• 2243 Citations
  • 25 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
Dermatomyositis Medicine & Life Sciences
Skin Medicine & Life Sciences
DNA Mutational Analysis Medicine & Life Sciences
Antibodies Medicine & Life Sciences
Keratinocytes Medicine & Life Sciences

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Research Output 1997 2019

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., 01-03-2019, In : International Journal of Dermatology. 58, 3, p. 350-353 4 p.

Research output: Contribution to journalArticle

Postpartum Period

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

Gastrointestinal bleeding with severe mucosal involvement in a patient with generalized pustular psoriasis without IL36RN mutation

Komatsuda, S., Kamata, M., Chijiwa, C., Namiki, K., Fukaya, S., Hayashi, K., Fukuyasu, A., Tanaka, T., Ishikawa, T., Ohnishi, T., Abe, K., Yamamoto, T., Aozasa, N., Sugiura, K. & Tada, Y., 01-01-2019, In : Journal of Dermatology. 46, 1, p. 73-75 3 p.

Research output: Contribution to journalArticle


Generalized pustular psoriasis from heterozygous IL36RN mutation developed after liver surgery

Fukushima, H., Iwata, Y., Numata, S., Saito, K., Watanabe, S., Kobayashi, T. & Sugiura, K., 01-01-2019, In : Journal of Dermatology.

Research output: Contribution to journalLetter

1 Citation (Scopus)

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