Linked Life Data

11837071

Source:http://linkedlifedata.com/resource/pubmed/id/11837071

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2002-2-11
pubmed:abstractText
Amyloidosis is a disorder of protein metabolism in which autologous proteins are deposited intercellularly as fibrils with characteristic staining properties and ultrastructural features. Amyloid deposits may be focal, localized to a particular tissue or organ, or distributed systemically. Many different chemical forms of amyloid have been identified and amyloid may accumulate as a result of a variety of different pathogenetic mechanisms. Amyloid deposits rarely regress, but rather tend to increase inexorably in size. Since there is no effective therapy for systemic forms of amyloidosis, they carry a poor prognosis in most cases.
pubmed:language
dut
pubmed:journal
pubmed:citationSubset
D
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0028-2200
pubmed:author
pubmed:issnType
Print
pubmed:volume
102
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
52-4
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed:year
1995
pubmed:articleTitle
[Amyloidosis. Etiology and clinical manifestations].
pubmed:affiliation
Afdeling Algemene Inwendige Geneeskunde, Academisch Ziekenhuis Vrije Universiteit, De Boelelaan 1117, 1081 HV Amsterdam.
pubmed:publicationType
Journal Article, English Abstract, Case Reports