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Nonsyndromic types of ichthyoses - an update
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title
Nonsyndromic types of ichthyoses - an update
(English)
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PubMed
author name string
Heiko Traupe
series ordinal
1
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Crossref
Judith Fischer
series ordinal
2
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Crossref
Vinzenz Oji
series ordinal
3
1 reference
stated in
Crossref
language of work or name
English
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stated in
PubMed
publication date
February 2014
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PubMed
published in
JDDG
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PubMed
volume
12
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stated in
PubMed
issue
2
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stated in
PubMed
page(s)
109-21
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PubMed
cites work
Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FDDG.12229
retrieved
21 January 2018
Development of ichthyosiform skin compensates for defective permeability barrier function in mice lacking transglutaminase 1
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1111%2FDDG.12229
retrieved
21 January 2018
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.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FDDG.12229
retrieved
21 January 2018
Complete filaggrin deficiency in ichthyosis vulgaris is associated with only moderate changes in epidermal permeability barrier function profile
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1111%2FDDG.12229
retrieved
21 January 2018
X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits
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stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FDDG.12229
retrieved
21 January 2018
Prevalence of autosomal recessive congenital ichthyosis: a population-based study using the capture-recapture method in Spain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FDDG.12229
retrieved
21 January 2018
Genotypic and clinical spectrum of self-improving collodion ichthyosis: ALOX12B, ALOXE3, and TGM1 mutations in Scandinavian patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FDDG.12229
retrieved
21 January 2018
Ichthyosis vulgaris: novelFLGmutations in the German population and high presence of CD1a+ cells in the epidermis of the atopic subgroup
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FDDG.12229
retrieved
21 January 2018
Autosomal recessive congenital ichthyosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FDDG.12229
retrieved
7 January 2021
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Identifiers
DOI
10.1111/DDG.12229
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PubMed publication ID
24119255
1 reference
stated in
PubMed
ResearchGate publication ID
257752270
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