2019年(業績・論文)

  1. Saito A, Okiyama N, Inoue S, Kubota N, Nakamura Y, Ishitsuka Y, Watanabe R, Nakano H, Fujisawa Y. Novel mutation of the ferrochelatase gene in a Japanese family with erythropoietic protoporphyria. J Dermatol. 2020 Apr;47(4):e114-e116. doi: 10.1111/1346-8138.15258. Epub 2020 Feb 13.
  2. Kudo M, Ishiura N, Tamura-Nakano M, Shimizu T, Kamata M, Akasaka E, Nakano H, Okuma Y, Tada Y, Okochi H, Tamaki T. Abnormal keratinization and cutaneous inflammation in Mal de Meleda. J Dermatol. 2020 May;47(5):554-558. doi: 10.1111/1346-8138.15296. Epub 2020 Mar 10.
  3. Maruyama A, Wada M, Kondo Y, Kira M, Nakano H, Katoh N. Case of bullous pemphigoid following Hailey-Hailey disease with novel mutation of the ATP2C1 gene. J Dermatol. 2020 Mar;47(3):e79-e80.
  4. Takahashi M, Matsuzaki Y, Nakano H, Sawamura D. Partial spontaneous regression of pediatric large fibroblastic connective tissue nevus. J Dermatol. 2020 Mar 18. doi: 10.1111/1346-8138.15320. [Epub ahead of print]
  5. Saito A, Okiyama N, Inoue S, Kubota N, Nakamura Y, Ishitsuka Y, Watanabe R, Nakano H, Fujisawa Y. Novel mutation of the ferrochelatase gene in a Japanese family with erythropoietic protoporphyria. J Dermatol. 2020 Apr;47(4):e114-e116. doi: 10.1111/1346-8138.15258. Epub 2020 Feb 13.
  6. Higuchi S, Nishida M, Fukai K, Nakano H, Yorifuji T. Acrodermatitis enteropathica: a hereditary form of zinc deficiency. QJM. 2020 May 22:hcaa176. doi: 10.1093/qjmed/hcaa176. Online ahead of print.
  7. Hayashi M, Nakano H, Sawamura D, Suzuki T. Japanese case of Papillon-Lefèvre syndrome with novel compound heterozygous mutations. J Dermatol. 2020 Aug;47(8):e293-e295. doi: 10.1111/1346-8138.15412. Epub 2020 May 28.
  8. Korekawa A, Nakajima K, Nakano H, Sawamura D. Benign neonatal hemangiomatosis with early regression of skin lesions: A case report and review of the published work J Dermatol. 2020 Aug;47(8):911-916. doi: 10.1111/1346-8138.15413. Epub 2020 Jun 3.
  9. Fukui T, Akasaka E, Rokunohe D, Matsuzaki Y, Sawamura D, Kabashima K, Nakano H. Analysis of the mechanism underlying a mild phenotype of hereditary coproporphyria due to a homozygous missense mutation in the transcription initiation codon of the coproporphyrinogen III oxidase gene. J Dermatol Sci. 2020 Jun 15:S0923-1811(20)30202-4. doi: 10.1016/j.jdermsci.2020.06.006. Online ahead of print.
  10. Kariya H, Nakano H, Ishii N, Kaimi Y, Imai K, Nakanishi Y, Kunihiro N, Fukai K. Crouzon syndrome with acanthosis nigricans and prominent diffuse hyperpigmentation associated with gain-of-function A391E mutation in FGFR3 gene. J Dermatol. 2020 Dec;47(12):e451-e452. doi: 10.1111/1346-8138.15580. Epub 2020 Aug 29.
  11. Makita E, Matsuzaki Y, Fukui T, Matsui A, Minakawa S, Nakano H, Ito K, Kijima H, Sawamura D. Autoantibodies to BPAG1e Trigger Experimental Bullous Pemphigoid in Mice. J Invest Dermatol. 2020 Oct 16:S0022-202X(20)32173-4. doi: 10.1016/j.jid.2020.08.031. Online ahead of print.
  12. Kawakami T, Akiyama M, Ishida-Yamamoto A, Nakano H, Mitoma C, Yoneda K, Suga Y. Clinical practice guide for the treatment of perforating dermatosis. J Dermatol. 2020 Dec;47(12):1374-1382. doi: 10.1111/1346-8138.15647. Epub 2020 Oct 23.
  13. Nakai I, Nakai K, Teramae A, Fukai K, Nakano H, Tsuruta D. Novel ATP2C1 frame-shift mutation in a mild case of early onset sporadic Hailey-Hailey disease. J Dermatol. 2020 Nov 8. doi: 10.1111/1346-8138.15689. Online ahead of print.

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