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10534628
Source:
http://linkedlifedata.com/resource/pubmed/id/10534628
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0007320
,
umls-concept:C0022378
,
umls-concept:C0023866
,
umls-concept:C0030705
,
umls-concept:C0085973
,
umls-concept:C0153619
,
umls-concept:C0205420
,
umls-concept:C0282443
,
umls-concept:C1321489
,
umls-concept:C1552617
pubmed:issue
5 Pt 1
pubmed:dateCreated
1999-12-7
pubmed:abstractText
Muir-Torre syndrome is a rare autosomal dominant genodermatosis, first described in 1967, characterized by the presence of sebaceous tumors and an internal malignancy in the absence of other predisposing factors.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/10534628-10534651
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/7907132
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0190-9622
pubmed:author
pubmed-author:AkhtarSS
,
pubmed-author:KhanS ASA
,
pubmed-author:LamD TDT
,
pubmed-author:WrightJJ
pubmed:issnType
Print
pubmed:volume
41
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
681-6
pubmed:dateRevised
2005-11-16
pubmed:meshHeading
pubmed-meshheading:10534628-Adenoma
,
pubmed-meshheading:10534628-Aged
,
pubmed-meshheading:10534628-Humans
,
pubmed-meshheading:10534628-Keratoacanthoma
,
pubmed-meshheading:10534628-Male
,
pubmed-meshheading:10534628-Neoplasms, Multiple Primary
,
pubmed-meshheading:10534628-Skin Diseases
,
pubmed-meshheading:10534628-Skin Neoplasms
,
pubmed-meshheading:10534628-Syndrome
,
pubmed-meshheading:10534628-Ureteral Neoplasms
pubmed:year
1999
pubmed:articleTitle
Muir-Torre syndrome: case report of a patient with concurrent jejunal and ureteral cancer and a review of the literature.
pubmed:affiliation
Department of Medicine, University Hospital, State University of New York, Health Science Center at Syracuse, New York, USA. akhtars@pol.net
pubmed:publicationType
Journal Article
,
Review
,
Case Reports