Search Results - Naotomo Kambe
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1
Hereditary angioedema with a novel mutation, c.1481G>C, in the SERPING1 gene by Riko Takimoto‐Ito, Naotomo Kambe, Kazushi Izawa, Takahiro Yasumi, Kenji Kabashima
Published 2021Call Number: Loading…Connect to this object online.
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2
Dermoscopy of keratosis follicularis squamosa by Michiyo Nakano, Naotomo Kambe, Takashi Satou, Yaei Togawa, Noriaki Kamada, Hiroyuki Matsue
Published 2011Call Number: Loading…Connect to this object online.
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3
Spectrum of Genetic Autoinflammatory Diseases Presenting with Cutaneous Symptoms by Hanna Bonnekoh, Monique Butze, Tilmann Kallinich, Naotomo Kambe, Georgios Kokolakis, Karoline Krause
Published 2020Call Number: Loading…Connect to this object online.
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4
<i>NOD</i>2 Mutation-Associated Case with Blau Syndrome Triggered by BCG Vaccination by Akiko Arakawa, Naotomo Kambe, Ryuta Nishikomori, Akiyo Tanabe, Masamichi Ueda, Chikako Nishigori, Yoshiki Miyachi, Nobuo Kanazawa
Published 2021Call Number: Loading…Connect to this object online.
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5
Sustained Surface ICAM-1 Expression and Transient PDGF-B Production by Phorbol Myristate Acetate-Activated THP-1 Cells Harboring Blau Syndrome-Associated <em>NOD2</em> Mutations by Mizuho Nishiyama, Hong-jin Li, Ikuo Okafuji, Akihiko Fujisawa, Mizue Ehara, Naotomo Kambe, Fukumi Furukawa, Nobuo Kanazawa
Published 2021Call Number: Loading…Connect to this object online.
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6
Panniculitis in dermatomyositis: Two cases with antitranscriptional intermediary factor‐1 antibody as myositis‐specific antibody and review of the literature by Kaori Takezawa, Ikuko Ueda‐Hayakawa, Akihiro Tanaka, Yonsu Son, Fumikazu Yamazaki, Naotomo Kambe, Hiroyuki Okamoto, Manabu Fujimoto
Published 2022Call Number: Loading…Connect to this object online.
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7
Incomplete penetrance of NOD2 C483W mutation underlining Blau syndrome by Shao-Yu Chang, Naotomo Kambe, Wen-Lang Fan, Jing-Long Huang, Wen-I Lee, Chao-Yi Wu
Published 2022Call Number: Loading…Connect to this object online.
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