Erythrokeratodermia variabilis

Known as: EKVP, Erythrokeratodermia Figurata, Congenital Familial, in Plaqus, PSEK 
An autosomal dominant skin disease characterized by transient and variable noninflammatory ERYTHEMA and hyperkeratosis. It has been associated with… (More)
National Institutes of Health

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AcanthosisAutosomal dominant inheritanceCongenital ichthyosisConnexins
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ERYTHROKERATODERMIA VARIABILIS 3 (disorder)

Papers overview

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Review
2016
Review
2016
Erythrokeratodermia variabilis et progressiva.
Erythrokeratodermia variabilis et progressiva (EKVP) is a rare inherited skin disease characterized by fixed hyperkeratotic… (More)
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2013
2013
Erythrokeratodermia variabilis: Two case reports
Erythrokeratodermia variabilis (EKV) is a rare heterogeneous skin disorder. The classical EKV first described by Mendes da Costa… (More)
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Highly Cited
2008
Highly Cited
2008
Genes of cyanobacterial origin in plant nuclear genomes point to a heterocyst-forming plastid ancestor.
Plastids are descended from a cyanobacterial symbiosis which occurred over 1.2 billion years ago. During the course of… (More)
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Highly Cited
2007
Highly Cited
2007
Tradeoffs and Optimization in Analog CMOS Design
  • Dave Binkley
  • 14th International Conference on Mixed Design of…
  • 2007
The selection of drain current, inversion coefficient, and channel length for each MOS device in an analog circuit results in… (More)
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Highly Cited
2004
Highly Cited
2004
Social-Ecological Transformation for Ecosystem Management : the Development of Adaptive Co-management of a Wetland Landscape in Southern Sweden
We analyze the emergence of an adaptive co-management system for wetland landscape governance in southern Sweden, a process where… (More)
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2003
2003
Genetic heterogeneity in erythrokeratodermia variabilis: novel mutations in the connexin gene GJB4 (Cx30.3) and genotype-phenotype correlations.
Erythrokeratodermia variabilis is an autosomal dominant genodermatosis characterized by persistent plaque-like or generalized… (More)
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2003
2003
Molecular interaction of connexin 30.3 and connexin 31 suggests a dominant-negative mechanism associated with erythrokeratodermia variabilis.
Connexins are homologous four-transmembrane-domain proteins and major components of gap junctions. We recently identified… (More)
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2003
2003
Erythrokeratodermia variabilis.
A 47-year-old woman presented with both transient, figurate, erythematous patches and fixed, hyperkeratotic plaques on the upper… (More)
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Highly Cited
1999
Highly Cited
1999
Phylogeny and polyphasic taxonomy of Caulobacter species. Proposal of Maricaulis gen. nov. with Maricaulis maris (Poindexter) comb. nov. as the type species, and emended description of the genera…
The genus Caulobacter is composed of prosthecate bacteria often specialized for oligotrophic environments. The taxonomy of… (More)
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Highly Cited
1998
Highly Cited
1998
Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis
Erythrokeratodermia variabilis (EKV, OMIM 133200) is an autosomal dominant genodermatosis with considerable intra- and… (More)
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