Author/Creator: Okamura, Ken - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Okamura, Ken

41. Rhododenol-induced leukoderma in a mouse model mimicking Japanese skin. Issue 1 (January 2016)

Authors:: Abe, Yuko; Okamura, Ken; Kawaguchi, Masakazu; Hozumi, Yutaka; Aoki, Hitomi; Kunisada, Takahiro; Ito, Shosuke; Wakamatsu, Kazumasa; Matsunaga, Kayoko; Suzuki, Tamio
Journal:: Journal of dermatological science
Issue:: Volume 81:Issue 1(2016:Jan.)
Page Start:: 35
Record Type:: Journal Article
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42. The effect of a topical vitamin D3 analog on repigmentation in mice with rhododendrol-induced leukoderma. Issue 2 (May 2022)

Authors:: Abe, Yuko; Okamura, Ken; Ito, Shosuke; Hozumi, Yutaka; Suzuki, Tamio
Journal:: Journal of dermatological science
Issue:: Volume 106:Issue 2(2022)
Page Start:: 127
Record Type:: Journal Article
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43. Ultrastructural study of dyschromatosis symmetrica hereditaria with widespread pigmentary eruption. Issue 7 (31st March 2017)

Authors:: Omura, Reina; Fukai, Kazuyoshi; Sugawara, Koji; Tsuruta, Daisuke; Okamura, Ken; Hozumi, Yutaka; Suzuki, Tamio
Journal:: Journal of dermatology
Issue:: Volume 44:Issue 7(2017)
Page Start:: e150
Record Type:: Journal Article
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44. Waardenburg syndrome type IIE in a Japanese patient caused by a novel missense mutation in the SOX10 gene. Issue 12 (14th September 2015)

Authors:: Okamura, Ken; Oiso, Naoki; Tamiya, Gen; Makino, Satoshi; Tsujioka, Daishi; Abe, Yuko; Kawaguchi, Masakazu; Hozumi, Yutaka; Shimomura, Yoshikazu; Suzuki, Tamio
Journal:: Journal of dermatology
Issue:: Volume 42:Issue 12(2015)
Page Start:: 1211
Record Type:: Journal Article
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45. Waardenburg syndrome type IIE in a Japanese patient caused by a novel non‐frame‐shift duplication mutation in the SOX10 gene. Issue 5 (23rd November 2017)

Authors:: Hemmi, Ami; Okamura, Ken; Tazawa, Ryushi; Abe, Yuko; Hayashi, Masahiro; Izumi, Shuji; Tohyama, Jun; Shimomura, Yutaka; Hozumi, Yutaka; Suzuki, Tamio
Journal:: Journal of dermatology
Issue:: Volume 45:Issue 5(2018)
Page Start:: e110
Record Type:: Journal Article
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46. Whole-exome sequencing confirmation of multiple MC1R variants associated with extensive freckles and red hair: Analysis of a Mongolian family. Issue 2 (November 2016)

Authors:: Araki, Yuta; Okamura, Ken; Munkhbat, Batmunkh; Tamiya, Gen; Erdene-Ochir, Bujin; Nemekhbaatar, Lkhasuren; Hozumi, Yutaka; Suzuki, Tamio
Journal:: Journal of dermatological science
Issue:: Volume 84:Issue 2(2016:Nov.)
Page Start:: 216
Record Type:: Journal Article
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