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Zeitschrift

Archives of Dermatological Research

Archives of Dermatological Research 2/2012

Ausgabe 2/2012

Inhaltsverzeichnis ( 10 Artikel )

01.03.2012 | Guideline | Ausgabe 2/2012

German S3-guidelines on the treatment of psoriasis vulgaris (short version)

A. Nast, W. H. Boehncke, U. Mrowietz, H. M. Ockenfels, S. Philipp, K. Reich, T. Rosenbach, A. Sammain, M. Schlaeger, M. Sebastian, W. Sterry, V. Streit, M. Augustin, R. Erdmann, J. Klaus, J. Koza, S. Müller, H. D. Orzechowski, S. Rosumeck, G. Schmid-Ott, T. Weberschock, B. Rzany

01.03.2012 | News & Views | Ausgabe 2/2012

Exploring the role of prolactin in psoriasis

Ewan A. Langan, Christopher E. M. Griffiths, Ralf Paus

01.03.2012 | Original Paper | Ausgabe 2/2012

Psoriasis increased the risk of diabetes: a meta-analysis

Juan Cheng, Dayu Kuai, Li Zhang, Xueqin Yang, Bing Qiu

01.03.2012 | Original Paper | Ausgabe 2/2012

The association of PASI scores with CRH-R1 expression in patients with psoriasis

Bengü Çevirgen Cemil, Filiz Canpolat, Demet Yılmazer, Fatma Eskioğlu, Murat Alper

01.03.2012 | Original Paper | Ausgabe 2/2012

Endothelial and axon reflex vasodilatation to acetylcholine in rosacea-affected skin

Peter D. Drummond, Daphne Su

01.03.2012 | Original Paper | Ausgabe 2/2012

A simple, noninvasive and efficient method for transdermal delivery of siRNA

Chang-Min Lin, Keng Huang, Yang Zeng, Xian-Cai Chen, Sen Wang, Yu Li

01.03.2012 | Original Paper | Ausgabe 2/2012

A putative in vitro organotypic model of molting with human skin explants

A. Peramo, S. E. Feinberg, C. L. Marcelo

01.03.2012 | Original Paper | Ausgabe 2/2012

Comparison of the spread of three botulinum toxin type A preparations

Martina Kerscher, Susanna Roll, Andreas Becker, Walter Wigger-Alberti

01.03.2012 | Original Paper | Ausgabe 2/2012

Detection and comparison of two types of ATP2C1 gene mutations in Chinese patients with Hailey–Hailey disease

Dingwei Zhang, Xiaoli Li, Shengxiang Xiao, Jia Huo, Shuang Wang, Pengjun Zhou

01.03.2012 | Original Paper | Ausgabe 2/2012

Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity

O. Messaoud, M. Ben Rekaya, H. Ouragini, S. Benfadhel, H. Azaiez, R. Kefi, N. Gouider-Khouja, I. Mokhtar, A. Amouri, M. S. Boubaker, M. Zghal, S. Abdelhak

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