弘前大学大学院医学研究科 皮膚科学講座

弘前大学大学院医学研究科 皮膚科学講座


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.




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Minakawa S, Matsuzaki Y, Nakajima K, Nakano H, Sawamura D. Tegafur/gimeracil/oteracil (TS-1) induced StevenseJohnson syndrome: Case report.
Dermatologica Sinica, in press 2013
Narumi H, Nakano H, Kaneko T, Nakajima K, Matsuzaki Y, Aizu T, Sawamura D, Hanada K. Effect of cytokines and ultraviolet B radiation on the promoter activity of the metallothionein gene in keratinocytes.
Advances in Bioscience and Biotechnology, in press 2013
Nakajima K, Jin K, Kaneko T, Matsuzaki Y, Aizu T, Nakano H, Sawamura D. Cholesterotic fibrous histiocytoma with no associated dyslipidemia.
Int J Dermatol, in press 2013
Nakagawa K, Minakawa S, Sawamura D. EPR spectroscopic investigation of finger nails of nail psoriasis.
Skin Res Techonol, in press 2013
Umegaki-Arao N, Tamai K, Nimura K, Serada S, Naka T, Nakano H, Katayama I. Karyopherin alpha 2 is essential for rRNA transcription and protein synthesis in proliferative keratinocytes.
PLoS One, in press 2013 


Rokunohe D, Takeda H, Kaneko T, Aizu T, Akasaka E, Matsuzaki Y, Nakano H, Sawamura D. Spindle cell hemangioma and decorin expression.
Journal of Cosmetics, Dermatological Sciences and Applications 2012; 2: 8-10.
Natsuga K, Nishie W, Shinkuma S, Ujiie H, Nishimura M, Sawamura D, Shimizu H. Antibodies to pathogenic epitopes on type XVII collagen cause skin fragility in a complement-dependent and -independent manner.
J Immunol 2012; 188: 5792-5799.
Korekawa A, Kaneko T, Hagiwara C, Nakajima K, Takayuki A, Nakano H, Sawamura D. Angiolymphoid hyperplasia with eosinophilia in infancy.
J Dermatol 2012;39:1052-1054.
Minakawa S, Matsuzaki Y, Nakano H, Sawamura D, Elenitsas R. Acantholysis caused repeated hemorrhagic bullae in a case of acantholytic acanthoma.
J Dermatol 2012;39:1107-1108.
Itai K, Korekawa A,Jin K, Aizu T, Rokunohe A, Hagiwara C, Hanada K, Sawamura D. Effect of 0.3 – millisecond multi-pulsed 1064 – nm laser Nd:YAG in patients with postherpetic neuralgia.
Journal of Cosmetics, Dermatological Sciences and Applications. 2012;2:11-13.
Anolik RB, Elenitsas R, Minakawa S, Nguyen J, Rubin AI. Histologic features of nail cosmetics.
Am J Dermatopathol. 2012; 34: 412-415.
Yajima M, Kitoh A, Nakano H, Sawamura D, Miyachi Y, Kabashima K. Dominant dystrophic epidermolysis bullosa pruriginosa with the G2287R mutation.
Eur J Dermatol. 2012; 22: 685-687.
Umemoto H, Akiyama M, Domon T, Nomura T, Shinkuma S, Ito K, Asaka T, Sawamura D, Uitto J, Uo M, Kitagawa Y, Shimizu H. Type VII collagen deficiency causes defective tooth enamel formation due to poor differentiation of ameloblasts.
Am J Pathol. 2012; 181: 1659-1671.
Matsuzaki Y, Ota K, Sato K, Nara S, Yagushi T, Nakano H, Sawamura D. Deep Pseudocystic Dermatophytosis Caused by in a Patient with Myasthenia Gravis.
Acta Derm Venereol. 2012; 93: 358-359.
Minakawa S, Matsuzaki Y, Rokunoke D, Akasaka E, Nakajima K, Aizu T, Kaneko T, Nakano H, Takashima T, Sawamura D. A Case of Erythema Nodosum Associated with Subareolar Abscess.
Journal of Cosmetics, Dermatological Sciences and Applications. 2012; 2: 263-264.
Asahina A, Ishiko A, Saito I, Hasegawa K, Sawamura D, Nakano H
Grover’s disease following multiple bilateral Blaschko’s lines: A rare clinical presentation with genetic and electron microscopic analyses.
Dermatology. 2012; 225: 183-187.
Yajima M, Nakano H, Sawamura D, Miyachi Y, Kabashima K:Case of dominant dystrophic epidermolysis bullosa pruriginosa with a c.7868G>A (G2623D) mutation in type VII collagen.
J Dermatol. 2012; 39(: 1087-1088.
Makino E, Nakano H, Sawamura D, Fujimoto W.:Recessive dystrophic epidermolysis bullosa: Identification of a novel COL7A1 mutation of D44N.
J Dermatol Sci. 2012; 68: 109-112.
Rokunohe D, Akasaka E, Rokunohe A, Kaneko T, Matsuzaki Y, Takiyoshi N, Aizu T, Nakano H, Sawamura D: Multiple aplasia cutis congenita lesions located along Blaschko’s lines in a patient with tetralogy of Fallot-A.
J Dermatol Case Rep. 2012; 6: 40-42.
Hayashi M, Nakano H, Sawamura D, Suzuki T.Case of epidermolytic palmoplantar keratoderma with knuckle pads.
J Dermatol. 2012; 39: 84-87.
Nakagawa K, Minakawa S, Sawamura D: Spectroscopic evidence of abnormal structure of psoriasis vulgaris stratum corneum.
J Dermatol Sci. 2012; 65: 222-224.
Kimura K, Matsuzaki Y, Nishikawa Y, Kitamura H, Akasaka E, Rokunohe D, Nakano H, Imaizumi T, Satoh K, Sawamura D: Characterization of retinoic acid-inducible gene-I (RIG-I) expression corresponding to viral infection and UVB in human keratinocytes.
J Dermatolo Sci. 2012; 66: 64-70.
Koshida S, Tsukamura A, Yanagi T, Nakahara S, Takeuchi Y, Kato T, Tanaka T, Nakano H, Shimizu H. Dystrophic epidermolysis bullosa: the homozygous mutation, 5818delC in both alleles.
Pediatrics International. 2012; 55: 234-237.
Takiyoshi N, Nakano H, Sawamura D. Epidermolysis bullosa pruriginosa with marked phenotypic heterogeneity caused by a recurrent glycine substitution: Incomplete penetrance or a latent case?
J Dermatol. 2012; 39: 718-719.
Kawamura T, Ogawa Y, Nakamura Y, Nakamizo S, Izumi A, Nakano H, Kabashima K, Katayama I, Koizumi S, Kodama T, Nakao A, Shimada S. Severe irritant dermatitis with loss of Langerhans cells in a mouse model of acrodermatitis enteropathica.
J Clin Invest. 2012; 122: 722-732.
Korekawa A, Nakano H, Toyomaki Y, Takiyoshi N, Rokunohe D, Akasaka E, Nakajima K, Sawamura D: Buschke-Ollendorff syndrome associated with hypertrophic scar formation: a possible role for LEMD3 mutation.
Br J Dermato. 2012; 166(4): 900-903.
Korekawa A, Nakajima K, Nishikawa Y, Matsuzaki Y, Nakano H, Sawamura D. A late-onset, progressive eruptive syringoma in an elderly man.
Acta Derm Venereol. 2012; 92: 87-88.


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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.


Takeuchi S, NakanoH, Daiki R, Akasaka E, Nishizawa A, Matsuzaki Y, Sawamura D.Disseminated lupus vulgaris diagnosed more than 63 years after onset due to its initial misdiagnosis as a port-wine stain.
Clin Exp Dermatol 2010; 35(3): e28-29.

Jin K, Nakano H, Akasaka E, Rokunohe D, Minagawa S, Ishii N, Hashimoto T , Sawamura D. Linear immunoglobulin A bullous dermatosis possibly induced by mefenamic acid.
J Dermatol 2010; 37(5): 504.

Rokunohe D, Nakano H, Oshima H, Nakajima K, Aizu T, Kaneko T, Sawamura D. Giant cutaneous granular cell tumour with papillomatous appearance.
Clin Exp Dermatol 2010; 35(3): e7-9.

Takemoto H, Tamai K, Akasaka E, Rokunohe S, Takiyoshi N, Umegaki N, Nakajima K, Aizu T, Kaneko T, Nakano H, Sawamura S. Relation between the expression levels of the POU transcription factors Skn-1a and Skn-1n and keratinocyte differentiation.
Journal of Dermatological Science 2010; 60(3): 203-5.

Rokunohe D, Nakano H, Akasaka E, Kimura K, Takiyoshi N, Nakajima K, Aizu T, Kaneko T, Matsuzaki Y, Tsuchida S, Sawamura D. Raf kinase inhibitor protein expression correlates with differentiation but not with ERK phosphorylation in cutaneous squamous cell carcinoma.
Journal of Dermatological Science 2010; 60(3): 199-201.

Sawamura D, Goto M, Homma E, Goto-Ohguchi Y, Aoyagi S, Akiyama M, Kuroyanagi Y, Shimizu H, Natsuga K. Response of intractable skin ulcers in recessive dystrophic epidermolysis bullosa patients to an allogeneic cultured dermal substitute.
Acta Derm Venereol 2010; 90(2): 165-169.

Natsuga K, Nishie W, Akiyama M, Nakamura H, Shinkuma S, McMillan JR, Nagasaki A, Has C, Ouchi T, Ishiko A, Hirako Y, Owaribe K, Sawamura D, Bruckner-Tuderman L, Shimizu H Plectin expression patterns determine two distinct subtypes of epidermolysis bullosa simplex.
Hum Mutat 2010; 5; 31(3): 308-316.

Kimura Y, Kaneko T, Akasaka E, Nakajima K, Aizu T, Nakano H, Sawamura D: Multiple eruptive dermatofibromas associated with Hashimoto’s thyroiditis and myasthenia gravis.
EUR J Dermatol 2010; 20(4): 1-2.

Jin K, Nakano H, Akasaka E, Rokunohe D, Minagawa S, Ishii N, Hashimoto T, Sawamura D: Linear immunoglobulin A bullous dermatosis possibly induced by mefenamic acid.
J Dermatol 2010; 37(3): 269-271.

Wang G, Ujiie H, Shibaki A, Nishie W, Tateishi Y, Kikuchi K, Li Q, McMillan JR, Morioka H, Sawamura D, Nakamura H, Shimizu H Blockade of autoantibody-initiated tissue damage by using recombinant fab antibody fragments against pathogenic autoantigen.
Am J Pathol 2010; 176(2): 914-925.

Ujiie H, Shibaki A, Nishie W, Sawamura D, Wang G, Tateishi Y, Li Q, Moriuchi R, Qiao H, Nakamura H, Akiyama M, Shimizu H: A novel active mouse model for bullous pemphigoid targeting humanized pathogenic antigen.
J Immunol 2010; 184(4): 2166-2174.

Sawamura D, Nakano H, Matsuzaki Y: Overview of epidermolysis bullosa.
J Dermatol 2010; 37: 1-6.

Takeuchi S, Akasaka E, Rokunohe D, Sato-Jin K, Matsuzaki Y, Ooshima H, Nakano H, Sawamura D. Leukemia cutis is an early sign of blast transformation that may mimic a common skin disease: sycosis-like eruptions in chronic myelomonocytic leukemia.
J Dermatol 2010; 35(3): e28-29.


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.

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.

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.

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.

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.

Inokuma D, Sawamura D, Shibaki A, Abe R, Shimizu H. Scleroedema adultorum associated with sarcoidosis.
Clin Exp Dermatol 2009; 34(7): e428-429.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.


Nishizawa A, Nakano H, Satoh T, Takayama K, Sawamura D, Yokozeki H. Haber’s syndrome may be a clinical entity different from Dowling-Degos disease.
Br J Dermatol, 2008; 160(1): 215-217.

Nakano H, Akasaka E, Rokunohe D, Yokoyama S, Toyomaki Y, Umegaki N, Mitsuhashi Y, Sawamura D. A novel homozygous missense mutation in the fatty aldehyde dehydrogenase gene causes Sjogren-Larsson syndrome. 
J Dermatol Sci 2008; 52(2): 136-138.

Kivisaari AK, Kallajoki M, Mirtti T, McGrath JA, Bauer JW, Weber F, Konigova R, Sawamura D, Sato-Matsumura KC, Shimizu H, Csikos M, Sinemus K, Beckert W, Kahari VM.Transformation-specific matrix metalloproteinases (MMP)-7 and MMP-13 are expressed by tumour cells in epidermolysis bullosa-associated squamous cell carcinomas. 
Br J Dermatol 2008; 158(4): 778-85.

Nomura T, Kodama K, Moriuchi R, Yaosaka M, Kawasaki H, Abe M, Sawamura D, Shimizu H.Papuloerythroderma of Ofuji associated with early gastric cancer. 
Int J Dermatol 2008; 47(6): 590-591.

Nishie W, Sawamura D, Iitoyo M, Shimizu H.Intravascular histiocytosis associated with rheumatoid arthritis. 
Dermatology 2008; 217(2): 144-145.

Takiyoshi N, Nakano H, Kaneko T, Aizu T, Nakajima K, Akasaka E, Rokunohe D, Sawamura D. Multiple desmoplastic trichoepitheliomas with ossification and cholesterol deposition. 
Exp Dermatol 2009; 34(5): 634-635.

Minakawa S, Nakajima K, Aizu T, Nomura K, Kaimori K, A case of zosteriform metastatic skin cancer.
Clin Exp Dermatol 2008; 33(6): 808-810.

Nagasaki A, Nishie W, Sato K, Oba I, Noguchi E, Akitsu H, Sawamura D, Shimizu H. Clinical and Genetic analysis of Fabry disease: report of 6 cases including 3 heterozygous females.
J Dermatol Sci 2008; 52(1): 61-64.

Yamamoto C, Tamai K, Nakano H, Matsuzaki Y, Kaneko T, Sawamura D. Vitamin D3 inhibits expression of pemphigus vulgaris antigen, desmoglein 3: implication of partial mechanism in pharmacological effect of VD3 on skin diseases. 
Mol Med Rep 2008; 1: 581-583.

Kitamura H, Kaneko T, Nakano H, Terui H, Ito E, Sawamura D. Juvenile myelomonocytic leukemia presenting multiple painful erythematous lesions diagnosed as Sweet’s syndrome.
J Dermatol 2008; 35: 368-370.

Kakizaki I, Itano N, Kimata K, Hanada K, Kon A, Yamaguchi M, Takahashi T, Takagaki KFUp-regulation of hyaluronan synthase genes in cultured human epidermal keratinocytes by UVB irradiation.
Arch Biochem Biophys 2008; 471(1): 85-93.

Nanashima N, Akita M, Yamada T, Shimizu T, Nakano H, Fan Y, Tsuchida S.The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes. 
J Biol Chem 2008; 283(24): 16868-16875.

Nishizawa A, Nakajima R, Nakano H, Sawamura D, Takayama K, Satoh T, Yokozeki H. A de novo missense mutation in the keratin 13 gene in oral white sponge nevus.
Br J Dermatol 2008; 159(4): 974-975.

Rokunohe A, Nakano H, Aizu T, Kaneko T, Nakajima K, Ikenaga S, Matsuzaki Y, Murai T, Tamai K, Sawamura D. Significance of sentinel node biopsy in the management of squamous cell carcinoma arising from recessive dystrophic epidermolysis bullosa.
J Dermatol 2008; 35(6): 336-340.

Aizu T, Tamai K, Nakano H, Rokunohe D, Toyomaki Y, Uitto J, Sawamura D. Calcineurin/NFAT-Dependent Regulation of 230-kD Bullous Pemphigoid Antigen (BPAG1) Gene Expression in Normal Human Epidermal Keratinocytes.
J Dermatol Sci 2008; 51(1): 45-51.

Nakajima K, Tamai K, Yamazaki T, Toyomaki Y, Nakano H, Uitto J, Sawamura D. Identification of Skn-1n, a splice variant that is induced by high calcium concentration and specifically expressed in normal human keratinocytes.
J Invest Dermatol 2008; 128(5): 1336-9.

Rokunohe D, Nakano H, Ikenaga S, Umegaki N, Kaneko T, Matsuhashi Y, Tandoh Y, Toyoki Y, Hakamada K, Kusumi T, Harada K, SawamuraD. Reduction in epidermal Langerhans cells in patients with necrolytic migratory erythema.
J Dermatol Sci 2008; 50(1): 76-80.

Nakajima K, Nakano H, Takiyoshi N, Rokunohe A, Ikenaga S, Aizu T, Kaneko T, Mitsuhashi Y, Sawamura D. Papillon-Lef?vre syndrome and malignant melanoma: a high incidence of melanoma development in Japanese palmoplantar keratoderma patients.
Dermatol 2008; 217(1): 58-62.

Sato-Jin K, Nishimura EK, Akasaka E, Huber W, Nakano H, Miller A, Du J, Wu M, Hanada K, Sawamura D, Fisher DE, and Imokawa G. Epistatic connections between MITF and endothelin signaling in Waardenburg syndrome and other pigmentary disorders. 
FASEB J 2008; 22(4): 1155-68.

Hamada T, Fukuda S, Ishii N, Sakaguchi S, Ishikawa T, Abe T, Yasumoto S, Hashimoto T, Nakano H, Sawamura D. Genotype-phenotype correlation in non-Hallopeau-Siemens recessive dystrophic epidermolysis bullosa: The splice site mutation c.6216+5G>T in the COL7A1 gene results in aberrant and normal splicings.
J Dermatol Sci 2008; 50(2): 147-50.

Yamamoto C, Tamai K, Nakano H, Matsuzaki Y, Kaneko T, Sawamura D. Vitamin D(3) inhibits expression of bullous pemphigoid antigen 1 through post-transcriptional mechanism without new protein synthesis.
J Dermatol Sci 2008; 50(2): 155-158.