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… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1947-2018
0102019472017

Papers overview

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2011
2011
Although it is widely accepted that filaggrin (FLG) deficiency contributes to an abnormal barrier function in ichthyosis vulgaris… (More)
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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… (More)
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2009
Highly Cited
2009
Loss-of-function mutations in the FLG (filaggrin) gene cause the semidominant keratinizing disorder ichthyosis vulgaris and… (More)
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2008
2008
Mutations in the gene encoding filaggrin (FLG) have been identified as the cause of ichthyosis vulgaris (IV) and shown to be… (More)
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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… (More)
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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… (More)
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2006
Highly Cited
2006
Mutations in the filament aggregating protein (filaggrin) gene have recently been identified as the cause of the common genetic… (More)
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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… (More)
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2000
2000
Flaky tail (gene symbol ft) is an autosomal recessive mutation in mice that results in a dry, flaky skin, and annular tail and… (More)
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1985
1985
Ichthyosis vulgaris is an autosomal dominant disorder of keratinization characterized histologically by absent or reduced… (More)
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