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Showing results 1 to 6 of 6
TypeAuthor(s)TitleOther TitlesCitationCitation(alt)Issue Date
article (author version)Natsuga, Ken; Sawamura, Daisuke; Homma, Erina; Nomura, Toshifumi; Abe, Masataka; Muramatsu, Ryuichi; Mochizuki, Toshio; Koike, Takao; Shimizu, HiroshiAmicrobial pustulosis associated with IgA nephropathy and Sjögren's syndrome-Journal of the American Academy of Dermatology-Sep-2007
article (author version)Nagasaki, Akari; Nishie, Wataru; Sato, Kozo; Oba, Ikuko; Noguchi, Emiko; Akitsu, Hideki; Sawamura, Daisuke; Shimizu, HiroshiClinical and genetic analysis of Fabry disease : report of six cases including three heterozygous females-Journal of Dermatological Science-Oct-2008
article (author version)Sawamura, Daisuke; Sato-Matsumura, Kazuko; Shibata, Satoko; Tashiro, Akari; Furue, Masutaka; Goto, Maki; Sakai, Kaori; Akiyama, Masashi; Nakamura, Hideki; Shimizu, HiroshiCOL7A1 mutation G2037E causes epidermal retention of type VII collagen-Journal of Human Genetics-May-2006
article (author version)Akiyama, Masashi; Sakai, Kaori; Sugiyama-Nakagiri, Yoriko; Yamanaka, Yasuko; McMillan, James R; Sawamura, Daisuke; Niizeki, Hironori; Miyagawa, Sachiko; Shimizu, HiroshiCompound heterozygous mutations including a de novo missense mutation in ABCA12 led to a case of harlequin ichthyosis with moderate clinical severity-Journal of Investigative Dermatology-Jul-2006
article (author version)Sawamura, Daisuke; Goto, Maki; Yasukawa, Kana; Sato-Matsumura, Kazuko; Nakamura, Hideki; Ito, Kei; Nakamura, Hiroyuki; Tomita, Yuki; Shimizu, HiroshiGenetic studies of 20 Japanese families of dystrophic epidermolysis bullosa-Journal of Human Genetics-Oct-2005
article (author version)Tsubota, Akiko; Akiyama, Masashi; Sakai, Kaori; Goto, Maki; Nomura, Yukiko; Ando, Satomi; Abe, Masataka; Sawamura, Daisuke; Shimizu, HiroshiKeratin 1 Gene Mutation Detected in Epidermal Nevus with Epidermolytic Hyperkeratosis-Journal of Investigative Dermatology-Jun-2007
Showing results 1 to 6 of 6

 

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