- 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.
- 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.
- 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.
- 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]
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
