12.Matsui A, Akasaka E, Rokunohe D, Matsuzaki Y, Sawamura D, Nakano H.The first Japanese case of familial porphyria cutanea tarda diagnosed by a UROD mutation.
J Dermatol Sci. 2019 Jan;93(1):65-67.

2019_JDS(93)_Matsui

11.Morimoto N, Shimizu A, Hattori M, Kuriyama Y, Nakano H, Ohnishi K. Dystrophic epidermolysis bullosa pruriginosa presenting with flagellate scarring lesions. Clin Exp Derm 2019; 44: e5-6.

10.Matsuzaki Y, Takahashi M, Minakawa S, Jin K, Nakano H, Sawamura D.Cutaneous collagenous vasculopathy induced by the vascular endothelial growth factorreceptor inhibitor axitinib.Int J Dermatol. 2018 Dec;57(12):e167-e169.

9. Morimoto N, Shimizu A, Hattori M, Kuriyama Y, Nakano H, Ohnishi K. Dystrophic epidermolysis bullosa pruriginosa with a flagellate scarring lesion.
Clin Exp Dermatol 2018, in press.

8. Yaginuma A, Itoh M, Akasaka E, Nakano H, Sawamura D, Nakagawa H, Asahina A. Novel mutation c.263A>G in the ACVRL1 gene in a Japanese patient with hereditary hemorrhagic telangiectasia 2.
J Dermatol 2018, in press.

7. Li  M, Nakano H, Higashi N, Saeki H. Incontinentia pigmenti in a Japanese newborn female with a novel frameshift mutation in the IKBKG gene.
J Dermatol, 2018 in press.

6. 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.

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

4. 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.

3. 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.

2. Hattori M, Shimizu A, Nakano H, Ishikawa O.
Mild phenotype of junctional epidermolysis bullosa with pyloric atresia due to a novel mutation of the ITGB4 gene.
J Dermatol, 2018 in press.

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, 2018 in press.