Du R - Search Results

1

Novel variants and phenotypic heterogeneity in a cohort of 11 Chinese children with Wiedemann-Steiner syndrome.

Lin Y, Chen X, Xie B, Guan Z, Chen X, Li X, Yi P, Du R, Mei H, Liu L, Zhang W, Zeng C. Lin Y, et al. Among authors: du r. Front Genet. 2023 Mar 21;14:1085210. doi: 10.3389/fgene.2023.1085210. eCollection 2023. Front Genet. 2023. PMID: 37025457 Free PMC article.

2

Mutation analysis of KCNQ1, KCNH2, SCN5A, KCNE1 and KCNE2 genes in Chinese patients with long QT syndrome.

Du R, Tian L, Yuan G, Li J, Ren F, Gui L, Li W, Zhang S, Kang C, Yang J. Du R, et al. Front Med China. 2007 Jul;1(3):312-5. doi: 10.1007/s11684-007-0060-0. Epub 2007 Jul 1. Front Med China. 2007. PMID: 24573873

3

[Mutation analysis of a Chinese family with inherited long QT syndrome].

Du R, Yang JG, Li W, Gui L, Yuan GH, Kang CL, Ren FX, Zhang SY. Du R, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Feb;22(1):68-70. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15696484 Chinese.

4

Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.

Liu F, Li P, Liu Y, Li W, Wong F, Du R, Wang L, Li C, Jiang F, Tang Z, Liu M. Liu F, et al. Among authors: du r. Mol Vis. 2013;19:695-701. Epub 2013 Mar 21. Mol Vis. 2013. PMID: 23559863 Free PMC article.

5

[Study on novel mutations of MEF2A gene in Chinese patients with coronary artery disease].

Li J, Yang JG, Li W, Du R, Gui L, Tian L, Guo QH. Li J, et al. Among authors: du r. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Jun;23(3):265-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16767660 Chinese.

6

MEF2A gene mutations and susceptibility to coronary artery disease in the Chinese population.

Li J, Chen HX, Yang JG, Li W, Du R, Tian L. Li J, et al. Among authors: du r. Genet Mol Res. 2014 Oct 20;13(4):8396-402. doi: 10.4238/2014.October.20.15. Genet Mol Res. 2014. PMID: 25366733 Free article.

7

[Systemic lupus erythematosus associated macrophage activation syndrome with neuropsychiatric symptoms: A report of 2 cases].

Luo ZJ, Wu JJ, Song Y, Mei CL, DU R. Luo ZJ, et al. Among authors: du r. Beijing Da Xue Xue Bao Yi Xue Ban. 2023 Dec 18;55(6):1111-1117. doi: 10.19723/j.issn.1671-167X.2023.06.024. Beijing Da Xue Xue Bao Yi Xue Ban. 2023. PMID: 38101797 Free PMC article. Chinese.

8

A novel SCN1A missense mutation causes generalized epilepsy with febrile seizures plus in a Chinese family.

Cui X, Zeng F, Liu Y, Zhang J, Archacki S, Zhan T, Du R, Tang Z, Liu J, Wang QK, Liu M. Cui X, et al. Among authors: du r. Neurosci Lett. 2011 Sep 26;503(1):27-30. doi: 10.1016/j.neulet.2011.08.001. Epub 2011 Aug 6. Neurosci Lett. 2011. PMID: 21843600

9

[Relationship between congenital long QT syndrome and Brugada syndrome gene mutation].

Du R, Ren FX, Yang JG, Yuan GH, Zhang SY, Kang CL, Li W, Gui L, Li J. Du R, et al. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2005 Jun;27(3):289-94. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2005. PMID: 16038262 Chinese.

10

[Gene mutation in secundum atrial septal defect: analysis of a Chinese family with 3 patients].

Tian L, Zhu JF, Yang JG, Zhu QH, Du R, Li J, Li W. Tian L, et al. Among authors: du r. Zhonghua Yi Xue Za Zhi. 2008 Jan 22;88(4):250-3. Zhonghua Yi Xue Za Zhi. 2008. PMID: 18361836 Chinese.

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