10.　Cho JW, Ryu HW, Kim SA, Nakano H, Lee KS. Weber-Cockayne Type Epidermolysis Bullosa Simplex Resulting from a Novel Mutation (c. 608T>C) in the Keratin 5 Gene.
Ann Dermatol. 2014 Dec;26(6):739-742.

9.　Yoshihara N, Nakano H, Sawamura D, Ikeda S. Novel missense mutation of COL7A1 in a recessive dystrophic epidermolysis bullosa patient with mild clinical phenotype.
J Dermatol. 2014; 41(10): 939-940.

9.　Park K, Nakano H, Sawamura D, Kabashima K, Miyachi Y. A case of dominant dystrophic epidermolysis bullosa with diabetes mellitus presenting as progressive recalcitrant blisters and erosions.
Int Wound J. 2014; 11(5): 567-568.

8.　Yasudo H, Ando T, Takeuchi M, Nakano H, Itonaga T, Takehara H, Isojima T, Miura K, Harita Y, Takita J, Oka A. Systemic lupus erythematosus complicated with liver cirrhosis in a patient with Papillon-Lefèvre syndrome.
Lupus. 2014; 23(14): 1523-1527.

7.　Minakawa S, Kaneko T, Rokunohe D, Nakajima K, Matsuzaki Y,
Nakano H, Hashimoto T, Sawamura D. Pemphigoid gestationis with prepartum flare.
J Dermatol. 2014; 41(9): 850-851.

6.　Kitazawa T, Kawakami T, Matsuoka M, Kimura S, Soma Y, Nakano H. Splicing mutation in the COL7A1 gene mRNA exon 71 in a female patient with pretibial epidermolysis bullosa.
J Dermatol. 2014; 41(11): 1018-1019.

5.　Inaba Y, Kanazawa N, Furukawa F, Sakurane Y, Nakano H, Sawamura D, Yoneda K, Hamada T, Hashimoto T.              Pachyonychia congenita in Japan: report of familial cases with a recurrent KRT16 mutation.
Eur J Dermatol 2014; 24(1): 122-123.

4.　Moritsugu R, Tamai K, Nakano H, Aizu T, Nakajima K, Yamazaki T, Sawamura D. Functional analysis of the nuclear localization signal of the POU transcription factor Skn‑1a in epidermal keratinocytes. Int J Mol Med 2014; 34(2): 539-44.

3.　Shinkuma S, Sawamura D, Fujita Y, Kawasaki H, Nakamura H, Inoie M, Nishie W, Shimizu H. Long-term Follow-up of Cultured Epidermal Autograft in a Patient with Recessive Dystrophic Epidermolysis Bullosa.
Acta Derm Venereol 2014; 94(1): 98-99.

2.　Ohashi M, Moriya C, Tanahashi K, Nakano H, Sawamura D, Seishima M . A new EDA gene mutation in a family of X-linked hypohidrotic ectodermal dysplasia.
J Dermatol Sci 2014 ; 74(2): 175-177.

1.　Mori N, Mizawa M, Hara H, Norisugi O, Makino T, Nakano H, Sawamura D, Shimizu T. Hailey-Hailey disease diagnosed based on an exacerbation of contact dermatitis with topical crotamiton.
Eur J Dermatol 2014 ;24(2):263-264.