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Page 1
Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2.
Fischer J, Degenhardt F, Hofmann A, Redler S, Basmanav FB, Heilmann-Heimbach S, Hanneken S, Giehl KA, Wolff H, Moebus S, Kruse R, Lutz G, Blaumeiser B, Böhm M, Garcia Bartels N, Blume-Peytavi U, Petukhova L, Christiano AM, Nöthen MM, Betz RC. Fischer J, et al. Exp Dermatol. 2017 Jun;26(6):536-541. doi: 10.1111/exd.13123. Epub 2017 Mar 23. Exp Dermatol. 2017. PMID: 27306922
Hay-Wells syndrome in a child with mutation in the TP73L gene.
Garcia Bartels N, Neumann LM, Mleczko A, Rubach K, Peters H, Rossi R, Sterry W, Blume-Peytavi U. Garcia Bartels N, et al. J Dtsch Dermatol Ges. 2007 Oct;5(10):919-23. doi: 10.1111/j.1610-0387.2007.06379.x. J Dtsch Dermatol Ges. 2007. PMID: 17910675 English, German.
Morphometry of human terminal and vellus hair follicles.
Vogt A, Hadam S, Heiderhoff M, Audring H, Lademann J, Sterry W, Blume-Peytavi U. Vogt A, et al. Exp Dermatol. 2007 Nov;16(11):946-50. doi: 10.1111/j.1600-0625.2007.00602.x. Exp Dermatol. 2007. PMID: 17927578
[Hair loss or pseudo hair loss].
Mleczko A, Garcia Bartels N, Kahl C, Blume-Peytavi U. Mleczko A, et al. J Dtsch Dermatol Ges. 2007 Nov;5(11):1031-3. doi: 10.1111/j.1610-0387.2007.06393.x. J Dtsch Dermatol Ges. 2007. PMID: 17976145 German. No abstract available.
365 results