Source:http://linkedlifedata.com/resource/pubmed/id/15168045
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2004-10-13
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pubmed:abstractText |
Hereditary hemorrhagic telangiectasia (HHT) (the Osler-Weber-Rendu syndrome) is a rare autosomal dominant disease characterized by telangiectasias and arteriovenous malformations of the upper and lower respiratory tract, gastrointestinal tract, skin and central nervous system. Several previous reports have documented the appearance of a concomitant neoplasm in patients with this syndrome.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0179-1958
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
595-8
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pubmed:meshHeading |
pubmed-meshheading:15168045-Adenocarcinoma,
pubmed-meshheading:15168045-Cohort Studies,
pubmed-meshheading:15168045-Colonic Neoplasms,
pubmed-meshheading:15168045-Colonic Polyps,
pubmed-meshheading:15168045-Colonoscopy,
pubmed-meshheading:15168045-Female,
pubmed-meshheading:15168045-Gastrointestinal Hemorrhage,
pubmed-meshheading:15168045-Humans,
pubmed-meshheading:15168045-Male,
pubmed-meshheading:15168045-Retrospective Studies,
pubmed-meshheading:15168045-Telangiectasia, Hereditary Hemorrhagic
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pubmed:year |
2004
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pubmed:articleTitle |
Does any lower gastrointestinal bleeding in patients suffering from hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu) necessitate a full colonic visualization?
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pubmed:affiliation |
Department of Medicine, Mount Scopus Hadassah Hospital, P.O. Box 24035, Jerusalem 91240, Israel.
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pubmed:publicationType |
Journal Article
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