2018年の業績を追加しました。

2018年の業績を追加しました。

Ohyama A, Nakano H, Imanishi Y, Seto T, Tsuruta, Kousinn D, Fukai K. A novel missense mutation of the STS gene in two siblings with X-linked ichthyosis, complicated by short stature, bone density reduction, epilepsy, and cryptorchidism.
Clin Exp Dermatol 2018 in press.

2018年の業績を追加しました。

2018年の業績を追加しました。

Korekawa A, Kaneko T, Nakano H, Sawamura D. Pyogenic granuloma-like Kaposi’s sarcoma on the first toe.
J Dermatol. 2018 in press.

Komori T, Dainichi T, Otsuka A, Nakano H, Sawamura D, Ishida-Yamamoto A, and Kabashima K. Mild dystrophic epidermolysis bullosa associated with homozygous gene mutation c.6216+5G>T in type VII collagen ultrastrucrurally suggestive of the decreased number of anchoring fibrils.
J Dermatol, 2018 in press.

Hattori M, Ishikawa O, Oikawa D, Amano H, Yasuda M, Kaira K, Ishida-Yamamoto A, Nakano H, Sawamura D, Terawaki S, Wakamatsu K, Tokunaga F, Shimizu A. In-frame Val216 -Ser217 deletion of KIT in mild piebaldism causes aberrant secretion and SCF response.
J Dermatol Sci 2018, in press.

2018年の業績を追加しました。

2018年の業績を追加しました。

1. Komori T, Dainichi T, Masuno Y, Otsuka A, Nakano H, Sawamura D, Ishida-Yamamoto A, and Kabashima K. The p.Glu477Lys mutation in Keratin 5 is not necessarily mortal in generalized severe epidermolysis bullosa simplex under intensive dressing care.
J Dermatol., in press.