Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 170

1.

Assessment of carotid atherosclerosis in normocholesterolemic individuals with proven mutations in the low-density lipoprotein receptor or apolipoprotein B genes.

Huijgen R, Vissers MN, Kindt I, Trip MD, de Groot E, Kastelein JJ, Hutten BA.

Circ Cardiovasc Genet. 2011 Aug 1;4(4):413-7. doi: 10.1161/CIRCGENETICS.110.959239. Epub 2011 Jun 4.

2.

The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.

Jensen HK.

Dan Med Bull. 2002 Nov;49(4):318-45. Review.

PMID:
12553167
3.

Discriminative ability of LDL-cholesterol to identify patients with familial hypercholesterolemia: a cross-sectional study in 26,406 individuals tested for genetic FH.

Huijgen R, Hutten BA, Kindt I, Vissers MN, Kastelein JJ.

Circ Cardiovasc Genet. 2012 Jun;5(3):354-9. doi: 10.1161/CIRCGENETICS.111.962456. Epub 2012 May 2.

4.

Low-density lipoprotein receptor gene mutations and cardiovascular risk in a large genetic cascade screening population.

Umans-Eckenhausen MA, Sijbrands EJ, Kastelein JJ, Defesche JC.

Circulation. 2002 Dec 10;106(24):3031-6.

5.
6.

Influence of HDL cholesterol on preclinical carotid atherosclerosis in familial hypercholesterolemia.

Junyent M, Cofán M, Núñez I, Gilabert R, Zambón D, Ros E.

Arterioscler Thromb Vasc Biol. 2006 May;26(5):1107-13. Epub 2006 Mar 23.

7.

Lp(a) levels and atherosclerotic vascular disease in a sample of patients with familial hypercholesterolemia sharing the same gene defect.

Carmena R, Lussier-Cacan S, Roy M, Minnich A, Lingenhel A, Kronenberg F, Davignon J.

Arterioscler Thromb Vasc Biol. 1996 Jan;16(1):129-36.

8.

Low-density lipoprotein receptor genotype and response to pravastatin in children with familial hypercholesterolemia: substudy of an intima-media thickness trial.

Koeijvoets KC, Rodenburg J, Hutten BA, Wiegman A, Kastelein JJ, Sijbrands EJ.

Circulation. 2005 Nov 15;112(20):3168-73.

9.

Functionality of sequence variants in the genes coding for the low-density lipoprotein receptor and apolipoprotein B in individuals with inherited hypercholesterolemia.

Huijgen R, Kindt I, Fouchier SW, Defesche JC, Hutten BA, Kastelein JJ, Vissers MN.

Hum Mutat. 2010 Jun;31(6):752-60. doi: 10.1002/humu.21258.

PMID:
20506408
10.

Impact of genetic defects on atherosclerosis in patients suspected of familial hypercholesterolaemia.

Descamps OS, Gilbeau JP, Leysen X, Van Leuven F, Heller FR.

Eur J Clin Invest. 2001 Nov;31(11):958-65.

PMID:
11737238
11.

Low-density lipoprotein levels and not mutation status predict intima-media thickness in familial hypercholesterolemia.

Fahed AC, Habib RH, Nemer GM, Azar ST, Andary RR, Arabi MT, Moubarak EM, Bitar FF, Haddad FF.

Ann Vasc Surg. 2014 Feb;28(2):421-6. doi: 10.1016/j.avsg.2013.02.024. Epub 2013 Oct 9.

PMID:
24120234
12.

Carotid atherosclerosis and lipoprotein particle subclasses in familial hypercholesterolaemia and familial combined hyperlipidaemia.

Jarauta E, Mateo-Gallego R, Gilabert R, Plana N, Junyent M, de Groot E, Cenarro A, Masana L, Ros E, Civeira F.

Nutr Metab Cardiovasc Dis. 2012 Jul;22(7):591-7. doi: 10.1016/j.numecd.2010.10.011. Epub 2010 Dec 31.

PMID:
21196102
13.

One-year atorvastatin treatment in hypercholesterolemic patients with or without carotid artery disease.

Avellone G, Di Garbo V, Abruzzese G, Campisi D, De Simone R, Raneli G, Licata G.

Int Angiol. 2006 Mar;25(1):26-34.

14.

Familial hypercholesterolemia: molecular, biochemical, and clinical characterization of a French-Canadian pediatric population.

Assouline L, Levy E, Feoli-Fonseca JC, Godbout C, Lambert M.

Pediatrics. 1995 Aug;96(2 Pt 1):239-46.

PMID:
7630677
15.

Differences in the phenotype between children with familial defective apolipoprotein B-100 and familial hypercholesterolemia.

Pimstone SN, Defesche JC, Clee SM, Bakker HD, Hayden MR, Kastelein JJ.

Arterioscler Thromb Vasc Biol. 1997 May;17(5):826-33.

16.
17.

Influence of LDL receptor gene mutations and the R3500Q mutation of the apoB gene on lipoprotein phenotype of familial hypercholesterolemic patients from a South European population.

Real JT, Chaves FJ, Ejarque I, García-García AB, Valldecabres C, Ascaso JF, Armengod ME, Carmena R.

Eur J Hum Genet. 2003 Dec;11(12):959-65.

18.

Familial defective apolipoprotein B versus familial hypercholesterolemia: an assessment of risk.

Fouchier SW, Defesche JC, Kastelein JJ, Sijbrands EJ.

Semin Vasc Med. 2004 Aug;4(3):259-64.

PMID:
15630635
19.

LDL receptor mutation genotype and vascular disease phenotype in heterozygous familial hypercholesterolaemia.

Brorholt-Petersen JU, Jensen HK, Jensen JM, Refsgaard J, Christiansen T, Hansen LB, Gregersen N, Faergeman O.

Clin Genet. 2002 Jun;61(6):408-15.

PMID:
12121347
20.

[Lipoprotein(a) is associated to atherosclerosis in primary hypercholesterolemia].

Bea AM, Mateo-Gallego R, Jarauta E, Villa-Pobo R, Calmarza P, Lamiquiz-Moneo I, Cenarro A, Civeira F.

Clin Investig Arterioscler. 2014 Jul-Aug;26(4):176-83. doi: 10.1016/j.arteri.2014.01.001. Epub 2014 Feb 25. Spanish.

PMID:
24576773

Supplemental Content

Support Center