Similar articles for PMID: 2887506

Year	Number of Results
1983	1
1985	2
1986	1
1987	3
1988	6
1989	13
1990	6
1991	7
1992	8
1993	9
1994	5
1995	8
1996	10
1997	6
1998	1
1999	3
2000	3
2001	3
2002	1
2003	1
2004	1
2007	2
2008	1
2016	2
2017	1
2020	1
2024	0

1

Familial hypercholesterolemia in South African Afrikaners. PvuII and StuI DNA polymorphisms in the LDL-receptor gene consistent with a predominating founder gene effect.

Brink PA, Steyn LT, Coetzee GA, Van der Westhuyzen DR. Brink PA, et al. Hum Genet. 1987 Sep;77(1):32-5. doi: 10.1007/BF00284709. Hum Genet. 1987. PMID: 2887506

2

Cascade Screening for Familial Hypercholesterolemia in South Africa: The Wits FIND-FH Program.

Raal FJ, Bahassi EM, Stevens B, Turner TA, Stein EA. Raal FJ, et al. Arterioscler Thromb Vasc Biol. 2020 Nov;40(11):2747-2755. doi: 10.1161/ATVBAHA.120.315040. Epub 2020 Sep 3. Arterioscler Thromb Vasc Biol. 2020. PMID: 32878475 Free article.

3

Molecular genetics of familial hypercholesterolemia in Israel-revisited.

Durst R, Ibe UK, Shpitzen S, Schurr D, Eliav O, Futema M, Whittall R, Szalat A, Meiner V, Knobler H, Gavish D, Henkin Y, Ellis A, Rubinstein A, Harats D, Bitzur R, Hershkovitz B, Humphries SE, Leitersdorf E. Durst R, et al. Atherosclerosis. 2017 Feb;257:55-63. doi: 10.1016/j.atherosclerosis.2016.12.021. Epub 2016 Dec 18. Atherosclerosis. 2017. PMID: 28104544 Free article.

4

Spectrum of mutations in homozygous familial hypercholesterolemia in India, with four novel mutations.

Setia N, Saxena R, Arora A, Verma IC. Setia N, et al. Atherosclerosis. 2016 Dec;255:31-36. doi: 10.1016/j.atherosclerosis.2016.10.028. Epub 2016 Oct 14. Atherosclerosis. 2016. PMID: 27816806

5

Evaluation of clinical diagnosis criteria of familial ligand defective apoB 100 and lipoprotein phenotype comparison between LDL receptor gene mutations affecting ligand-binding domain and the R3500Q mutation of the apoB gene in patients from a South European population.

Ejarque I, Real JT, Martinez-Hervas S, Chaves FJ, Blesa S, Garcia-Garcia AB, Millan E, Ascaso JF, Carmena R. Ejarque I, et al. Transl Res. 2008 Mar;151(3):162-7. doi: 10.1016/j.trsl.2007.12.001. Epub 2008 Jan 7. Transl Res. 2008. PMID: 18279815

6

[Familial hypercholesterolemia in St. Petersburg: diversity of mutations argues against a strong founder effect].

Zakharova FM, Tatishcheva IuA, Golubkov VI, Lipovetskiĭ BM, Konstantinov VO, Denisenko AD, Faergeman O, Vasil'ev VB, Mandel'shtam MIu. Zakharova FM, et al. Genetika. 2007 Sep;43(9):1255-62. Genetika. 2007. PMID: 17990524 Russian.

7

Two novel mutations of the LDL receptor gene associated with familial hypercholesterolemia in a Chinese family.

Xie L, Gong QH, Xie ZG, Liang ZM, Hu ZM, Xia K, Xia JH, Yang YF. Xie L, et al. Chin Med J (Engl). 2007 Oct 5;120(19):1694-9. Chin Med J (Engl). 2007. PMID: 17935672

8

[Identification of a novel splice mutation of low density lipoprotein receptor gene in a Chinese family with familial hypercholesterolemia].

Lin J, Wang LY, Liu S, Pan XD, Du LP, Shi FR, Qin YW, Zhao Q, Guo HY. Lin J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Feb;21(1):14-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 14767901 Chinese.

9

Allelic variation in the promoter region of the LDL receptor gene: analysis of an African-specific variant in the FP2 cis-acting regulatory element.

Hoogendijk CF, Scholtz CL, Pimstone SM, Ehrenborg E, Kastelein JJ, Defesche JC, Thiart R, du Plessis L, de Villiers JN, Zaahl MG, Delport R, Rubinsztein DC, Raffel LJ, Grim CE, Mediene-Benchekor S, Amouyel P, Brousseau T, Steyn K, Lombard CJ, Hayden MR, Kotze MJ. Hoogendijk CF, et al. Mol Cell Probes. 2003 Aug;17(4):175-81. doi: 10.1016/s0890-8508(03)00050-1. Mol Cell Probes. 2003. PMID: 12944120

10

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.

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