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dc.contributor.author Szamosi, Tamás
dc.contributor.author Szollar J
dc.contributor.author Meggyesi V
dc.contributor.author Wilhelm O
dc.contributor.author Bodánszky, Hedvig
dc.contributor.author Matyus J
dc.date.accessioned 2018-10-12T08:15:27Z
dc.date.available 2018-10-12T08:15:27Z
dc.date.issued 1984
dc.identifier 0021720726
dc.identifier.citation pagination=243-248; journalVolume=28; journalIssueNumber=2-3; journalTitle=MECHANISMS OF AGEING AND DEVELOPMENT;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/4841
dc.identifier.uri doi:10.1016/0047-6374(84)90024-1
dc.description.abstract Hutchinson-Gilford progeria was observed in two brothers. Their parents, sister and other relatives did not show any signs of this illness. Serum total cholesterol and total triglyceride levels were normal in the whole family. The serum high density lipoprotein cholesterol (HDL-C) level of parents was low and that of boys was extremely low. The serum HDL-C level of the healthy sister and other relatives was normal. These findings in homozygous children and heterozygous parents may explain the development of the very early fatal arteriosclerosis described in this disease. The connection between the disorder of the lipid metabolism and progeria can serve as a useful model in the study of the role of lipid metabolism in normal ageing.
dc.relation.ispartof urn:issn:0047-6374
dc.title Serum cholesterol and triglyceride levels in progeria as a model of ageing.
dc.type Journal Article
dc.date.updated 2018-02-19T12:08:28Z
dc.language.rfc3066 en
dc.identifier.mtmt 1614925
dc.identifier.wos A1984TY17500011
dc.identifier.pubmed 6521505
dc.contributor.department SE/AOK/K/II. Sz. Gyermekgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem


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