. 2011. PMID: 21482889

7

A novel TRPS1 mutation in a family with tricho-rhino-phalangeal syndrome type 1.

Fujisawa T, Fukao T, Shimomura Y, Seishima M. Fujisawa T, et al. Among authors: seishima m. J Dermatol. 2014 Jun;41(6):514-7. doi: 10.1111/1346-8138.12511. J Dermatol. 2014. PMID: 24909213

8

Clinical evaluation of anti-aminoacyl tRNA synthetase antibodies in Japanese patients with dermatomyositis.

Matsushita T, Hasegawa M, Fujimoto M, Hamaguchi Y, Komura K, Hirano T, Horikawa M, Kondo M, Orito H, Kaji K, Saito Y, Matsushita Y, Kawara S, Yasui M, Seishima M, Ozaki S, Kuwana M, Ogawa F, Sato S, Takehara K. Matsushita T, et al. Among authors: seishima m. J Rheumatol. 2007 May;34(5):1012-8. Epub 2007 Feb 15. J Rheumatol. 2007. PMID: 17309126

9

Wells' syndrome associated with Trichophyton infection.

Hattori Y, Seishima M. Hattori Y, et al. Among authors: seishima m. J Dermatol. 2019 Dec;46(12):e451-e452. doi: 10.1111/1346-8138.15085. Epub 2019 Sep 9. J Dermatol. 2019. PMID: 31502286 No abstract available.

10

Multiple familial trichoepithelioma with a novel mutation of the CYLD gene.

Fujii A, Matsuyama K, Mizutani Y, Kanoh H, Nakano H, Seishima M. Fujii A, et al. Among authors: seishima m. J Dermatol. 2017 Sep;44(9):e228-e229. doi: 10.1111/1346-8138.13901. Epub 2017 May 10. J Dermatol. 2017. PMID: 28488373 No abstract available.

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