- 15.
- Hayashi M, Kawaguchi M, Hozumi Y, Nakano H, Sawamura D, Suzuki Tamio. Dystrophic epidermolysis bullosa pruriginosa of elderly onset.
J Dermatol 2011; 38(2): 173-178.10. - 14.
- Narumi H, Nakano H, Matsuzaki Y, Sawamura D, Hanada K. Immunohistochemical analysis of in vivo UVB-induced secretion of IL-1α and IL-6 in keratinocytes.
Mol Med Report. 2011; 4(4): 611-614. - 13.
- Koga H, Hamada T, Ishii N, Fukuda S, Sakaguchi S, Nakano H, Tamai K, Sawamura D, Hashimoto T. Exon 87 skipping of the COL7A1 gene in dominant dystrophic epidermolysis bullosa.
J Dermatol. 2011;38(5):489-492. - 12.
- Umegaki N, Nakano H, Tamai K, Mitsuhashi Y, Akasaka E, Sawamura D, Katayama I. Vörner type palmoplantar keratoderma: novel KRT9 mutation associated with knuckle pad-like lesions and recurrent mutation causing digital mutilation.
Br J Dermatol. 2011; 165(1): 199-201. - 11.
- Nakamura H, Natsuga K, Nishie W, McMillan JR, Nakamura H, Sawamura D, Akiyama M, Shimizu H. DNA-based prenatal diagnosis of plectin-deficient epidermolysis bullosa simplex associated with pyloric atresia.
Int J Dermatol. 2011;50(4):439-442.6. - 10.
- Matsuzaki Y, Rokunohe A, Nishikawa Y, Nakano H, Sawamura D. Actinic granuloma associated with erythema nodosum.
Eur J Dermatol. 2011 ;21(5):806-7.5. - 9.
- Ohashi M, Shu E, Nagai M, Murase K, Nakano H, Tamai K, Sawamura D, Hiroka T, Seishima M, Kitajima Y, Aoyama Y. Two cases of recessive dystrophic epidermolysis bullosa diagnosed as severe generalized.
J Dermatol 2011; 38(9): 893-899. - 8.
- Murase K, Kanoh H, Ishii N, Hashimoto T, Nakano H, Sawamura D, Seishima M. Bullous dermolysis of the newborn and dystrophic epidermolysis bullosa pruriginosa within the same family: two phenotypes associated with a COL7A1 mutation.
Acta Derm Venereol. 2011; 91(6): 730-1. - 7.
- Frew J, Lim SW, Klausseger A, Chow CW, Tran K, Su J, Orchard D, Varigos G, Sawamura D, Nishie W, Shimizu H, Murrell DF. Autosomal dominant bullous dermolysis of the newborn associated with a heterozygous missense mutation p.G1673R in type VII collagen.
Australas J Dermatol. 2011; 52(4): e1-4.2. - 6.
- Narumi H, Nakano H, Matsuzaki Y, Sawamura D, Hanada K. Immunohistochemical analysis of in vivo UVB-induced secretion of IL-1 and IL-6 in keratinocytes.
Mol Med Report. 2011, in press. - 5.
- Takeda H, Nakajima K, Kaneko T, Harada K, Matsuzaki Y, Sawamura D. Follicular mucinosis associated with radiation therapy.
J Dermatol. 2011; 38(11): 1116-1118. - 4.
- Akasaka E, Nakano H, Nakano A, Toyomaki Y, Takiyoshi N, Rokunohe D, Nishikawa Y, Korekawa A, Matsuzaki Y, Mitsuhashi Y, Sawamura D. Diffuse and focal palmoplantar keratoderma can be caused by a keratin 6c mutation.
Br J Dermatol. 2011 ;165(6):1290-2. - 3.
- Korewawa A, Nakano H, Rokunohe D, Akasaka E, Nakajima K, Toyomaki Y, Sawamura D. Buschke-Ollendorff syndrome pathogenetic mutation in an Intron/Exon boundary of the LEMD3 gene.
Hirosaki Med J. 62, 117-121, 2011. - 2.
- Ikenaka S, Aizu T, Kambe Y, Yamazaki T, Nakano H, Hanada K, Sawamura D, Tsuchida S. Expression of raf kinase inhibitor protein in keratinocyte differentiation in the mouse epidermis.
Hirosaki Med J. 62, 166-172, 2011. - 1.
- Akasaka E, Nakano H, Jin K, Kimura K, Rokunohe D, Imokawa G, Sawamura D. The Interaction of photo protective effects between keratinocytes and melanocytes via endothelin-1/stem cell factor signaling.
Hirosaki Med J, 62, 138-143, 2011.
