Similar articles for PMID: 15823288

Year	Number of Results
1987	1
1989	1
1995	1
1996	1
1998	4
2001	1
2002	2
2003	1
2004	5
2005	6
2006	4
2008	4
2010	2
2011	2
2012	3
2013	2
2014	2
2015	3
2016	6
2017	7
2018	2
2019	2
2020	3
2022	1
2024	0

1

The relationship of molecular genetic to clinical diagnosis of familial hypercholesterolemia in a Danish population.

Damgaard D, Larsen ML, Nissen PH, Jensen JM, Jensen HK, Soerensen VR, Jensen LG, Faergeman O. Damgaard D, et al. Atherosclerosis. 2005 May;180(1):155-60. doi: 10.1016/j.atherosclerosis.2004.12.001. Epub 2005 Jan 12. Atherosclerosis. 2005. PMID: 15823288

2

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

Jensen HK. Jensen HK. Dan Med Bull. 2002 Nov;49(4):318-45. Dan Med Bull. 2002. PMID: 12553167 Review.

3

Clinical features of familial hypercholesterolemia in Korea: Predictors of pathogenic mutations and coronary artery disease - A study supported by the Korean Society of Lipidology and Atherosclerosis.

Shin DG, Han SM, Kim DI, Rhee MY, Lee BK, Ahn YK, Cho BR, Woo JT, Hur SH, Jeong JO, Jang Y, Lee JH, Lee SH. Shin DG, et al. Atherosclerosis. 2015 Nov;243(1):53-8. doi: 10.1016/j.atherosclerosis.2015.08.033. Epub 2015 Sep 5. Atherosclerosis. 2015. PMID: 26343872

4

Comparison of genetic versus clinical diagnosis in familial hypercholesterolemia.

Civeira F, Ros E, Jarauta E, Plana N, Zambon D, Puzo J, Martinez de Esteban JP, Ferrando J, Zabala S, Almagro F, Gimeno JA, Masana L, Pocovi M. Civeira F, et al. Am J Cardiol. 2008 Nov 1;102(9):1187-93, 1193.e1. doi: 10.1016/j.amjcard.2008.06.056. Epub 2008 Aug 27. Am J Cardiol. 2008. PMID: 18940289

5

A Comparative Analysis of Phenotypic Predictors of Mutations in Familial Hypercholesterolemia.

Chan DC, Pang J, Hooper AJ, Bell DA, Bates TR, Burnett JR, Watts GF. Chan DC, et al. J Clin Endocrinol Metab. 2018 Apr 1;103(4):1704-1714. doi: 10.1210/jc.2017-02622. J Clin Endocrinol Metab. 2018. PMID: 29408959

6

Genetic mutations in patients with possible familial hypercholesterolaemia in South East Scotland.

Ho CK, Stirling D, Hannant W, Walker SW. Ho CK, et al. Scott Med J. 2012 Aug;57(3):148-51. doi: 10.1258/smj.2012.012020. Scott Med J. 2012. PMID: 22859806

7

An APEX-based genotyping microarray for the screening of 168 mutations associated with familial hypercholesterolemia.

Dušková L, Kopečková L, Jansová E, Tichý L, Freiberger T, Zapletalová P, Soška V, Ravčuková B, Fajkusová L. Dušková L, et al. Atherosclerosis. 2011 May;216(1):139-45. doi: 10.1016/j.atherosclerosis.2011.01.023. Epub 2011 Jan 21. Atherosclerosis. 2011. PMID: 21310417

8

The molecular basis of familial hypercholesterolemia in the Czech Republic: spectrum of LDLR mutations and genotype-phenotype correlations.

Tichý L, Freiberger T, Zapletalová P, Soška V, Ravčuková B, Fajkusová L. Tichý L, et al. Atherosclerosis. 2012 Aug;223(2):401-8. doi: 10.1016/j.atherosclerosis.2012.05.014. Epub 2012 May 23. Atherosclerosis. 2012. PMID: 22698793

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. Huijgen R, et al. Hum Mutat. 2010 Jun;31(6):752-60. doi: 10.1002/humu.21258. Hum Mutat. 2010. PMID: 20506408

10

Update of the molecular basis of familial hypercholesterolemia in The Netherlands.

Fouchier SW, Kastelein JJ, Defesche JC. Fouchier SW, et al. Hum Mutat. 2005 Dec;26(6):550-6. doi: 10.1002/humu.20256. Hum Mutat. 2005. PMID: 16250003

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

62 results

Results by year