The hands in health and disease of individuals with filaggrin loss-of-function mutations: clinical reflections on the hand eczema phenotype
Author:
Publisher
Wiley
Subject
Dermatology,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0536.2012.02130.x/fullpdf
Reference21 articles.
1. Filaggrin mutations associated with skin and allergic diseases.;Irvine;N Engl J Med,2011
2. Filaggrin null mutations increase the risk and persistence of hand eczema in subjects with atopic dermatitis: results from a general population study.;Thyssen;Br J Dermatol,2010
3. Filaggrin genotype in ichthyosis vulgaris predicts abnormalities in epidermal structure and function.;Gruber;Am J Pathol,2011
4. Filaggrin deficiency confers a paracellular barrier abnormality that reduces inflammatory thresholds to irritants and haptens.;Scharschmidt;J Allergy Clin Immunol,2009
5. Filaggrin loss-of-function mutations are associated with early-onset eczema, eczema severity and transepidermal water loss at 3 months of age.;Flohr;Br J Dermatol,2010
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