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Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease.
Oji V, Eckl KM, Aufenvenne K, Nätebus M, Tarinski T, Ackermann K, Seller N, Metze D, Nürnberg G, Fölster-Holst R, Schäfer-Korting M, Hausser I, Traupe H, Hennies HC. Oji V, et al. Among authors: aufenvenne k. Am J Hum Genet. 2010 Aug 13;87(2):274-81. doi: 10.1016/j.ajhg.2010.07.005. Am J Hum Genet. 2010. PMID: 20691404 Free PMC article.
Ichthyosis vulgaris: novel FLG mutations in the German population and high presence of CD1a+ cells in the epidermis of the atopic subgroup.
Oji V, Seller N, Sandilands A, Gruber R, Gerss J, Hüffmeier U, Hamm H, Emmert S, Aufenvenne K, Metze D, Luger T, Loser K, Hausser I, Traupe H, McLean WH. Oji V, et al. Among authors: aufenvenne k. Br J Dermatol. 2009 Apr;160(4):771-81. doi: 10.1111/j.1365-2133.2008.08999.x. Epub 2009 Jan 13. Br J Dermatol. 2009. PMID: 19183181
Complete filaggrin deficiency in ichthyosis vulgaris is associated with only moderate changes in epidermal permeability barrier function profile.
Perusquía-Ortiz AM, Oji V, Sauerland MC, Tarinski T, Zaraeva I, Seller N, Metze D, Aufenvenne K, Hausser I, Traupe H. Perusquía-Ortiz AM, et al. Among authors: aufenvenne k. J Eur Acad Dermatol Venereol. 2013 Dec;27(12):1552-8. doi: 10.1111/jdv.12079. Epub 2013 Jan 7. J Eur Acad Dermatol Venereol. 2013. PMID: 23297869
17 results