Wang LY - Search Results

1

Seven-year clinical follow-up of a Chinese homozygous familial hypercholesterolemia child with premature xanthomas and coronary artery disease--a need for early diagnosis and aggressive treatment.

Jiang L, Gao F, Hu LB, Sun LY, Pan XD, Lin J, Zhang HB, Yong Q, Wang Q, Yang Y, Wang CM, Yang SW, Zhang F, Wang LY. Jiang L, et al. Among authors: wang ly, wang cm, wang q. Int J Cardiol. 2014 Nov 15;177(1):188-91. doi: 10.1016/j.ijcard.2014.09.058. Epub 2014 Sep 28. Int J Cardiol. 2014. PMID: 25499375 No abstract available.

2

Analysis of low-density lipoprotein receptor gene mutations in a Chinese patient with clinically homozygous familial hypercholesterolemia.

Cao S, Wang L, Qin Y, Lin J, Wu B, Liu S, Pan X, Du L, Chen B. Cao S, et al. Chin Med J (Engl). 2003 Oct;116(10):1535-8. Chin Med J (Engl). 2003. PMID: 14570618

3

[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. Among authors: wang ly. 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.

4

[The pathological changes of abdominal and peripheral arteries in familial hypercholesterolemia--the result of high-resolution color Doppler ultrasonography].

Yong Q, Sun H, Li ZA, Lin J, Wang LY. Yong Q, et al. Among authors: wang ly. Zhonghua Xin Xue Guan Bing Za Zhi. 2005 Apr;33(4):340-2. Zhonghua Xin Xue Guan Bing Za Zhi. 2005. PMID: 15932665 Chinese.

5

[Molecular basis of familial hypercholesterolemia-like phenotype heterogeneity].

Wang LY, Lin J, Liu S, Chen BS. Wang LY, et al. Yi Chuan Xue Bao. 2005 Jul;32(7):770-7. Yi Chuan Xue Bao. 2005. PMID: 16078748 Review. Chinese.

6

Functional analysis of low-density lipoprotein receptor in homozygous familial hypercholesterolemia patients with novel 1439 C-->T mutation of low-density lipoprotein receptor gene.

Lin J, Wang LY, Liu S, Xia JH, Yong Q, Du LP, Pan XD, Xue H, Chen BS, Jiang ZS. Lin J, et al. Among authors: wang ly. Chin Med J (Engl). 2008 May 5;121(9):776-81. Chin Med J (Engl). 2008. PMID: 18701038

7

A novel mutation in proprotein convertase subtilisin/kexin type 9 gene leads to familial hypercholesterolemia in a Chinese family.

Lin J, Wang LY, Liu S, Wang XM, Yong Q, Yang Y, DU LP, Pan XD, Wang X, Jiang ZS. Lin J, et al. Among authors: wang x, wang ly, wang xm. Chin Med J (Engl). 2010 May 5;123(9):1133-8. Chin Med J (Engl). 2010. PMID: 20529551

8

Evaluation of coronary flow velocity reserve in homozygous familial hypercholesterolemia by transthoracic Doppler echocardiography and dual-source computed tomography.

Yang Y, Zhang X, Li R, Ren H, Wang Z, Li Z, Lin J, Wang L, Yu W, Zhang Z. Yang Y, et al. Ultrasound Med Biol. 2010 Oct;36(10):1756-61. doi: 10.1016/j.ultrasmedbio.2010.05.013. Ultrasound Med Biol. 2010. PMID: 20800956

9

[Research progression of LDLR mutations in Chinese Familial hypercholesterolemia].

Dai YF, Sun LY, Zhang XB, Wang LY. Dai YF, et al. Among authors: wang ly. Yi Chuan. 2011 Jan;33(1):1-8. doi: 10.3724/sp.j.1005.2011.00001. Yi Chuan. 2011. PMID: 21377952 Review. Chinese.

10

Genome-wide linkage scan of a pedigree with familial hypercholesterolemia suggests susceptibility loci on chromosomes 3q25-26 and 21q22.

Wang X, Li X, Zhang YB, Zhang F, Sun L, Lin J, Wang DM, Wang LY. Wang X, et al. Among authors: wang ly, wang dm. PLoS One. 2011;6(10):e24838. doi: 10.1371/journal.pone.0024838. Epub 2011 Oct 14. PLoS One. 2011. PMID: 22022364 Free PMC article.

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