Nie LL - Search Results

1

[Mutation analysis of ATP13A2 gene in Chinese patients with familial autosomal recessive early-onset parkinsonism].

He D, Guo JF, Wang L, Xiao ZQ, Nie LL, Zhang XW, Tang BS. He D, et al. Among authors: nie ll. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Oct;26(5):567-70. doi: 10.3760/cma.j.issn.1003-9406.2009.05.020. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19806583 Chinese.

2

Mutation analysis of Parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset Parkinsonism.

Guo JF, Xiao B, Liao B, Zhang XW, Nie LL, Zhang YH, Shen L, Jiang H, Xia K, Pan Q, Yan XX, Tang BS. Guo JF, et al. Among authors: nie ll. Mov Disord. 2008 Oct 30;23(14):2074-9. doi: 10.1002/mds.22156. Mov Disord. 2008. PMID: 18785233

3

A novel LRRK2 mutation in a mainland Chinese patient with familial Parkinson's disease.

Wang L, Guo JF, Nie LL, Xu Q, Zuo X, Sun QY, Yan XX, Tang BS. Wang L, et al. Among authors: nie ll. Neurosci Lett. 2010 Jan 14;468(3):198-201. doi: 10.1016/j.neulet.2009.10.080. Epub 2009 Oct 29. Neurosci Lett. 2010. PMID: 19879329

4

A new variant of the ATP13A2 gene in Chinese patients with early-onset parkinsonism.

Wang L, Guo JF, Nie LL, Zhang HN, Shen L, Jiang H, Pan Q, Xia K, Tang BS, Yan XX. Wang L, et al. Among authors: nie ll. Chin Med J (Engl). 2009 Dec 20;122(24):3082-5. Chin Med J (Engl). 2009. PMID: 20137506 No abstract available.

5

Mutation analysis of Parkin, PINK1 and DJ-1 genes in Chinese patients with sporadic early onset parkinsonism.

Guo JF, Zhang XW, Nie LL, Zhang HN, Liao B, Li J, Wang L, Yan XX, Tang BS. Guo JF, et al. Among authors: nie ll. J Neurol. 2010 Jul;257(7):1170-5. doi: 10.1007/s00415-010-5485-8. Epub 2010 Feb 10. J Neurol. 2010. PMID: 20146068

6

[Establishment and application of an analytical method for PINK1 gene exon copy number].

Zhang HN, Liao B, Nie LL, Guo JE, Wang CY, Zhang XW, Yan XX, Tang BS. Zhang HN, et al. Among authors: nie ll. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Apr;27(2):158-61. doi: 10.3760/cma.j.issn.1003-9406.2010.02.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20376796 Chinese.

7

[DJ-1 gene rearrangement mutation in patients with autosomal recessive early-onset parkinsonism using real-time PCR].

Zhang H, Xiao B, Nie L, Guo J, Wang C, Wang L, He D, Yan X, Tang B. Zhang H, et al. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2010 May;35(5):438-44. doi: 10.3969/j.issn.1672-7347.2010.05.006. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2010. PMID: 20543466 Chinese.

8

Clinical features and [11C]-CFT PET analysis of PARK2, PARK6, PARK7-linked autosomal recessive early onset Parkinsonism.

Guo JF, Wang L, He D, Yang QH, Duan ZX, Zhang XW, Nie LL, Yan XX, Tang BS. Guo JF, et al. Among authors: nie ll. Neurol Sci. 2011 Feb;32(1):35-40. doi: 10.1007/s10072-010-0360-z. Epub 2010 Jul 7. Neurol Sci. 2011. PMID: 20607337

9

Case-control study of the UCH-L1 S18Y variant in sporadic Parkinson's disease in the Chinese population.

Wang L, Guo JF, Nie LL, Luo L, Zuo X, Shen L, Jiang H, Yan XX, Xia K, Pan Q, Tang BS. Wang L, et al. Among authors: nie ll. J Clin Neurosci. 2011 Apr;18(4):541-4. doi: 10.1016/j.jocn.2010.07.142. Epub 2011 Feb 18. J Clin Neurosci. 2011. PMID: 21315600

10

A new perspective on the current and future development potential of ABCG1.

Zeng GG, Lei Q, Jiang WL, Zhang XX, Nie L, Gong X, Zheng K. Zeng GG, et al. Curr Probl Cardiol. 2024 Jan;49(1 Pt C):102161. doi: 10.1016/j.cpcardiol.2023.102161. Epub 2023 Oct 22. Curr Probl Cardiol. 2024. PMID: 37875209 Review.

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