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Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia.
Numata S, Teye K, Krol RP, Karashima T, Fukuda S, Matsuda M, Ishii N, Furumura M, Ohata C, Saminathan SD, Ariffin R, Pramono ZA, Leong KF, Hamada T, Hashimoto T. Numata S, et al. Among authors: krol rp. J Dermatol Sci. 2015 Apr;78(1):82-5. doi: 10.1016/j.jdermsci.2015.02.006. Epub 2015 Feb 19. J Dermatol Sci. 2015. PMID: 25766764 No abstract available.
A founder deletion of corneodesmosin gene is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases.
Teye K, Suga Y, Numata S, Soejima M, Ishii N, Krol RP, Ohata C, Matsuda M, Honma M, Ishida-Yamamoto A, Hamada T, Koda Y, Hashimoto T. Teye K, et al. Among authors: krol rp. J Dermatol Sci. 2016 May;82(2):134-7. doi: 10.1016/j.jdermsci.2016.01.012. Epub 2016 Jan 29. J Dermatol Sci. 2016. PMID: 26867961 No abstract available.
Immunological and statistical studies of anti-BP180 antibodies in paraneoplastic pemphigus.
Tsuchisaka A, Kawano H, Yasukochi A, Teye K, Ishii N, Koga H, Sogame R, Ohzono A, Krol RP, Kawakami T, Furumura M, Ohata C, Li X, Hashimoto T. Tsuchisaka A, et al. Among authors: krol rp. J Invest Dermatol. 2014 Aug;134(8):2283-2287. doi: 10.1038/jid.2014.151. Epub 2014 Mar 31. J Invest Dermatol. 2014. PMID: 24658507 Free article. No abstract available.
Anti-early endosome antigen 1 autoantibodies were detected in a pemphigus-like patient but not in the majority of pemphigus diseases.
Nishikawa R, Takahashi H, Matsuda M, Imaoka K, Ogawa M, Teye K, Tsuchisaka A, Koga H, Komorowski L, Probst C, Hachiya T, Fritzler MJ, Ishii N, Ohata C, Furumura M, Krol RP, Muro Y, Morita E, Hashimoto T. Nishikawa R, et al. Among authors: krol rp. Exp Dermatol. 2016 May;25(5):368-74. doi: 10.1111/exd.12981. Exp Dermatol. 2016. PMID: 26909655
18 results