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The Journal of Investigative Dermatology|August 21, 2001
A mannose-binding receptor is expressed on human keratinocytes and mediates killing of Candida albicansG Szolnoky, Z Bata-Csörgö, A S Kenderessy, et al.
The British Journal of Dermatology|July 22, 2008
A 4-year follow-up study of atopic dermatitis therapy with 0.1% tacrolimus ointment in children and adult patientsS Reitamo, M Rustin, J Harper, et al.
The British Journal of Dermatology|September 11, 2008
Proactive disease management with 0.03% tacrolimus ointment for children with atopic dermatitis: results of a randomized, multicentre, comparative studyD Thaçi, S Reitamo, M A Gonzalez Ensenat, et al.
Allergy|January 14, 2015
Contact allergy induced by bisphenol A diglycidyl ether leachables from aluminium tubes for pharmaceutical useK Breuer, C Lipperheide, U Lipke, et al.
Advances in Experimental Medicine and Biology|December 22, 1999
Polymorphisms of the xenobiotic-metabolizing enzymes CYP1A1 and NAT-2 in systemic sclerosis and lupus erythematosusS von Schmiedeberg, E Fritsche, A C Rönnau, et al.
The British Journal of Dermatology|August 18, 2009
A randomized controlled trial of R-salbutamol for topical treatment of discoid lupus erythematosusG B E Jemec, S Ullman, M Goodfield, et al.
American Journal of Human Genetics|June 23, 1998
Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteriaR Kruse, A Rütten, C Lamberti, et al.
The British Journal of Dermatology|March 13, 2010
Systematic mutation screening of KRT5 supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos diseaseS Hanneken, A Rütten, S M Pasternack, et al.
The EMBO Journal|August 1, 1986
Mechanism of postsegregational killing by the hok gene product of the parB system of plasmid R1 and its homology with the relF gene product of the E. coli relB operonK Gerdes, F W Bech, S T Jørgensen, et al.
The British Journal of Dermatology|November 30, 2018
Association of pyrin mutations and autoinflammation with complex phenotype hidradenitis suppurativa: a case-control studyS Vural, M Gündoğdu, E Gökpınar İli, et al.
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