Results 111 to 120 of about 281 (139)
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ACROKERATOSIS VERRUCIFORMIS OF HOPF WITH STEATOCYSTOMA MULTIPLEX AND HYPERTKOPHIC LICHEN PLANUS
British Journal of Dermatology, 1972SUMMARY.— The case is reported of a woman aged 50 with acrokeratosis verruciformis of Hopf. The patient's father and a sister were said to have similar lesions. The patient also had steatocystoma multiplmx in the presternal region and hypertrophic lichen planus over the elbows.
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Twenty Hopf-like bifurcations in piecewise-smooth dynamical systems
Physics Reports, 2022David J W Simpson
exaly
Acrokeratosis Verruciformis of Hopf: a localized variant.
Journal of drugs in dermatology : JDD, 2005Acrokeratosis Verruciformis of Hopf (AKV) is a rare autosomal dominant genodermatosis. It usually develops during early childhood affecting both sexes equally. Typically, the lesions are warty to convex, brownish to skin-colored papules on the dorsa of the hands and feet, forearms and legs.
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Acrokeratosis verruciformis of Hopf: dermoscopy approach in dark skin patients
Journal of the European Academy of Dermatology and Venereology, 2022J.M. Llamas‐Molina +5 more
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Acrokeratosis verruciformis of Hopf: Dermoscopic approach in lighter phototypes
Journal of the European Academy of Dermatology and Venereology, 2022openaire +2 more sources
Acrokeratosis verruciformis of Hopf: dermoscopic and histopathological study of two siblings
Clinical and Experimental Dermatology, 2021R. Genedy, A. Taha
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Chaos, Hopf bifurcation and control of a fractional-order delay financial system
Mathematics and Computers in Simulation, 2022He Ke
exaly