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See Latest ArticlesAutosomal Dominant Epidermodysplasia Verruciformis Lacking a Known EVER1 or EVER2 Mutation
Pediatric Dermatology, 06/26/09
McDermott DF et al. - Epidermodysplasia verruciformis is a rare genodermatosis characterized by abnormal susceptibility to infection with specific human papillomavirus serotypes. Epidermodysplasia verruciformis is a genetically heterogeneous disease, and autosomal recessive and X-linked inheritance patterns have been reported. Nonsense mutations in the genes EVER1 and EVER2 have been identified in over 75% of cases.
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Usefulness of the CD63 basophil activation test in detecting Anisakis hypersensitivity in patients with chronic urticaria: diagnosis and follow-up
Clinical and Experimental Dermatology, 11/02/09
C-Kit (CD117) expression in classic Kaposis sarcoma
Clinical and Experimental Dermatology, 11/02/09
Repeated episodes of fixed eruption 3 months after discontinuing pegylated interferon-alpha-2b plus ribavirin combination therapy in a patient with chronic hepatitis C virus infection
Clinical and Experimental Dermatology, 10/16/09
Today in Derm Infectious Disease...keeping you current
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Erysipeloid: a review
Clinical and Experimental Dermatology, 09/18/09
A practical approach to using methotrexate
Dermatology in Practice, 10/09/09
Ulcerative leg nodules in a transplant recipient
Cleveland Clinic Journal of Medicine, 10/16/09
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