Zobrazeno 1 - 10
of 14
pro vyhledávání: '"D M Kusters"'
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 164
A recent Dutch study in patients with familial hypercholesterolaemia (FH), suggests that long-term statin treatment initiated at childhood reduces the risk for cardiovascular events in adulthood. None of the patients developed rhabdomyolysis or other
Autor:
Paul D. Martin, Albert Wiegman, urner T, Joel S. Raichlen, Claude Gagné, Marjet J.A.M. Braamskamp, Barbara A. Hutten, Gisle Langslet, Elinor Miller, David Cassiman, Evan A. Stein, Katherine M. Morrison, Brian W. McCrindle, Daniel Gaudet, D. M. Kusters, Gordon A. Francis, Kastelein Jjp
Publikováno v:
Circulation, 136(4), 359-366. Lippincott Williams and Wilkins
Background: Heterozygous familial hypercholesterolemia (HeFH) is an autosomal dominant disorder leading to premature atherosclerosis. Children with HeFH exhibit early signs of atherosclerosis manifested by increased carotid intima-media thickness (IM
Autor:
Joost Besseling, G. Kees Hovingh, Barbara Sjouke, Anton F. H. Stalenhoef, Albert Wiegman, Sigrid W. Fouchier, Joep C. Defesche, John J.P. Kastelein, Jeanine E. Roeters van Lennep, D. M. Kusters, Jacqueline de Graaf, Eric J.G. Sijbrands, Iris Kindt
Publikováno v:
European Heart Journal, 36, 560-5
European Heart Journal, 36, 9, pp. 560-5
European Heart Journal, 36(9), 560-565. Oxford University Press
European heart journal, 36(9), 560-565. Oxford University Press
European Heart Journal, 36, 9, pp. 560-5
European Heart Journal, 36(9), 560-565. Oxford University Press
European heart journal, 36(9), 560-565. Oxford University Press
Item does not contain fulltext AIMS: Homozygous autosomal dominant hypercholesterolaemia (hoADH), an orphan disease caused by mutations in low-density lipoprotein receptor (LDLR), apolipoprotein B (APOB), or proprotein convertase subtilisin-kexin typ
Publikováno v:
Archives of Disease in Childhood. 97:272-276
Different screening strategies are currently recommended to identify children with (familial) hypercholesterolaemia in order to initiate early lipid management. However, these strategies are characterised to date by low adherence by the medical commu
Publikováno v:
Atherosclerosis Supplements. 32:32
Autor:
D. M. Kusters, R. Huijgen, J. C. Defesche, M. N. Vissers, I. Kindt, B. A. Hutten, J. J. P. Kastelein
Publikováno v:
De Nederlandse gezondheidszorg ISBN: 9789036807043
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edb8825a9f991ad7abe1cb7e476e616c
https://doi.org/10.1007/978-90-368-0705-0_13
https://doi.org/10.1007/978-90-368-0705-0_13
Publikováno v:
Circulation research, 114(2), 307-310. Lippincott Williams and Wilkins
Rationale: Familial hypercholesterolemia (FH) predisposes patients to premature cardiovascular disease, with the process of atherosclerosis initiated in early childhood. Objective: As part of an ongoing trial to assess the efficacy and safety of rosu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::133f852897b6852f782d889d2bee88f0
https://pure.amc.nl/en/publications/carotid-intimamedia-thickness-in-children-with-familial-hypercholesterolemia(269c9177-c491-4678-895c-79837421130b).html
https://pure.amc.nl/en/publications/carotid-intimamedia-thickness-in-children-with-familial-hypercholesterolemia(269c9177-c491-4678-895c-79837421130b).html
Publikováno v:
Archives of Disease in Childhood, 97(3), 272-276. (2012).
Archives of Disease in Childhood, 97(3), 272-276. London, United Kingdom: British Medical Association (2011).
Archives of Disease in Childhood, 97(3), 272-276. London, United Kingdom: British Medical Association (2011).
Different screening strategies are currently recommended to identify children with (familial) hypercholesterolaemia in order to initiate early lipid management. However, these strategies are characterised to date by low adherence by the medical commu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8152e63f495fdaa7bde606de0fe52d71
http://orbilu.uni.lu/handle/10993/27176
http://orbilu.uni.lu/handle/10993/27176
Autor:
M. N. Vissers, Joep C. Defesche, Barbara A. Hutten, Iris Kindt, R. Huijgen, John J. P. Kastelein, D. M. Kusters
Publikováno v:
Netherlands Heart Journal
Netherlands heart journal, 19(4), 175-182. Bohn Stafleu van Loghum
Netherlands heart journal, 19(4), 175-182. Bohn Stafleu van Loghum
BACKGROUND: In the Netherlands, a screening programme was set up in 1994 in order to identify all patients with familial hypercholesterolaemia (FH). After 15 years of screening, we evaluated the geographical distribution, possible founder effects and
Autor:
D M, Kusters, S J M, Homsma, B A, Hutten, M T B, Twickler, H J, Avis, J A, van der Post, E S G, Stroes
Publikováno v:
The Netherlands journal of medicine. 68(1)
Familial hypercholesterolaemia (FH) is a co-dominant monogenic disorder of lipoprotein metabolism, characterised by severely elevated levels of low-density lipoprotein cholesterol (LDL-C) from birth onwards. Treatment of FH patients with cholesterol-