2018年(業績・論文)

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.

2017年(業績・論文)

28.  Hattori M, Shimizu A, Nakano H, Ishikawa O.
A mild phenotype of junctional epidermolysis bullosa with pyloric atresia due to a novel mutation of the ITGB4 gene.
J Dermatol, 2017. in press

27. Fujimori N, Komatsu M, Tanaka N, Iwaya M, Nakano H, Sugiura A, Yamazaki T, Shibata S, Iwaya Y, Muraki T, Ichikawa Y, Kimura T, Joshita S, Umemura T, Matsumoto A, Tanaka E. Cimetidine/lactulose therapy ameliorates erythropoietic protoporphyria-related liver injury.
Clin J Gastroenterol. 2017 Oct;10(5):452-458.

26. Yoshioka A, Fujiwara S, Kawano H, Nakano H, Nakano S, Matsui T, Katayama Y, Nishigori C.
Late-onset Erythropoietic Protoporphyria Associated with Myelodysplastic Syndrome Treated with Azacitidine.
Acta Derm Venereol. 2017. in press.

25. Akasaka E, Nakano H, Fukui T, Korekawa A, Aizu T, Sawamura D.
The first case of multiple pilomatricomas caused by somatic mutations of CTNNB1 without any associated disorder.
J Dermatol Sci. 2017 Nov;88(2):259-260.

24. Kuriyama Y, Hattori M, Mitsui T, Nakano H, Oikawa D, Tokunaga F, Ishikawa O, Shimizu A.
Generalized verrucosis caused by various human papillomaviruses in a patient with GATA2 deficiency.
J Dermatol. 2017. in press.

23. Nishikawa Y, Matsuzaki Y, Kimura K, Rokunohe A, Nakano H, Sawamura D.
Modulation of Stimulator of Interferon Genes (STING) Expression by Interferon-γ in Human Keratinocytes.
Biochem. Genet. 2017. in press.

22. Korekawa A, Nakajima K, Nakano H, Sawamura D.
Successful epithelialization of perianal infantile hemangioma, presenting as intractable ulcers, with application of protective colostomy powder.
J Dermatol. 2017; 44(10): e264-e265.

21. Jin K, Matsuzaki Y, Akasaka E, Korekawa A, Nakano H, Sawamura D.
Successful treatment of low-dose methotrexate in combination with systemic steroids for juvenile multiple and symmetrical circumscribed morphea.
J Dermatol. 2017; 44(10): e256-e257.

20. Araki Y, Abe Y, Takeda Y, Nakano H, Sawamura D, Yamashita H, Suzuki T.
Incontinentia pigmenti with retinal vascular anomaly and deletion of exons 4-10 in NEMO.
J Dermatol. 2017; 44(8): 976-977.

19. Matsuzaki Y, Kaneko T, Makita E, Rokunohe A, Minakawa S, Nakano H, Sawamura D. Postoperative maxillary cyst presenting as a skin tumour on the cheek.
Eur J Dermatol. 2017; 27(4): 433-434.

18. Nakajima K, Jin K, Kaneko T, Matsuzaki Y, Aizu T, Nakano H, Sawamura D.
Cholesterotic fibrous histiocytoma with no associated dyslipidemia.
Int J Dermatol. 2017; 56(6): e124-e126.

17.Matsuzaki Y, Yokoyama S, Rokunohe A, Minakawa S, Nakano H, Sawamura D.
Successful treatment of Kyrle disease with narrowband ultraviolet B.
J Dermatol. 2017; 44(6): 721-722.

16. Korekawa A, Nakajima K, Makita E, Nakano H, Sawamura D.
External chalazion as reddish and intractable lower eyelid nodules in a child.
J Dermatol. 2017; 44(5): e93-e94.

15. Li M, Higashi N, Nakano H, Saeki H.
An ATP2A2 Missense Mutation in a Japanese Family with Darier Disease: A Case Report and Review of the Japanese Darier Disease Patients with ATP2A2 Mutations.
J Nippon Med Sch. 2017; 84(5): 246-250.

14. Mizawa M, Makino T, Furukawa F, Torai R, Nakano H, Sawamura D, Shimizu T.
The 6-year follow-up of a Japanese patient with silent erythropoietic protoporphyria.
JAAD Case Rep. 2017; 3(3): 169-171.

13. Murakami Y, Sakai S, Takeda K, Sawamura D, Yoshida K, Hirose T, Ikeda C, Mani H, Yamamoto T, Ito A.
Autistic traits modulate the activity of the ventromedial prefrontal cortex in response to female faces.
Neurosci Res. 2017: S0168-0102(17)30467-30464.

12. Toyonaga E, Nishie W, Izumi K, Natsuga K, Ujiie H, Iwata H, Yamagami J, Hirako Y, Sawamura D, Fujimoto W, Shimizu H. C-Terminal Processing of Collagen XVII Induces Neoepitopes for Linear IgA Dermatosis Autoantibodies.
J Invest Dermatol. 2017; 137(12): 2552-2559.

11. Matsuzaki Y, Rokunohe A, Minakawa S, Nomura K, Nakano H, Ito E, Sawamura D.
Incontinentia pigmenti in a male (XY) infant with long-term follow up over 8 years.
J Dermatol. 2017 in press.

10. Fukui T, Kitamura H, Harada K, Nakano H, Sawamura D.  Trichoscopic Findings of Erosive Pustular Dermatosis of the Scalp Associated with Gefitinib.
Case Rep Dermatol. 2017; 9(2): 44-49.

9. Minakawa S, Kaneko T, Matsuzaki Y, Yamada M, Kayaba H, Sawamura D.
Psoriasis Area and Severity Index is closely related to serum C-reactive protein level and neutrophil to lymphocyte ratio in Japanese patients.
J Dermatol. 2017; 44(10): e236-e237.

8. Takadama S, Nakaminami H, Aoki S, Akashi M, Wajima T, Ikeda M, Mochida A, Shimoe F, Kimura K, Matsuzaki Y, Sawamura D, Inaba Y, Oishi T, Nemoto O, Baba N, Noguchi N.
Prevalence of skin infections caused by Panton-Valentine leukocidin-positive methicillin-resistant Staphylococcus aureus in Japan, particularly in Ishigaki, Okinawa.
J Infect Chemother. 2017; 23(11): 800-803.

7. Akasaka E, Nakano H, Takagi Y, Toyomaki Y, Sawamura D. Multiple Milia as an Isolated Skin Manifestation of Dominant Dystrophic Epidermolysis Bullosa: Evidence of Phenotypic Variability.
Pediatr Dermatol. 2017; 34(2): e106-e108.

6. Matsui A, Kaneko T, Takiyoshi N, Rokunohe D, Nakano H, Sawamura D.
Juvenile temporal arteritis with eosinophilia associated with systemic sclerosis.
J Dermatol. 2017; 44(3): e50-e51.

5. Korekawa A, Nakajima K, Nakano H, Sawmura D.
Translucent basal cell carcinoma with a single cyst of the upper eyelid.
J Dermatol. 2017; 44(10): e264-e265.

4. Murakami Y, Wataya-Kaneda M, Iwatani Y, Kubota T, Nakano H, Katayama I.
Novel mutation of OCRL1 in Lowe syndrome with multiple epidermal cysts.
J Dermatol. 2017.  in press.

3. Fujii A, Matsuyama K, Mizutani Y, Kanoh H, Nakano H, Seishima M.M
ultiple familial trichoepithelioma with a novel mutation of CYLD gene.
J Dermatol 2017; 44(9): e228-e229.

2. Hattori M, Shimizu A, Oikawa D, Kamei K, Kaira K, Yamamoto A, Nakano H, Sawamura D, Tokunaga F, Ishikawa O.
ER stress in the pathogenesis of pretibial dystrophic epidermolysis bullosa.
Br J Dermatol. 2017; 177(4): e92-e93.

1.  Suzuki H, Kikuchi K, Fukuhara N, Nakano H, Aiba S.
Case of late-onset erythropoietic protoporphyria with myelodysplastic syndrome who has homozygous IVS3-48C polymorphism in the ferrochelatase gene.
J Dermatol. 2017; 44(6): 651-655.

 

2016年(業績・論文)

15.Araki Y, Abe Y, Takeda Y, Nakano H, Sawamura D, Yamashita H, Suzuki T. Incontinentia pigmenti with retinal vascular anomaly and deletion of exons 4-10 in NEMO.
J Dermatol. 2016 in press.

14. Akasaka E, Hagiwara C, Takiyoshi N, Aizu T, Ota T, Nakano H, Sawamura D. Elevated levels of circulating immunoglobulin E autoantibodies against BP180 and BP230 in an intractable case of bullous pemphigoid
J Dermatol Sci. 2016 in press.

13.Ninomiya Y, Kokunai Y, Tanizaki H, Akasaka E, Nakano H, Moriwaki S. X-linked dominant protoporphyria: The first reported Japanese case.
J Dermatol. 2016; 43(4): 414-418.

12. Rokunohe D, Nakano H, Akasaka E, Toyomaki Y, Sawamura D. Rubinstein-Taybi syndrome with multiple pilomatricomas: The first case diagnosed by CREBBP mutation analysis.
J Dermatol Sci. 2016 in press.

11.Fukui T, Sakuraba Y, Harada K, Nakano H, Sawamura D. Moth-Eaten Symptomatic Syphilitic Alopecia Associated with Human Immunodeficiency Virus―A Case Report.
Case Rep Clin Med. 2016; 5(5): 188-190.

10. Mizawa M, Makino T, Nakano H, Sawamura D, Shimizu T. Incomplete erythropoietic protoporphyria caused by a splice site modulator homozygous IVS3-48C polymorphism in the ferrochelatase gene.
Br J Dermatol. 2016; 174(1): 172-175.

9. Inoue N, Dainichi T, Fujisawa A, Nakano H, Sawamura D, Miyachi Y, Kabashima K. CARD14 Glu138 mutation in familial pityriasis rubra pilaris does not warrant differentiation from familial psoriasis. J Dermatol. 2016; 43(2): 187-189.

8. Matsuzaki Y, Jin K, Rokunohe A, Minakawa S, Nakano H, Sawamura D. Annular leukocytoclastic vasculitis associated with essential mixed cryoglobulinemia.
Eur J Dermatol. 2016. in press

7. Kaneko T, Rokunohe D, Takiyoshi N, Minakawa S, Nakano H, Sawamura D. Usefulness of ultrasonography in the diagnosis of ischaemic fasciitis.
Clin Exp Dermatol. 2016. in press

6. Takahashi T, Mizutani Y, Ito M, Nakano H, Sawamura D, Seishima M. Dystrophic epidermolysis bullosa pruriginosa successfully treated with immunosuppressants.
J Dermatol. 2016. in press

5. Korekawa A, Nakajima K, Nakano H, Sawamura D.
Subcutaneous histiocytoid Sweet’s syndrome followed by acute myelocytic leukemia.
J Dermatol. 2016. in press

4. Makita E, Akasaka E, Sakuraba Y, Korekawa A, Aizu T, Kaneko T, Nakano H, Sawamura D. Squamous cell carcinoma on the lip arising from discoid lupus erythematosus: a case report and review of Japanese patients.
Eur J Dermatol. 2016. in press

3. Adachi T, Tanese K, Ouchi T, Igawa S, Nakano H, Ishiko A.
Case of isolated epidermolytic acanthoma: Genetic and immunohistochemical analysis.
J Dermatol. 2016. in press

2. Rokunohe A, Matsuzaki Y, Rokunohe D, Sakuraba Y, Fukui T, Nakano H, Sawamura D. Immunosuppressive effect of adipose-derived stromal cells on imiquimod-induced psoriasis in mice.
J Dermatol Sci. 2016 Apr;82(1):50-3.

1. Kaneko T, Korekawa A, Akasaka E, Nakano H, Sawamura D. Amelanotic acral lentiginous melanoma mimicking diabetic ulcer: a challenge to diagnose and treat.
Eur J Dermatol. 2016 Feb 1;26(1):107-8.

2015年(業績・論文)

17. Kinjyo C, Kaneko T, Korekawa A, Rokunohe A, Aizu T, Matsuzaki Y, Nakano H, Sawamura D.
Oral lichen planus with antibodies to desmogleins 1 and 3.
J Dermatol. 2015 Jan;42(1):40-1.

16.  Jin K, Matsuzaki Y, Korekawa A, Rokunohe A, Aizu T, Kinjyo C, Nakano H, Sawamura D. Pompholyx-like manifestation in Churg-Strauss syndrome.
Eur J Dermatol. 2015 Apr;25(2):188-9.

15. Yamamoto T, Hasegawa T, Nakano H.Acquired localized cutis laxa occurring on the face after delivery.
Eur J Dermatol. 2015 May-Jun;25(3):266-7.

14. Korekawa A, Nakano H, Aizu T, Kitamura H, Harada K, Sawamura D. A reddish, pedunculated, granulomatous nodule on the nasal dorsum.
Clin Exp Dermatol. 2015 Aug;40(6):703-5.

13.  Akasaka E, Okawa Y, Nakano H, Takiyoshi N, Rokunohe D, Toyomaki Y, Sawamura D, Sueki H. Two Japanese familial cases of punctate palmoplantar keratoderma caused by a novel AAGAB mutation, c.191_194delCAAA.
J Dermatol Sci. 2015 May;78(2):156-8.

12. Akasaka E, Minakawa S, Rokunohe D, Toyomaki Y, Matsuzaki Y, Sawamura D, Nakano H. Superficial epidermolytic ichthyosis caused by a novel KRT2 mutation.
J Dermatol Sci. 2015 Jul;79(1):86-8.

11. Korekawa A, Kaneko T, Nakajima K, Rokunohe D, Akasaka E, Nakano H, Sawamura D, Fukui T, Takiyoshi N, Kitamura H, Harada K. Mycosis fungoides bullosa associated with bullous pemphigoid.
Int J Dermatol. 2015 Sep;54(9):e366-8.

10. Makino T, Shimizu K, Mizawa M, Nakano H, Sawamura D, Shimizu T. A novel deletion mutation of the ATP2C1 gene in a family with Hailey-Hailey disease.
Eur J Dermatol. 2015. in press

9. Korekawa A, Nakano H, Sawamura D, Kitamura H, Harada K.
Erythema induratum of Bazin in a patient with scrofuloderma.
Eur J Dermatol. 2015 Sep-Oct;25(5):512-3.

8. Akasaka E, Jin K, Nakano H, Ishii N, Hashimoto T, Sawamura D. Diaminodiphenyl Sulfone-Induced Hemolytic Anemia and Alopecia in a Case of Linear IgA Bullous Dermatosis.
Case Rep Dermatol. 2015 Jul 25;7(2):183-6.

7. Aizu T, Matsui A, Takiyoshi N, Akasaka E, Kaneko T, Nakano H, Sugiura K, Akiyama M, Sawamura D. Elderly-Onset Generalized Pustular Psoriasis without a Previous History of Psoriasis Vulgaris.
Case Rep Dermatol. 2015 Jul 29;7(2):187-93.

6. Korekawa A, Nakajima K, Aizu T, Nakano H, Sawamura D.
Blue Rubber Bleb Nevus Syndrome Showing Vascular Skin Lesions Predominantly on the Face.
Case Rep Dermatol. 2015 Jul 29;7(2):194-8.

5. Kaneko T, Korekawa A, Akasaka E, Rokunohe D, Nakano H, Sawamura D. Primary Amelanotic Rhabdoid Melanoma: A Case Report with Review of the Literature.
Case Rep Dermatol. 2015 Oct 10;7(3):292-7.

4. Korekawa A, Nakajima K, Kaneko T, Nakano H, Sawamura D.
Discoid lupus erythematosus with dystrophic calcinosis cutis.
JAAD Case Rep. 2015 Jun 9;1(4):182-184.

3. Koguchi-Yoshioka H, Wataya-Kaneda M, Yutani M, Murota H, Nakano H, Sawamura D, Katayama I. Atopic Diathesis in Hypohidrotic/Anhidrotic Ectodermal Dysplasia.
Acta Derm Venereol. 2015; 95: 476–9.

2. Koguchi-Yoshioka H, Wataya-Kaneda M, Nakano H, Tanemura A, Akasaka E, Sawamura D, Katayama I. Severe scoliosis associated with the WNT10A mutation.
J Dermatol. 2015; 42: 322-3.

1. Akasaka E, Nakano H, Korekawa A, Fukui T, Kaneko T, Koga H, Hashimoto T, Sawamura D. Anti-laminin γ1 pemphigoid associated with ulcerative colitis and psoriasis vulgaris showing autoantibodies to laminin γ1, type XVII collagen and laminin-332.
Eur J Dermatol. 2015; 25(2): 198-199.

2014年(業績・論文)

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.

2013年(業績・論文)

5.
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
4.
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
3.
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
2.
Nakagawa K, Minakawa S, Sawamura D. EPR spectroscopic investigation of finger nails of nail psoriasis.
Skin Res Techonol, in press 2013
1.
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 

2012年(業績・論文)

22.
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.
21.
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.
20.
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.
19.
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.
18.
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.
17.
Anolik RB, Elenitsas R, Minakawa S, Nguyen J, Rubin AI. Histologic features of nail cosmetics.
Am J Dermatopathol. 2012; 34: 412-415.
16.
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.
15.
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.
14.
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.
13.
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.
12.
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.
11.
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.
10.
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.
9.
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.
8.
Hayashi M, Nakano H, Sawamura D, Suzuki T.Case of epidermolytic palmoplantar keratoderma with knuckle pads.
J Dermatol. 2012; 39: 84-87.
7.
Nakagawa K, Minakawa S, Sawamura D: Spectroscopic evidence of abnormal structure of psoriasis vulgaris stratum corneum.
J Dermatol Sci. 2012; 65: 222-224.
6.
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.
5.
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.
4.
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.
3.
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.
2.
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.
1.
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.

2011年(業績・論文)

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.

2010年(業績・論文)

13.
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.

12.
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.

11.
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.

10.
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.

9.
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.

8.
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.

7.
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.

6.
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.

5.
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.

4.
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.

3.
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.

2.
Sawamura D, Nakano H, Matsuzaki Y: Overview of epidermolysis bullosa.
J Dermatol 2010; 37: 1-6.

1.
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.

2009年(業績・論文)

18.
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.
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.
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.
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.
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.
Inokuma D, Sawamura D, Shibaki A, Abe R, Shimizu H. Scleroedema adultorum associated with sarcoidosis.
Clin Exp Dermatol 2009; 34(7): e428-429.

12.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.