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.