Papers - AKASAKA Eijiro
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Availability of mRNA Obtained from Peripheral Blood Mononuclear Cells for Testing Mutation Consequences in Dystrophic Epidermolysis Bullosa
Eijiro Akasaka, Hajime Nakano, Daisuke Sawamura
International Journal of Molecular Science 2021.12
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Diversity of Mechanisms Underlying Latent TGF-β Activation in Recessive Dystrophic Epidermolysis Bullosa.
Akasaka E, Kleiser S, Sengle G, Bruckner-Tuderman L, Nyström A
The Journal of investigative dermatology 141 ( 6 ) 1450 - 1460.e9 2021.6
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Lymphomatoid Papulosis Following Spesolimab Treatment for Generalised Pustular Psoriasis
Namba, M; Matsumoto, M; Saito, N; Kimura, A; Sagara, C; Rokunohe, D; Akasaka, E
AUSTRALASIAN JOURNAL OF DERMATOLOGY 2025.6
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特集 アトピー性皮膚炎と誤診される皮膚疾患 臨床例 軽症アトピー性皮膚炎を合併した長島型掌蹠角化症
赤坂 英二郎
皮膚病診療 47 ( 5 ) 402 - 406 2025.5
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A sporadic case of glomuvenous malformation harboring a novel mutation in GLMN.
Terada A, Akasaka E
The Journal of dermatology 2025.1
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A Japanese case of Papillon-Lefèvre syndrome diagnosed by pyogenic liver abscess.
Terada A, Murai T, Akasaka E
The Journal of dermatology 2025.1
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皮心伝心 積み重ねが大切,1つずつ丁寧に
赤坂 英二郎
皮膚病診療 46 ( 12 ) 1117 - 1117 2024.12
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A case of mucous membrane pemphigoid solely with IgA anti-BP230 antibodies detected by immunoblotting using normal human epidermal extracts.
Minakawa S, Matsuzaki Y, Hashimoto T, Ishii N, Sawamura D, Akasaka E
The Journal of dermatology 2024.10
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Successful treatment of Bothnian-type palmoplantar keratoderma using the etretinate and goreisan combination.
Oshimo T, Hamada R, Ono C, Fukai K, Akasaka E, Tsuruta D
The Journal of dermatology 2024.10
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高齢者に多い皮膚疾患 感染症を中心に
赤坂英二郎
弘前市医師会報 59 ( 3 ) 55 - 61 2024.6
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Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
Minakawa S, Matsuzaki Y, Higashino T, Suzuki T, Tomita H, Akasaka E, Sawamura D.
Front Med 11 1374222 2024.5
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A case of Hailey-Hailey disease with novel ATP2C1 gene variant (c.G925C) showing unusual phenotype.
Satoko Minakawa, Yasushi Matsuzaki, Toshihide Higashino, Nanako Yamada, Tamio Suzuki, Eijiro Akasaka, Daisuke Sawamura
The Journal of dermatology 51 ( 10 ) e346 - e348 2024.5
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症例 遺伝子診断により確定した点状掌蹠角化症1A型の1例
飯島 茂子, 髙山 典子, 赤坂 英二郎, 中野 創
皮膚科の臨床 66 ( 5 ) 605 - 609 2024.5
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A case of dominant dystrophic epidermolysis bullosa pruriginosa with a novel mutation in the hinge region of <i>COL7A1</i>
Ida, A; Ishikawa, O; Uchiyama, A; Akasaka, E
JOURNAL OF CUTANEOUS IMMUNOLOGY AND ALLERGY 7 2024.5
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Pyoderma gangrenosum successfully treated with split-thickness skin grafting in combination with negative pressure wound therapy: A case report
Saito N, Sagara C, Terada A, Akasaka E, Nakano H, Nakajima K, Sawamura D
J Dermatol 2024.5
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【太陽光線と皮膚】(Part4)遺伝性光線過敏症 常染色体潜性(劣性)遺伝性の多様性(異型)ポルフィリン症
赤坂英二郎
23 ( 6 ) 561 - 563 2024.5
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Upregulated expression of glucose transporter isoform 1 in invasive and metastatic extramammary Paget's disease.
Mika Matsumoto, Daiki Rokunohe, Takanori Sasaki, Yasushi Matsuzaki, Hajime Nakano, Hiroki Mizukami, Eijiro Akasaka, Daisuke Sawamura
Experimental and therapeutic medicine 27 ( 5 ) 228 - 228 2024.5
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【太陽光線と皮膚】(Part4)遺伝性光線過敏症 後天性赤芽球性(骨髄性)プロトポルフィリン症
関根 千香子, 中野 創, 赤坂 英二郎, 森脇 真一
23 ( 6 ) 564 - 567 2024.5
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マイオピニオン 新米教授のつぶやき-弘前より,今後の抱負として
赤坂 英二郎
臨床皮膚科 78 ( 4 ) 282 - 283 2024.4
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Cellular localization of glucose transporters in seborrheic keratosisclinicopathological analysis
Matsumoto Mika, Rokunohe Daiki, Kogawa Kazuhito, Matsuzaki Yasushi, Sasaki Takanori, Nakano Hajime, Mizukami Hiroki, Akasaka Eijiro, Sawamura Daisuke
Hirosaki Medical Journal 74 ( 1-4 ) 108 - 116 2024.3
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Variable clinical consequences of mosaicism for c.1167dupC in IKBKG in male and female patients with incontinentia pigmenti and related phenotypes.
Roy Luister C Acos, Yi-Han Chang, Yu-Chen Lin, Dianne Katherine R Salazar-Paras, Yu Fujimura, Hajime Nakano, Eijiro Akasaka, Ken Natsuga, Bryan Edgar K Guevara, John A McGrath, Chao-Kai Hsu
Clinical and experimental dermatology 49 ( 3 ) 298 - 301 2024.2
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Acquired cutis laxa secondary to acute generalized exanthematous pustulosi
Yamashita A, Fukui T, Akasaka E, Nakajima K, Nakano H, Hamaya T, Sawamura D
21 ( 2 ) 287 - 293 2024.2
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Malignant melanoma originating in an area affected by Mal de Meleda : A case report
SAKAMOTO Shoichi, YAMAMOTO Yuki, MURAOKA Kyoko, YARIYAMA Azusa, HARA Tomoyuki, INABA Yutaka, NAKANO Hajime, AKASAKA Eijiro, JINNIN Masatoshi
Skin Cancer 39 ( 1 ) 8 - 13 2024
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Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient.
Satoko Minakawa, Yasushi Matsuzaki, Toshihide Higashino, Tamio Suzuki, Hirofumi Tomita, Eijiro Akasaka, Daisuke Sawamura
Frontiers in medicine 11 1374222 - 1374222 2024
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Activities of the Research Group for Comprehensive Research of Gene Mutation-related Rare and Intractable Diseases of the Skin within the Project for Research on Intractable Diseases of the Ministry of Health, Labor, and Welfare of Japan
Hashimoto Takashi, Moriwaki Shin-ichi, Iwata Hiroaki, Furumura Minao, Hayama Koremasa, Kanazawa Nobuo, Kambe Naotomo, Nomura Toshifumi, Yoneda Kozo, Kawakami Tamihiro, Nakano Hajime, Akasaka Eijiro, Tateishi Chiharu, Ota Keiko, Shintani Ayumi, Tsuruta Daisuke
The Keio Journal of Medicine advpub ( 0 ) 2024
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Two cases of the intermediate phenotype of recessive dystrophic epidermolysis bullosa harboring the novel COL7A1 mutation c.3570G>A
Akasaka E, Nakano H, Sawamura D
Journal of Dermatological Science 106 ( 3 ) 193 - 195 2023.11
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【角化症を知る】表皮融解性魚鱗癬と表在性表皮融解性魚鱗癬
赤坂英二郎
皮膚科 2023.8
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症例報告 ペムブロリズマブおよびDPP-4阻害薬ビルダグリプチンの長期投与中に生じた水疱性類天疱瘡の1例
福士 花恋, 福井 智久, 赤坂 英二郎, 滝吉 典子, 中島 康爾, 中野 創, 澤村 大輔, 村井 孝弥, 泉 健太郎, 石井 文人
臨床皮膚科 77 ( 6 ) 407 - 412 2023.5
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Two cases of cutaneous-type pemphigus vulgaris and a case of pemphigus foliaceus without mucosal involvement despite high anti-desmoglein 3 autoantibody levels
Terada A, Akasaka E, Nakano H, Sawamura D
51 ( 3 ) 1501 - 1505 2023.5
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A case of epidermolysis bullosa acquisita with IgG and IgM anti-basement membrane zone antibodies relapsed after COVID-19 mRNA vaccination
Minakawa S, Matsuzaki Y, Yao S, Sagara C, Akasaka E, Koga H, Ishii N, Hashimoto T, Sawamura D
Front Med 2023.5
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A case of adult-onset localized recessive dystrophic epidermolysis bullosa, harboring the novel COL7A1 mutation p.G2754E and the previously reported mutation p.R1763
J Dermatol. 51 ( 3 ) e74 - e76 2023.4
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特集 角化症～角質の科学から考える～ 臨床例 Cowden病における両口角の角化性乳頭腫状病変
山下 あや, 赤坂 英二郎, 中野 創, 澤村 大輔, 福井 誠
皮膚病診療 45 ( 3 ) 246 - 249 2023.3
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Eruptive melanocytic nevi associated with encorafenib and cetuximab combination therapy
J Dermatol. 2022.12
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Author reply to "WNT10A variant and severe scoliosis?".
J Dermatol. 2022.11
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Erratum to "Two cases of the intermediate phenotype of recessive dystrophic epidermolysis bullosa harbouring the novel COL7A1 mutation c.3570G>A" [J. Dermatol. Sci. 106(3) (2022) 193-195].
Eijiro Akasaka, Hajime Nakano, Daisuke Sawamura
Journal of dermatological science 108 ( 1 ) 55 - 55 2022.10
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Dystrophic calcinosis cutis in a patient with cutaneous sarcoidosis in remission
Skin Health Dis. 2022.9
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Nonepisodic angioedema with eosinophilia with remarkably high blood eosinophil counts
JAAD Case Rep 2022.9
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A mild case of acute generalized exanthematous pustulosis caused by gemcitabine
J Dermatol. 2022.8
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Kindler epidermolysis bullosa associated with oral cancer in the buccal mucosa.
Akasaka E, Nakano H, Sawamura D.
JAAD Case Rep 2022.6
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Two cases of the intermediate phenotype of recessive dystrophic epidermolysis bullosa harboring the novel COL7A1 mutation c.3570G>A
J Dermatol Sci. 2022.6
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点状掌蹠角化症IA型の親子例
小泉 滋, 中村 聡子, 中野 創, 赤坂 英二郎, 中野 倫代
皮膚科の臨床 2022.6
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症例 点状掌蹠角化症ⅠA型の親子例
小泉 滋, 中村 聡子, 中野 創, 赤坂 英二郎, 中野 倫代
皮膚科の臨床 64 ( 6 ) 1074 - 1078 2022.5
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Novel mutation of the ferrochelatase gene in a Japanese boy with erythropoietic protoporphyria
Munemoto S, Tsuchihara K, Fujishima C, Hioki C, Sasaki H, Yoshida H, Akasaka E, Nakano H, Kudo H.
2022.5
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A 1,035-Subject Study Suggesting a History of Bone Fracture as a Possible Factor Associated with the Development of Anti-BP180 Autoantibodies
142 984 - 987 2021.11
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Pembrolizumab-Induced Lichen Planus on the Scalp of a Patient with Non-Small-Cell Lung Carcinoma
Aya Yamashita, Eijiro Akasaka, Hajime Nakano, Daisuke Sawamura
13 ( 3 ) 487 - 491 2021.8
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症例 副乳全切除時の病理検査にて偶然発見された線維腺腫
高橋 実か, 是川 あゆ美, 赤坂 英二郎, 中野 創, 澤村 大輔
皮膚科の臨床 63 ( 2 ) 233 - 236 2021.2
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Analysis of the mechanism underlying a mild phenotype of hereditary coproporphyria due to a homozygous missense mutation in the transcription initiation codon of the coproporphyrinogen III oxidase gene.
Tomohisa Fukui, Eijiro Akasaka, Daiki Rokunohe, Yasushi Matsuzaki, Daisuke Sawamura, Kenji Kabashima, Hajime Nakano
Journal of dermatological science 100 ( 2 ) 156 - 159 2020.11
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Abnormal keratinization and cutaneous inflammation in Mal de Meleda.
Mari Kudo, Nobuko Ishiura, Miwa Tamura-Nakano, Teruo Shimizu, Masahiro Kamata, Eijiro Akasaka, Hajime Nakano, Yoshiaki Okuma, Yayoi Tada, Hitoshi Okochi, Takeshi Tamaki
The Journal of dermatology 47 ( 5 ) 554 - 558 2020.5
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Pyoderma gangrenosum triggered by switching from adalimumab to secukinumab.
Kayo Jin, Yasushi Matsuzaki, Eijiro Akasaka, Hajime Nakano, Daisuke Sawamura
The Journal of dermatology 46 ( 3 ) e108 - e109 2019.3
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Nagashima-type palmoplantar keratoderma and malignant melanoma in Japanese patients.
A Korekawa, E Akasaka, D Rokunohe, T Fukui, T Kaneko, D Sawamura, M Ishikawa, T Yamamoto, H Nakano
The British journal of dermatology 180 ( 2 ) 415 - 416 2019.2
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特集 小児先天性皮膚疾患 臨床例 先天性爪甲硬厚症─ケラチン6a遺伝子変異による孤発例─
赤坂 英二郎, 馬場 由香, 中野 創, 澤村 大輔
皮膚病診療 41 ( 1 ) 53 - 56 2019.1
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The first Japanese case of familial porphyria cutanea tarda diagnosed by a UROD mutation.
Akinobu Matsui, Eijiro Akasaka, Daiki Rokunohe, Yasushi Matsuzaki, Daisuke Sawamura, Hajime Nakano
Journal of dermatological science 93 ( 1 ) 65 - 67 2019.1
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Novel mutation c.263A>G in the ACVRL1 gene in a Japanese patient with hereditary hemorrhagic telangiectasia 2.
Yaginuma A, Itoh M, Akasaka E, Nakano H, Sawamura D, Nakagawa H, Asahina A
The Journal of dermatology 46 ( 1 ) e22 - e24 2019.1
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The first Japanese case of familial porphyria cutanea tarda diagnosed by a UROD mutation.
Matsui A, Akasaka E, Rokunohe D, Matsuzaki Y, Sawamura D, Nakano H
Journal of dermatological science 93 ( 1 ) 65 - 67 2019.1
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Cross-sectional survey on disease severity in Japanese patients with harlequin ichthyosis/ichthyosis: Syndromic forms and quality-of-life analysis in a subgroup.
Murase C, Takeichi T, Shibata A, Nakatochi M, Kinoshita F, Kubo A, Nakajima K, Ishii N, Amano H, Masuda K, Kawakami H, Kanekura T, Washio K, Asano M, Teramura K, Akasaka E, Tohyama M, Hatano Y, Ochiai T, Moriwaki S, Sato T, Ishida-Yamamoto A, Seishima M, Kurosawa M, Ikeda S, Akiyama M
Journal of dermatological science 92 ( 2 ) 127 - 133 2018.11
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Irreversible bilateral cyanosis of the hands caused by hypothenar hammer syndrome with systemic sclerosis.
Kayo Jin, Yasushi Matsuzaki, Eijiro Akasaka, Tomohisa Fukui, Chihiro Sagara, Hajime Nakano, Daisuke Sawamura
European journal of dermatology 28 ( 4 ) 525 - 526 2018.8
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Novel mutation c.263A>G in the ACVRL1 gene in a Japanese patient with hereditary hemorrhagic telangiectasia 2
Aya Yaginuma, Munenari Itoh, Eijiro Akasaka, Hajime Nakano, Daisuke Sawamura, Hidemi Nakagawa, Akihiko Asahina
Journal of Dermatology 2018.6
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The first case of multiple pilomatricomas caused by somatic mutations of CTNNB1 without any associated disorder.
Eijiro Akasaka, Hajime Nakano, Tomohisa Fukui, Ayumi Korekawa, Takayuki Aizu, Daisuke Sawamura
Journal of dermatological science 88 ( 2 ) 259 - 260 2017.11
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Successful treatment of low-dose methotrexate in combination with systemic steroids for juvenile multiple and symmetrical circumscribed morphea.
Kayo Jin, Yasushi Matsuzaki, Eijiro Akasaka, Ayumi Korekawa, Hajime Nakano, Daisuke Sawamura
The Journal of dermatology 44 ( 10 ) e256 - e257 2017.10
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Epub 2017 Jun 30. Successful treatment of low-dose methotrexate in combination with systemic steroids for juvenile multiple and symmetrical circumscribed morphea
Kayo Jin, Yasushi Matsuzaki, Eijiro Akasaka , Ayumi Korekawa, Hajime Nakano, Daisuke Sawamura
Journal of Dermatology 44 ( 10 ) e256 - e257 2017.10
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Multiple Milia as an Isolated Skin Manifestation of Dominant Dystrophic Epidermolysis Bullosa: Evidence of Phenotypic Variability.
Eijiro Akasaka, Hajime Nakano, Yuriko Takagi, Yuka Toyomaki, Daisuke Sawamura
Pediatric dermatology 34 ( 2 ) e106 - e108 2017.6
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Elevated levels of circulating immunoglobulin E autoantibodies against BP180 and BP230 in an intractable case of bullous pemphigoid.
Eijiro Akasaka, Chihiro Hagiwara, Noriko Takiyoshi, Takayuki Aizu, Hajime Nakano, Daisuke Sawamura, Toshiaki Ota
Journal of dermatological science 84 ( 1 ) 110 - 113 2016.10
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Rubinstein-Taybi syndrome with multiple pilomatricomas: The first case diagnosed by CREBBP mutation analysis.
Daiki Rokunohe, Hajime Nakano, Eijiro Akasaka, Yuka Toyomaki, Daisuke Sawamura
Journal of dermatological science 83 ( 3 ) 240 - 242 2016.9
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Squamous cell carcinoma on the lip arising from discoid lupus erythematosus: a case report and review of Japanese patients.
Eiko Makita, Eijiro Akasaka, Yusuke Sakuraba, Ayumi Korekawa, Takayuki Aizu, Takahide Kaneko, Hajime Nakano, Daisuke Sawamura
European journal of dermatology : EJD 26 ( 4 ) 395 - 396 2016.8
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【似たもの同士:目で見る鑑別診断2016-水疱性病変編】 (Part4.)下肢(case 14) 優性栄養障害型表皮水疱症(痒疹型)vs結節性痒疹(解説/特集)
赤坂英二郎、滝吉典子、中野 創、澤村大輔
Visual Dermatology 15 ( 7 ) 715 - 717 2016.6
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X-linked dominant protoporphyria: The first reported Japanese case.
Ninomiya Y, Kokunai Y, Tanizaki H, Akasaka E, Nakano H, Moriwaki S
The Journal of dermatology 43 ( 4 ) 414 - 8 2016.4
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Amelanotic acral lentiginous melanoma mimicking diabetic ulcer: a challenge to diagnose and treat.
Takahide Kaneko, Ayumi Korekawa, Eijiro Akasaka, Hajime Nakano, Daisuke Sawamura
European journal of dermatology : EJD 26 ( 1 ) 107 - 108 2016.2
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Primary Amelanotic Rhabdoid Melanoma: A Case Report with Review of the Literature.
Kaneko T, Korekawa A, Akasaka E, Rokunohe D, Nakano H, Sawamura D
Case Reports in Dermatology 2015.10
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X-linked dominant protoporphyria: The first reported Japanese case.
Ninomiya Y, Kokunai Y, Tanizaki H, Akasaka E, Nakano H, Moriwaki S.
Journal of Dermatology 2015.9
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Mycosis fungoides bullosa associated with bullous pemphigoid.
Korekawa A, Kaneko T, Nakajima K, Rokunohe D, Akasaka E, Nakano H, Sawamura D, Fukui T, Takiyoshi N, Kitamura H, Harada K
International Journal of Dermatology 2015.9
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Primary Amelanotic Rhabdoid Melanoma: A Case Report with Review of the Literature.
Kaneko T, Korekawa A, Akasaka E, Rokunohe D, Nakano H, Sawamura D
Case reports in dermatology 7 ( 3 ) 292 - 7 2015.9
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Elderly-Onset Generalized Pustular Psoriasis without a Previous History of Psoriasis Vulgaris
Aizu T, Matsui A, Takiyoshi N, Akasaka E, Kaneko T, Nakano H, Sugiura K, Akiyama M, Sawamura D
Case Reports in Dermatology 2015.7
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Diaminodiphenyl Sulfone-Induced Hemolytic Anemia and Alopecia in a Case of Linear IgA Bullous Dermatosis
Akasaka E, Kayo SJ, Nakano H, Ishii N, Hashimoto T, Sawamura D
Case Reports in Dermatolgoy 2015.7
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Superficial epidermolytic ichthyosis caused by a novel KRT2 mutation.
Eijiro Akasaka, Satoko Minakawa, Daiki Rokunohe, Yuka Toyomaki, Yasushi Matsuzaki, Daisuke Sawamura, Hajime Nakano
Journal of dermatological science 79 ( 1 ) 86 - 88 2015.7
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Two Japanese familial cases of punctate palmoplantar keratoderma caused by a novel AAGAB mutation, c.191_194delCAAA.
Eijiro Akasaka, Yuko Okawa, Hajime Nakano, Noriko Takiyoshi, Daiki Rokunohe, Yuka Toyomaki, Daisuke Sawamura, Hirohiko Sueki
Journal of dermatological science 78 ( 2 ) 156 - 158 2015.5
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Diaminodiphenyl Sulfone-Induced Hemolytic Anemia and Alopecia in a Case of Linear IgA Bullous Dermatosis.
Akasaka E, Kayo SJ, Nakano H, Ishii N, Hashimoto T, Sawamura D
Case reports in dermatology 7 ( 2 ) 183 - 6 2015.5
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Two Japanese familial cases of punctate palmoplantar keratoderma caused by a novel AAGAB mutation, c.191_194delCAAA.
Akasaka E, Okawa Y, Nakano H, Takiyoshi N, Rokunohe D, Toyomaki Y, Sawamura D, Sueki H
Journal of dermatological science 78 ( 2 ) 156 - 8 2015.5
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Elderly-Onset Generalized Pustular Psoriasis without a Previous History of Psoriasis Vulgaris.
Aizu T, Matsui A, Takiyoshi N, Akasaka E, Kaneko T, Nakano H, Sugiura K, Akiyama M, Sawamura D
Case reports in dermatology 7 ( 2 ) 187 - 93 2015.5
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Anti-laminin γ1 pemphigoid associated with ulcerative colitis and psoriasis vulgaris showing autoantibodies to laminin γ1, type XVII collagen and laminin-332.
Eijiro Akasaka, Hajime Nakano, Ayumi Korekawa, Tomohisa Fukui, Takahide Kaneko, Hiroshi Koga, Takashi Hashimoto, Daisuke Sawamura
European journal of dermatology : EJD 25 ( 2 ) 198 - 199 2015.4
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Severe scoliosis associated with the WNT10A mutation.
Hanako Koguchi-Yoshioka, Mari Wataya-Kaneda, Hajime Nakano, Atsushi Tanemura, Eijiro Akasaka, Daisuke Sawamura, Ichiro Katayama
The Journal of dermatology 42 ( 3 ) 322 - 323 2015.3
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Case of oculocutaneous albinism complicated with squamous cell carcinoma, Bowen's disease and actinic keratosis.
Satoko Minakawa, Takahide Kaneko, Yasushi Matsuzaki, Eijiro Akasaka, Hiroki Mizukami, Yuko Abe, Yutaka Hozumi, Tamio Suzuki, Yoshihiko Mitsuhashi, Daisuke Sawamura
The Journal of dermatology 41 ( 9 ) 863 - 864 2014.9
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Mutational analysis on 16 Japanese population cases with epidermolysis bullosa simplex.
Satoko Minakawa, Hajime Nakano, Koji Nakajima, Yasushi Matsuzaki, Noriko Takiyoshi, Eijiro Akasaka, Daiki Rokunohe, Daisuke Sawamura
Journal of dermatological science 72 ( 3 ) 330 - 332 2013.12
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プロテインＣ活性低下がみられた下腿潰瘍．
赤坂英二郎、北村英夫、原田 研、三上英樹
皮膚病診療 2012.11
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Multiple aplasia cutis congenita lesions located along Blaschko's lines in a patient with tetralogy of Fallot-A.
Daiki Rokunohe, Eijiro Akasaka, Akiko Rokunohe, Takahide Kaneko, Yasushi Matsuzaki, Noriko Takiyoshi, Takayuki Aizu, Hajime Nakano, Daisuke Sawamura
Journal of dermatological case reports 6 ( 2 ) 40 - 42 2012.6
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Buschke-Ollendorff syndrome associated with hypertrophic scar formation: a possible role for LEMD3 mutation.
Korekawa A, Nakano H, Toyomaki Y, Takiyoshi N, Rokunohe D, Akasaka E, Nakajima K, Sawamura D.
Br J Dermatol 2012.4
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Multiple aplasia cutis congenita located along Blaschko's lines in a tetralogy of Fallot-A patient.
Rokunohe D, Akasaka E, Rokunohe A, Kaneko T, Matsuzaki Y, Takiyoshi N, Aizu T, Nakano H, Sawamura D.
J Dermtol Case Rep 2012.4
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Spindle Cell Hemangioma and Decorin Expression.
Rokunohe D, Takeda H, Kaneko T, Aizu T, Akasaka E, Matsuzaki Y, Nakano H, Sawamura D.
J Cos Dermatol Sci 2012.4
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びまん性および限局性の過角化を呈したケラチン6c遺伝子変異による掌蹠角化症．
赤坂英二郎、中野 創、豊巻由香、滝吉典子、六戸大樹、西川陽平、是川あゆ美、澤村大輔、中野あおい、三橋善比古.
第26回角化症研究会記録集 2012.4
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Characterization of retinoic acid-inducible gene-I (RIG-I) expression corresponding to viral infection and UVB in human keratinocytes.
Kimura K, Matsuzaki Y, Nishikawa Y, Kitamura H, Akasaka E, Rokunohe D, Nakano H, Imaizumi T, Satoh K, Sawamura D
Journal of dermatological science 66 ( 1 ) 64 - 70 2012.4
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Normolipidaemic xanthomatosis with systemic involvement of the skin, bone and pharynx.
Akasaka E, Matsuzaki Y, Kimura K, Ikenaga S, Takeuchi S, Nakano H, Sawamura D
Clin Exp Dermatol 2012.3
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Characterization of retinoic acid-inducible gene-I (RIG-I) expression corresponding to viral infection and UVB in human keratinocytes.
Kimura K, Matsuzaki Y, Nishikawa Y, Kitamura H, Akasaka E, Rokunohe D, Nakano H, Imaizumi T, Satoh K, Sawamura D
J Dermatol Sci 2012.1
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Diffuse and focal palmoplantar keratoderma can be caused by a keratin 6c mutation.
Akasaka E, Nakano H, Nakano A, Toyomaki Y, Takiyoshi N, Rokunohe D, Nishikawa Y, Korekawa A, Matsuzaki Y, Mitsuhashi Y, Sawamura D.
Br J Dermatol 2011.12
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V?rner type palmoplantar keratoderma: novel KRT9 mutation associated with knuckle pad-like lesions and recurrent mutation causing digital mutilation.
Umegaki N, Nakano H, Tamai K, Mitsuhashi Y, Akasaka E, Sawamura D, Katayama I.
Br J Dermatol 2011.3
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プロテインＣ活性低下を伴った静脈うっ滞性下腿潰瘍の１例．
赤坂英二郎、北村英夫、原田 研、三上英樹、河津 聡、野村亜南、矢嶋信久、黒滝日出一.
青県病誌 2011.1
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The interaction of photoprotective effects between keratinocytes and melanocytes via endothelin-1/stem cell factor signalings
Akasaka Eijiro, Nakano Hajime, Sato-Jin Kayo, Kimura Kazuyuki, Rokunohe Daiki, Imokawa Genji, Sawamura Daisuke
Hirosaki Medical Journal 62 ( 2 ) 138 - 143 2011
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Ultraviolet B irradiation inhibits retinoic acid-inducible gene-I expression in human keratinocytes.
Kimura Kazuyuki, Matsuzaki Yasushi, Kitamura Hideo, Akasaka Eijiro, Rokunohe Daiki, Nakano Hajime, Imaizumi Tadaatsu, Satoh Kei, Sawamura Daisuke
Hirosaki Medical Journal 62 ( 1 ) 1 - 6 2011
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Buschke-ollendorff syndrome pathogenetic mutation in an intron/exon boundary of the <i>LEMD3</i> gene
Korekawa Ayumi, Nakano Hajime, Rokunohe Daiki, Akasaka Eijiro, Nakajima Koji, Toyomaki Yuka, Sawamura Daisuke
Hirosaki Medical Journal 62 ( 2 ) 117 - 121 2011
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Raf kinase inhibitor protein expression correlates with differentiation but not with ERK phosphorylation in cutaneous squamous cell carcinoma.
Rokunohe D, Nakano H, Akasaka E, Kimura K, Takiyoshi N, Nakajima K, Aizu T, Kaneko T, Matsuzaki Y, Tsuchida S, Sawamura D.
J Dermatol Sci 2010.12
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Relation between the expression levels of the POU transcription factors Skn-1a and Skn-1n and keratinocyte differentiation.
Takemoto H, Tamai K, Akasaka E, Rokunohe D, Takiyoshi N, Umegaki N, Nakajima K, Aizu T, Kaneko T, Nakano H, Sawamura D
Journal of dermatological science 60 ( 3 ) 203 - 5 2010.12
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Leukemia cutis is an early sign of blast transformation that may mimic a common skin disease: sycosis-like eruptions in chronic myelomonocytic leukemia.
Takeuchi S, Akasaka E, Rokunohe D, Kayo SJ, Matsuzaki Y, Ooshima H, Nakano H, Sawamura D
The Journal of dermatology 37 ( 10 ) 916 - 8 2010.10
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Multiple eruptive dermatofibromas associated with Hashimoto's thyroiditis and myasthenia gravis.
Kimura Y, Kaneko T, Akasaka E, Nakajima K, Aizu T, Nakano H, Sawamura D.
EUR J Dermatol 2010.8
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Linear immunoglobulin A bullous dermatosis possibly induced by mefenamic acid
JIN Kayo, NAKANO Hajime, AKASAKA Eijiro, ROKUNOHE Daiki, MINAGAWA Satoko, ISHII Norito, HASHIMOTO Takashi, SAWAMURA Daisuke
Journal of dermatology 37 ( 3 ) 269 - 271 2010.3
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Linear IgA bullous dermatosis possibly induced by mefenamic acid.
Sato-Jin K, Nakano H, Akasaka E, Rokunohe D, Minagawa S, Ishii N, Hashimoto T, Sawamura D.
J Dermatol 2010.3
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Linear immunoglobulin A bullous dermatosis possibly induced by mefenamic acid.
Jin K, Nakano H, Akasaka E, Rokunohe D, Minakawa S, Ishii N, Hashimoto T, Sawamura D
The Journal of dermatology 37 ( 3 ) 269 - 71 2010.3
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A linear basal cell carcinoma undergoing spontaneous regression.
Takiyoshi N, Nakano H, Kaneko T, Aizu T, Nakajima K, Kimura K, Akasaka E, Rokunohe D, Nishizawa A, Kusumi T,* Sawamura D.
Clin Exp Dermatol 2009.10
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Novel and recurrent nonsense mutation of the SLC39A4 gene in Japanese patients with acrodermatitis enteropathica.
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.
Br J Dermatol 2009.7
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Multiple desmoplastic trichoepitheliomas with ossification and cholesterol deposition.
Takiyoshi N, Nakano H, Kaneko T, Aizu T, Nakajima K, Akasaka E, Rokunohe D, Sawamura D
Clin Exp Dermatol 2009.5
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Disseminated lupus vulgaris diagnosed more than 63 years after onset due to its initial misdiagnosis as a port-wine stain.
Takeuchi S, Nakano H, Rokunohe D, Akasaka E, Nishizawa A, Matsuzaki Y, Sawamura D.
Clin Exp Dermatol 2009.4
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An eclipse in the subungual space: a diagnostic sign for a subungual epidermal cyst?
Takiyoshi N, Nakano H, Matsuzaki Y, Aizu T, Kaneko T, Rokunohe D, Akasaka E, Jin K, Sawamura D, Ohara K
Br J Dermatol 2009.4
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Novel p.M1T and recurrent p.G301S mutations in cathepsin C in a Japanese patient with Papillon-Lef?vre syndrome: implications for understanding the genotype/phenotype relationship.
Ochiai T, Nakano H, Rokunohe D, Akasaka E, Toyomaki Y, Mitsuhashi Y, Sawamura D.
J Dermatol Sci 2009.4
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A novel homozygous missense mutation in the fatty aldehyde dehydrogenase gene causes Sjogren-Larsson syndrome
NAKANO Hajime, AKASAKA Eijiro, ROKUNOHE Daiki, YOKOYAMA Shohei, TOYOMAKI Yuka, UMEGAKI Noriko, MITSUHASHI Yoshihiko, SAWAMURA Daisuke
Journal of dermatological science 52 ( 2 ) 136 - 138 2008.11
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A novel homozygous missense mutation in the fatty aldehyde dehydrogenase gene causes Sjögren-Larsson syndrome.
Nakano H, Akasaka E, Rokunohe D, Yokoyama S, Toyomaki Y, Umegaki N, Mitsuhashi Y, Sawamura D
Journal of dermatological science 52 ( 2 ) 136 - 8 2008.11
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Epistatic connections between microphthalmia-associated transcription factor and endothelin signaling in Waardenburg syndrome and other pigmentary disorders.
Sato-Jin K, Nishimura EK, Akasaka E, Huber W, Nakano H, Miller A, Du J, Wu M, Hanada K, Sawamura D, Fisher DE, Imokawa G
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 22 ( 4 ) 1155 - 68 2008.4