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See Latest ArticlesFGFR3 and PIK3CA mutations in stucco keratosis and dermatosis papulosa nigra
British Journal of Dermatology, 10/26/09
Hafner C et al. – The results indicate that FGFR3 and PIK3CA mutations are involved in the pathogenesis of STK and DPN. The molecular genetic findings furthermore support the concept that both skin lesions are specific variants of seborrhoeic keratosis, sharing a common genetic background.
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Efficacy of a Single Educative Intervention in Patients with Chronic Plaque Psoriasis
Dermatology, 12/02/09
Efficacy and safety of long-term mycophenolate sodium therapy in pemphigus vulgaris
Journal of the European Academy of Dermatology and Venereology, 12/02/09
Different therapeutic modalities for treatment of melasma
Journal of Cosmetic Dermatology, 12/02/09
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