Dermatology

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Dyschromatosis universalis hereditaria in a young Nigerian female
International Journal of Dermatology, 06/23/09

Yusuf SM et al. - Dyschromatosis universalis hereditaria (DUH) is a clinically heterogeneous disorder that shows generalized mottled pigmentation. It occurs most commonly in Japanese persons, with sporadic reports from South Africa, India, and Iraq. Histopathology reveals a variable degree of pigmentary incontinence. Although the precise etiology of this disorder is not yet known, the clinicopathological findings implicate an inherent abnormality of melanosomes or melanin processing.

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Basic fibroblast growth factor stimulates the proliferation of human dermal fibroblasts via the ERK1/2 and JNK pathways
British Journal of Dermatology, 12/10/09

Analysis of family history of palmoplantar hyperhidrosis in Japan
Journal of Dermatology, 12/08/09

Evidence for a Founder Mutation in the Cathepsin C Gene in Three Families with Papillon-Lefevre Syndrome
Dermatology, 12/08/09

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Idiopathic Chilblains
American Journal of Medicine, 12/10/09

Randomized, Placebo-Controlled Study of a New Botulinum Toxin Type A for Treatment of Glabellar Lines: Efficacy and Safety
Dermatologic Surgery, 12/10/09

Basic fibroblast growth factor stimulates the proliferation of human dermal fibroblasts via the ERK1/2 and JNK pathways
British Journal of Dermatology, 12/10/09

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