• 2160 Citations
  • 24 h-Index
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Fingerprint Fingerprint is based on mining the text of the person's scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

Mutation Medicine & Life Sciences
Autoantibodies Medicine & Life Sciences
Psoriasis Medicine & Life Sciences
Skin Medicine & Life Sciences
Dermatomyositis Medicine & Life Sciences
DNA Mutational Analysis Medicine & Life Sciences
Antibodies Medicine & Life Sciences
Lamellar Ichthyosis Medicine & Life Sciences

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Research Output 1997 2019

CXCL12 regulates differentiation of human immature melanocyte precursors as well as their migration

Yamada, T., Hasegawa, S., Hasebe, Y., Kawagishi-Hotta, M., Arima, M., Iwata, Y., Kobayashi, T., Numata, S., Yamamoto, N., Nakata, S., Sugiura, K. & Akamatsu, H., 22-01-2019, In : Archives of Dermatological Research. 311, 1, p. 55-62 8 p.

Research output: Contribution to journalArticle

Stem Cells
Hair Follicle
Hair Color

An effective and promising treatment with adalimumab for impetigo herpetiformis with postpartum flare-up

Yamashita, T., Hamada, T., Maruta, Y., Kajita, A., Hirai, Y., Morizane, S., Watanabe, S., Sugiura, K. & Iwatsuki, K., 01-01-2018, (Accepted/In press) In : International Journal of Dermatology. 58, 3, p. 350-353 4 p.

Research output: Contribution to journalArticle

Postpartum Period
1 Citations

A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi–Goutières and Singleton–Merten syndromes in a single patient

Takeichi, T., Katayama, C., Tanaka, T., Okuno, Y., Murakami, N., Kono, M., Sugiura, K., Aoyama, Y. & Akiyama, M., 01-02-2018, In : British Journal of Dermatology. 178, 2, p. e111-e113

Research output: Contribution to journalLetter

Singleton Merten syndrome
4 Citations

Autoinflammatory keratinization diseases: An emerging concept encompassing various inflammatory keratinization disorders of the skin

Akiyama, M., Takeichi, T., McGrath, J. A. & Sugiura, K., 01-05-2018, In : Journal of Dermatological Science. 90, 2, p. 105-111 7 p.

Research output: Contribution to journalReview article

Skin Diseases

Autosomal dominant progressive hyperpigmentation and lentigines in a Japanese pedigree due to a missense mutation near the C-terminus of KIT

Takeichi, T., Sugiura, K., Tanahashi, K., Noda, K., Kono, M. & Akiyama, M., 01-11-2018, In : British Journal of Dermatology. 179, 5, p. 1210-1211 2 p.

Research output: Contribution to journalLetter

Missense Mutation