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Familial Primary Localized Cutaneous Amyloidosis in Brazil
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Sakuma TH et al. - Familial PLCA shows autosomal dominant inheritance, but there is clinical and genetic heterogeneity and variable clinical penetrance. Demonstration of mutations in the OSMR gene provides new insight into mechanisms of itch and apoptosis in human skin.
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Living skin equivalents constructed using human amnions as a matrix
Journal of Dermatological Science, 12/03/09
Telomeric DNA induces p53-dependent reactive oxygen species and protects against oxidative damage
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Today in Dermatopathology...keeping you current
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Physical Activity and Fatigue in Breast Cancer and Multiple Sclerosis: Psychosocial Mechanisms
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Pimecrolimus 1% cream, methylprednisolone aceponate 0.1% cream and metronidazole 0.75% gel in the treatment of seborrhoeic dermatitis: A randomized clinical study
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