About: The peeling skin syndrome

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

scientific article published on 01 November 1982

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в листопаді 1982 (uk) im November 1982 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 01 November 1982 (en) artículu científicu espublizáu en payares de 1982 (ast)
publication date	wds:Q70515957-89FAC3F2-17E3-4DF7-B6F4-931F52F5AAFB
publication date	1982-11-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q70515957-A0DD1405-1C8E-4EF9-92DD-8393AAA7C977
language of work or name	English
cites work	wds:Q70515957-08A4D360-4739-46F5-B24E-535381AED6FB wds:Q70515957-22A3270E-1CFB-4553-AEA5-C15C2C441914 wds:Q70515957-2B84A74C-40C5-4E5F-AA72-552B86E64FA5 wds:Q70515957-79CB70D6-2076-43B2-834C-8A75B55A8335 wds:Q70515957-8CEA8004-5D48-4F84-8C7F-EFC06BFC91C9 wds:Q70515957-9C7FDA14-CB20-49E8-901F-656DC0A2476D wds:Q70515957-D98AA86A-FE80-4426-A57D-297D36B3229E wds:Q70515957-EF434553-B2D1-4033-92A0-4960F040D7C4
cites work	Refsum's disease--a recently characterized lipidosis involving the nervous system. Combined clinical staff conference at the National Institutes of Health Enzymatic basis of typical X-linked icthyosis The cornified envelope of terminally differentiated human epidermal keratinocytes consists of cross-linked protein Ichthyosiform dermatoses. Classification based on anatomic and biometric observations Human Epidermal Transamidase Lamellar ichthyosis, dwarfism, mental retardation, and hair shaft abnormalities. A link between the ichthyosis-associated and BIDS syndromes. Examination of the epidermis by the strip method of removing horny layers. I. Observations on thickness of the horny layer, and on mitotic activity after stripping Familial Hypogonadotropic Hypogonadism With Anosmia
author name string	wds:Q70515957-75FB7369-A04C-4F3F-95B7-F04C19320594 wds:Q70515957-F32BBFAC-F401-4C3B-A476-7E235DF397AC
author name string	S B Levy L A Goldsmith
rdfs:label	The peeling skin syndrome (en) The peeling skin syndrome (nl)
skos:prefLabel	The peeling skin syndrome (en) The peeling skin syndrome (nl)
name	The peeling skin syndrome (en) The peeling skin syndrome (nl)
title	wds:Q70515957-D5EDAB94-334F-4E8D-A17C-D6BD61D05FEF
title	The peeling skin syndrome (en)
page(s)	wds:Q70515957-48A43172-7D45-404F-906A-A1088220D2D3
page(s)	606-613
instance of	wds:Q70515957-4E38AE83-2B1C-4ECD-BE2B-F4B33E9E4F41
instance of	scholarly article
main subject	wds:Q70515957-1CC0C4AA-64A7-4DC3-8DC2-51720654E0EB
main subject	peeling skin syndrome
PubMed ID	wds:Q70515957-298D96D6-E381-4051-956D-21B5D137C7D8
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7142468
PubMed ID	7142468
published in	wds:Q70515957-02011B3A-F229-4634-B53C-AA7FE1FD861A
published in	Journal of the American Academy of Dermatology
issue	wds:Q70515957-4F4532DE-2AE7-4520-B445-9964AE312C82
volume	wds:Q70515957-E4F9EA3D-1D06-4212-8B83-D7E4BF3EA067
issue	5
volume	7
DOI	wds:Q70515957-8989C4D3-5853-4D9A-845E-86E4E2534FF3
DOI	http://dx.doi.org/10.1016/S0190-9622(82)70140-9
DOI	10.1016/S0190-9622(82)70140-9
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q70515957
is cites work of	Adult-onset acral peeling skin syndrome in a non-identical twin: a case report in South Africa Peeling skin syndrome: genetic defects in late terminal differentiation of the epidermis. Ichthyosiform dermatosis with superficial blister formation and peeling: evidence for a desmosomal anomaly and altered epidermal vitamin A metabolism A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease A Case of Peeling Skin Syndrome A Case of Inflammatory Generalized Type of Peeling Skin Syndrome Possibly Caused by a Homozygous Missense Mutation of CDSN. Peeling skin syndrome: 11 cases from Saudi Arabia. Peeling skin syndrome Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type A Peeling skin syndrome Loose anagen syndrome and loose anagen hair
is cites work of	wds:Q35056783-43C75E6F-B41E-4D07-BF0D-E9C1AC9BCA10 wds:Q41878111-9F854BB7-F37F-4ED4-8B59-2D82D44D369B wds:Q53438975-92A0FD35-2E55-467A-A6D2-1025EEA4AB1C wds:Q42607143-04744D6E-41A0-440E-83FB-D423F226BCE9 wds:Q53595495-CC28E3C5-AC83-42EF-A904-F31B847B608A wds:Q69843244-4E49DD94-A9D7-4CA3-98AB-1B70E8184B17 wds:Q24294533-019369B3-220D-4066-A276-429ED23BCBE8 wds:Q24538571-27B1050D-1CF6-4A1D-864C-4F2F09434691 wds:Q40798960-D0E5CBDE-8B5F-43DE-ACD8-E39EA6F77014 wds:Q41545477-24145835-A712-4F13-AB47-31622B0AE7DC wds:Q60549442-3E683F31-9483-42A2-AB02-2A2DCE723880 wds:Q71131592-88444283-7BE7-4C2B-B77A-17808903C55E

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