Nonsyndromic types of ichthyoses - an update - Wikidata - awgldk - TriplyDB

Nonsyndromic types of ichthyoses - an update

Nonsyndromic types of ichthyoses - an update

http://www.wikidata.org/entity/Q26824927

about

Ichthyosis with confetti: clinics, molecular genetics and management Diagnosis of Atopic Dermatitis: Mimics, Overlaps, and Complications Genetics and genomics in Brazil: a promising future The effect of two endogenous retinoids on the mRNA expression profile in human primary keratinocytes, focusing on genes causing autosomal recessive congenital ichthyosis Essential role of the cytochrome P450 CYP4F22 in the production of acylceramide, the key lipid for skin permeability barrier formation.Autosomal Recessive Congenital Ichthyosis in American Bulldogs Is Associated With NIPAL4 (ICHTHYIN) Deficiency.The Effect of Dietary Change in a Patient With Ichthyosis Vulgaris: A Case Report Role of molecular testing in the multidisciplinary diagnostic approach of ichthyosis.PNPLA1 Deficiency in Mice and Humans Leads to a Defect in the Synthesis of Omega-O-Acylceramides.Neurological Manifestations of X-Linked Ichthyosis: Case Report and Review of the Literature.High levels of oxysterol sulfates in serum of patients with steroid sulfatase deficiency.PNPLA1 is a transacylase essential for the generation of the skin barrier lipid ω-O-acylceramide.Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans.Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.Alitretinoin reduces erythema in inherited ichthyosis.

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P2860

Nonsyndromic types of ichthyoses - an update

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2014 nî lūn-bûn

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2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2014 թվականի փետրվարին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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Nonsyndromic types of ichthyoses - an update

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Nonsyndromic types of ichthyoses - an update

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Nonsyndromic types of ichthyoses - an update

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Heiko Traupe

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Judith Fischer

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Vinzenz Oji

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P2860

Filaggrin haploinsufficiency is highly penetrant and is associated with increased severity of eczema: further delineation of the skin phenotype in a prospective epidemiological study of 792 school children.

Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009.

Development of ichthyosiform skin compensates for defective permeability barrier function in mice lacking transglutaminase 1

Genotypic and clinical spectrum of self-improving collodion ichthyosis: ALOX12B, ALOXE3, and TGM1 mutations in Scandinavian patients.

Complete filaggrin deficiency in ichthyosis vulgaris is associated with only moderate changes in epidermal permeability barrier function profile.

Prevalence of autosomal recessive congenital ichthyosis: a population-based study using the capture-recapture method in Spain.

X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits.

Ichthyosis vulgaris: novelFLGmutations in the German population and high presence of CD1a+ cells in the epidermis of the atopic subgroup

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