- 18.
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Nishizawa A, Satoh T, Watanabe R, Takayama K, Nakano H, Sawamura D, Yokozeki H. Cowden syndrome: a novel mutation and overlooked glycogenic acanthosis in gingiva.
Br J Dermatol 2009; 160(5): 1116-1118. - 17.
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Matsui K, Makino T, Nakano H, Furuichi M, Sawamura D, Shimizu T: Squamous cell carcinoma arising from Darier’s disease.
Clin Exp Dermatol 2009; 34(8):1015-1016. - 16.
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Goto-Ohguchi Y, Nishie W, Akiyama M, Tateishi Y, Aoyagi S, Tsuji-Abe Y, Sawamura D, Ishii N, Hashimoto T, Shimizu H. A severe and refractory case of anti-p200 pemphigoid resulting in multiple skin ulcers and scar formation.
Dermatology 2009; 218(3): 265-271. - 15.
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Imada K, Dainichi T, Yokomizo A, Tsunoda T, Song YH, Nagasaki A, Sawamura D, Nishie W, Shimizu H, Fukagawa S, Urabe K, Furue M, Hashimoto T, Naito S.Birt-Hogg-Dub? syndrome with clear-cell and oncocytic renal tumour and trichoblastoma associated with a novel FLCN mutation.
Br J Dermatol 2009; 160(6): 1350-1353. - 14.
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Nishie W, Sawamura D, Natsuga K, Shinkuma S, Goto M, Shibaki A, Ujiie H, Olasz E, Yancey KB, Shimizu H. A novel humanized neonatal autoimmune blistering skin disease model induced by maternally transferred antibodies.
J Immunol 2009; 183(6): 4088-4093. - 13.
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Inokuma D, Sawamura D, Shibaki A, Abe R, Shimizu H. Scleroedema adultorum associated with sarcoidosis.
Clin Exp Dermatol 2009; 34(7): e428-429. - 12.
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Ito K, Sawamura D, Goto M, Nakamura H, Nishie W, Sakai K, Natsuga K, Shinkuma S, Shibaki A, Uitto J, Denton CP, Nakajima O, Akiyama M, Shimizu H. Keratinocyte-/Fibroblast-Targeted Rescue of Col7a1-Disrupted Mice and Generation of an Exact Dystrophic Epidermolysis Bullosa Model Using a Human COL7A1 Mutation.
Am J Pathol 2009; 175(6): 2508-2517. - 11.
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Hashikawa K, Hamada T, Ishii N, Fukuda S, Kuroki R, Nakama T, Yasumoto S, Tamai K, Nakano H, Sawamura D, Hashimoto T. The compound heterozygote for new/recurrent COL7A1 mutations in a Japanese patient with bullous dermolysis of the newborn.
J Dermatol Sci 2009; 56(1): 66-68. - 10.
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Amagai M, Ikeda S, Shimizu H, Iizuka H, Hanada K, Aiba S, Kaneko F, Izaki S, Tamaki K, Ikezawa Z, Takigawa M, Seishima M, Tanaka T, Miyachi Y, Katayama I, Horiguchi Y, Miyagawa S, Furukawa F, Iwatsuki K, Hide M, Tokura Y, Furue M, Hashimoto T, Ihn H, Fujiwara S, Nishikawa T, Ogawa H, Kitajima Y, Hashimoto K. A randomized double-blind trial of intravenous immunoglobulin for pemphigus.
J Am Acad Dermatol 2009; 60(4): 595-603. - 9.
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Oshima H, Matsuzaki Y, Takeuchi S, Nakano H, Sawamura D. CD20 positive primary cutaneous T-cell lymphoma presenting as a solitary extensive plaque.
Br J Dermatol 2009; 160(4): 894-896. - 8.
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Matsuzaki Y, Kimura K, Nakano H, Hanada K, Sawamura D. Localized pagetoid reticulosis (Woringer-Kolopp disease) in early childhood.
J Am Acad Dermatol 2009; 61(1): 120-123. - 7.
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Takiyoshi N, Nakano H, Rokunohe D, Akasaka E, Jin K, Aizu T, Kaneko T, Matsuzaki Y, Sawamura D, Ohara K. Eclipse in the subungual space: a diagnostic sign for subungual epidermal cyst?
Br J Dermatol 2009; 161(4): 962-963. - 6.
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Hamada T, Fukuda S, Ishii N, Abe T, Nagata K, Koro O, Hatano Y, Nakano H, Sawamura D, Hashimoto T. A Japanese family with dominant pretibial dystrophic epidermolysis bullosa: Identification of a new glycine substitution in the triple-helical collagenous domain of type VII collagen.
J Dermatol Sci 2009; 54(3): 212-214. - 5.
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Ochiai T, Nakano H, Rokunohe D, Akasaka E, Toyomaki Y, Mitsuhashi Y, Sawamura D. Novel p.M1T and recurrent p.G301S mutations in cathepsin C in a Japanese patient with Papillon-Lefevre syndrome: implications for understanding the genotype/phenotype relationship.
J Dermatol Sci 2009; 53(1): 73-75. - 4.
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Minakawa S, Nakano H, Takeda H, Mizukami H, Yagihashi S, Satou T, Sawamura D, Chromosome 22q11.2 deletion syndrome associated with severe eczema.
Clin Exp Dermatol 2009; 34(3): 410-411. - 3.
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Horie M, Nishio K, Fujita K, Endo S, Miyauchi A, Saito Y, Iwahashi H, Yamamoto K, Murayama H, Nakano H, Nanashima N, Niki E, Yoshida Y. Protein adsorption of ultrafine metal oxide and its influence on cytotoxicity toward cultured cell.
Chem Res Toxicol 2009; 22(3): 543-53. - 2.
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Takiyoshi N, Nakano H, Kaneko T, Aizu T, Nakajima K, Kimura K, Akasaka E, Rokunohe D, Nishizawa A, Kusumi T, Sawamura D. A linear basal cell carcinoma undergoing spontaneous regression.
Clin Exp Dermatol 2009; 34(7): e411-413. - 1.
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Nakano H, Nakamura Y, Kawamura T, Shibagaki N, Matsue H, Aizu T, Rokunohe Daiki, Akasaka E, Kimura K, Nishizawa A, Umegaki N, Mitsuhashi Y, Shimada S, Sawamura D. Novel and recurrent nonsense mutation of the SLC39A4 gene in Japanese patients with acrodermatitis enteropathica.
Br J Dermatol 2009; 161(1): 184-186.
