Occupational ionizing radiation-induced skin injury among orthopedic surgeons: A clinical survey von Asari, Toru, Rokunohe, Daiki, Sasaki, Eiji, Kaneko, Takahide, Kumagai, Gentaro, Wada, Kanichiro, Tanaka, Sunao, Sawamura, Daisuke, Ishibashi, Yasuyuki

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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 coproporphyrin... von Fukui, Tomohisa, Akasaka, Eijiro, Rokunohe, Daiki, Matsuzaki, Yasushi, Sawamura, Daisuke, Kabashima, Kenji, Nakano, Hajime

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The first Japanese case of familial porphyria cutanea tarda diagnosed by a UROD mutation von Matsui, Akinobu, Akasaka, Eijiro, Rokunohe, Daiki, Matsuzaki, Yasushi, Sawamura, Daisuke, Nakano, Hajime

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Rubinstein-Taybi syndrome with multiple pilomatricomas: The first case diagnosed by CREBBP mutation analysis von Rokunohe, Daiki, Nakano, Hajime, Akasaka, Eijiro, Toyomaki, Yuka, Sawamura, Daisuke

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Significance of IL36RN mutation analyses in the management of impetigo herpetiformis: A case report and review of published cases von Yoshikawa, Miyuki, Rokunohe, Daiki, Kimura, Atsuko, Takahashi, Mika, Korekawa, Ayumi, Nakajima, Koji, Nakano, Hajime, Yokoyama, Minako, Tanaka, Kanji, Yokoyama, Yoshihito, Sawamura, Daisuke

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Autoimmune hemolytic anemia during long‐term administration of nivolumab for metastatic melanoma von Nakajima, Koji, Korekawa, Ayumi, Rokunohe, Daiki, Nakano, Hajime, Sawamura, Daisuke

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Immunosuppressive effect of adipose-derived stromal cells on imiquimod-induced psoriasis in mice von Rokunohe, Akiko, Matsuzaki, Yasushi, Rokunohe, Daiki, Sakuraba, Yusuke, Fukui, Tomohisa, Nakano, Hajime, Sawamura, Daisuke

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Two Japanese familial cases of punctate palmoplantar keratoderma caused by a novel AAGAB mutation, c.191_194delCAAA von Akasaka, Eijiro, Okawa, Yuko, Nakano, Hajime, Takiyoshi, Noriko, Rokunohe, Daiki, Toyomaki, Yuka, Sawamura, Daisuke, Sueki, Hirohiko

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Juvenile temporal arteritis with eosinophilia associated with systemic sclerosis von Matsui, Akinobu, Kaneko, Takahide, Takiyoshi, Noriko, Rokunohe, Daiki, Nakano, Hajime, Sawamura, Daisuke

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Superficial epidermolytic ichthyosis caused by a novel KRT2 mutation von Akasaka, Eijiro, Minakawa, Satoko, Rokunohe, Daiki, Toyomaki, Yuka, Matsuzaki, Yasushi, Sawamura, Daisuke, Nakano, Hajime

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Characterization of retinoic acid-inducible gene-I (RIG-I) expression corresponding to viral infection and UVB in human keratinocytes von Kimura, Kazuyuki, Matsuzaki, Yasushi, Nishikawa, Yohei, Kitamura, Hideo, Akasaka, Eijiro, Rokunohe, Daiki, Nakano, Hajime, Imaizumi, Tadaatsu, Satoh, Kei, Sawamura, Daisuke

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Relation between the expression levels of the POU transcription factors Skn-1a and Skn-1n and keratinocyte differentiation von Takemoto, Hironobu, Tamai, Katsuto, Akasaka, Eijiro, Rokunohe, Daiki, Takiyoshi, Noriko, Umegaki, Noriko, Nakajima, Koji, Aizu, Takayuki, Kaneko, Takahide, Nakano, Hajime, Sawamura, Daisuke

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Mutational analysis on 16 Japanese population cases with epidermolysis bullosa simplex von Minakawa, Satoko, Nakano, Hajime, Nakajima, Koji, Matsuzaki, Yasushi, Takiyoshi, Noriko, Akasaka, Eijiro, Rokunohe, Daiki, Sawamura, Daisuke

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Primary Amelanotic Rhabdoid Melanoma: A Case Report with Review of the Literature von Kaneko, Takahide, Korekawa, Ayumi, Akasaka, Eijiro, Rokunohe, Daiki, Nakano, Hajime, Sawamura, Daisuke

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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 von Akasaka, Eijiro, Rokunohe, Daiki, Nakano, Hajime, Yamatani, Shingo, Sawamura, Daisuke

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Deciphering UV‐induced DNA Damage Responses to Prevent and Treat Skin Cancer von Lee, Jihoon W., Ratnakumar, Kajan, Hung, Kai‐Feng, Rokunohe, Daiki, Kawasumi, Masaoki

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Raf kinase inhibitor protein expression correlates with differentiation but not with ERK phosphorylation in cutaneous squamous cell carcinoma von Rokunohe, Daiki, Nakano, Hajime, Akasaka, Eijiro, Kimura, Kazuyuki, Takiyoshi, Noriko, Nakajima, Koji, Aizu, Takayuki, Kaneko, Takahide, Matsuzaki, Yasushi, Tsuchida, Shigeki, Sawamura, Daisuke

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Novel p.M1T and recurrent p.G301S mutations in cathepsin C in a Japanese patient with Papillon-Lefèvre syndrome: Implications for understanding the genotype/phenotype relationship von Ochiai, Toyoko, Nakano, Hajime, Rokunohe, Daiki, Akasaka, Eijiro, Toyomaki, Yuka, Mitsuhashi, Yoshihiko, Sawamura, Daisuke

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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 von TAKEUCHI, Sonoko, AKASAKA, Eijiro, ROKUNOHE, Daiki, KAYO, Sato-Jin, MATSUZAKI, Yasushi, OOSHIMA, Hanae, NAKANO, Hajime, SAWAMURA, Daisuke

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Linear immunoglobulin A bullous dermatosis possibly induced by mefenamic acid von JIN, Kayo, NAKANO, Hajime, AKASAKA, Eijiro, ROKUNOHE, Daiki, MINAGAWA, Satoko, ISHII, Norito, HASHIMOTO, Takashi, SAWAMURA, Daisuke

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