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Ichthyosis Vulgaris

Known as: Ichthyosis Vulgaris [Disease/Finding], Ichthyosis Vulgaris, Dominant, Ichthyosis Simplex 
Most common form of ICHTHYOSIS characterized by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an… Expand
National Institutes of Health

Papers overview

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Highly Cited
2011
Highly Cited
2011
Although it is widely accepted that filaggrin (FLG) deficiency contributes to an abnormal barrier function in ichthyosis vulgaris… Expand
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Review
2010
Review
2010
  • Y. Tokura
  • Journal of dermatological science
  • 2010
  • Corpus ID: 29664778
Atopic dermatitis (AD) can be categorized into the extrinsic and intrinsic types. Extrinsic or allergic AD shows high total serum… Expand
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Review
2010
Review
2010
  • M. Akiyama
  • The British journal of dermatology
  • 2010
  • Corpus ID: 28311060
Filaggrin is a key protein involved in skin barrier function. Mutations in the gene encoding filaggrin (FLG) have been identified… Expand
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Highly Cited
2009
Highly Cited
2009
Recently, loss-of-function mutations in FLG, the human gene encoding profilaggrin and filaggrin, have been identified as the… Expand
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Highly Cited
2008
Highly Cited
2008
Mutations in the gene encoding filaggrin (FLG) have been identified as the cause of ichthyosis vulgaris (IV) and shown to be… Expand
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Highly Cited
2007
Highly Cited
2007
We recently reported two common filaggrin (FLG) null mutations that cause ichthyosis vulgaris and predispose to eczema and… Expand
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Highly Cited
2007
Highly Cited
2007
BACKGROUND Filaggrin is a key protein involved in skin barrier function. Recently, mutations in the filaggrin gene, FLG, were… Expand
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Highly Cited
2006
Highly Cited
2006
BACKGROUND Atopic dermatitis (AD) is a chronic inflammatory skin disease with a strong genetic background. One of the… Expand
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Highly Cited
2006
Highly Cited
2006
Mutations in the filament aggregating protein (filaggrin) gene have recently been identified as the cause of the common genetic… Expand
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Highly Cited
1985
Highly Cited
1985
Ichthyosis vulgaris is an autosomal dominant disorder of keratinization characterized histologically by absent or reduced… Expand
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