Similar articles for PMID: 18028451

Year	Number of Results
2000	1
2003	1
2004	8
2005	5
2006	7
2007	9
2008	7
2009	1
2010	3
2011	4
2012	6
2013	3
2014	3
2015	3
2017	2
2018	3
2024	0

1

Genetic heterogeneity of autosomal dominant hypercholesterolemia.

Varret M, Abifadel M, Rabès JP, Boileau C. Varret M, et al. Clin Genet. 2008 Jan;73(1):1-13. doi: 10.1111/j.1399-0004.2007.00915.x. Epub 2007 Nov 16. Clin Genet. 2008. PMID: 18028451 Review.

2

A Novel Cause of Familial Hypercholesterolemia: PCSK9 Gene Duplication.

Paquette M, Baass A. Paquette M, et al. Can J Cardiol. 2018 Oct;34(10):1259-1260. doi: 10.1016/j.cjca.2018.08.027. Epub 2018 Aug 18. Can J Cardiol. 2018. PMID: 30269825 No abstract available.

3

New prospects for PCSK9 inhibition?

Landmesser U, Chapman MJ, Stock JK, Amarenco P, Belch JJF, Borén J, Farnier M, Ference BA, Gielen S, Graham I, Grobbee DE, Hovingh GK, Lüscher TF, Piepoli MF, Ray KK, Stroes ES, Wiklund O, Windecker S, Zamorano JL, Pinto F, Tokgözoglu L, Bax JJ, Catapano AL; European Society of Cardiology/European Atherosclerosis Society Task Force. Landmesser U, et al. Eur Heart J. 2018 Jul 14;39(27):2600-2601. doi: 10.1093/eurheartj/ehy147. Eur Heart J. 2018. PMID: 29579192 Free article. No abstract available.

4

New Sequencing technologies help revealing unexpected mutations in Autosomal Dominant Hypercholesterolemia.

Elbitar S, Susan-Resiga D, Ghaleb Y, El Khoury P, Peloso G, Stitziel N, Rabès JP, Carreau V, Hamelin J, Ben-Djoudi-Ouadda A, Bruckert E, Boileau C, Seidah NG, Varret M, Abifadel M. Elbitar S, et al. Sci Rep. 2018 Jan 31;8(1):1943. doi: 10.1038/s41598-018-20281-9. Sci Rep. 2018. PMID: 29386597 Free PMC article.

5

Plasma lipoprotein(a) levels in patients with homozygous autosomal dominant hypercholesterolemia.

Sjouke B, Yahya R, Tanck MWT, Defesche JC, de Graaf J, Wiegman A, Kastelein JJP, Mulder MT, Hovingh GK, Roeters van Lennep JE. Sjouke B, et al. J Clin Lipidol. 2017 Mar-Apr;11(2):507-514. doi: 10.1016/j.jacl.2017.02.010. Epub 2017 Feb 27. J Clin Lipidol. 2017. PMID: 28502508

6

Impact of rare variants in autosomal dominant hypercholesterolemia causing genes.

Calandra S, Tarugi P, Bertolini S. Calandra S, et al. Curr Opin Lipidol. 2017 Jun;28(3):267-272. doi: 10.1097/MOL.0000000000000414. Curr Opin Lipidol. 2017. PMID: 28323660 Review.

7

Characterization of the first PCSK9 gain of function homozygote.

Alves AC, Etxebarria A, Medeiros AM, Benito-Vicente A, Thedrez A, Passard M, Croyal M, Martin C, Lambert G, Bourbon M. Alves AC, et al. J Am Coll Cardiol. 2015 Nov 10;66(19):2152-2154. doi: 10.1016/j.jacc.2015.08.871. J Am Coll Cardiol. 2015. PMID: 26541928 Free article. No abstract available.

8

A conversation with Helen Hobbs.

Hobbs H, Neill US. Hobbs H, et al. J Clin Invest. 2015 Oct 1;125(10):3725-6. doi: 10.1172/JCI84086. Epub 2015 Oct 1. J Clin Invest. 2015. PMID: 26426073 Free PMC article. No abstract available.

9

[Familial hypercholesterolemia due to a new mutation in the low density lipoprotein receptor gene].

Korneva VA, Bogoslovskaia TIu, Kuznetsova TIu, Mandel'shtam MIu, Vasil'ev VB. Korneva VA, et al. Klin Med (Mosk). 2014;92(7):49-53. Klin Med (Mosk). 2014. PMID: 25775905 Russian.

10

Genetics of familial hypercholesterolemia.

Brautbar A, Leary E, Rasmussen K, Wilson DP, Steiner RD, Virani S. Brautbar A, et al. Curr Atheroscler Rep. 2015 Apr;17(4):491. doi: 10.1007/s11883-015-0491-z. Curr Atheroscler Rep. 2015. PMID: 25712136 Review.

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