Lu YC - Search Results

1

SCA31 is rare in the Chinese population on Taiwan.

Lee YC, Liu CS, Lee TY, Lo YC, Lu YC, Soong BW. Lee YC, et al. Among authors: lu yc. Neurobiol Aging. 2012 Feb;33(2):426.e23-4. doi: 10.1016/j.neurobiolaging.2010.10.012. Epub 2010 Dec 15. Neurobiol Aging. 2012. PMID: 21163552

2

Common mitochondrial DNA and POLG1 mutations are rare in the Chinese patients with adult-onset ataxia on Taiwan.

Lee YC, Lu YC, Chang MH, Soong BW. Lee YC, et al. Among authors: lu yc. J Neurol Sci. 2007 Mar 15;254(1-2):65-8. doi: 10.1016/j.jns.2007.01.005. Epub 2007 Feb 14. J Neurol Sci. 2007. PMID: 17300808

3

Transmissible spongiform encephalopathies with P102L mutation of PRNP manifesting different phenotypes: clinical, neuroimaging, and electrophysiological studies in Chinese kindred in Taiwan.

Chi NF, Lee YC, Lu YC, Wu HM, Soong BW. Chi NF, et al. Among authors: lu yc. J Neurol. 2010 Feb;257(2):191-7. doi: 10.1007/s00415-009-5290-4. Epub 2009 Aug 21. J Neurol. 2010. PMID: 19696976

4

A hexanucleotide repeat expansion in C9ORF72 causes familial and sporadic ALS in Taiwan.

Tsai CP, Soong BW, Tu PH, Lin KP, Fuh JL, Tsai PC, Lu YC, Lee IH, Lee YC. Tsai CP, et al. Among authors: lu yc. Neurobiol Aging. 2012 Sep;33(9):2232.e11-2232.e18. doi: 10.1016/j.neurobiolaging.2012.05.002. Epub 2012 Jun 5. Neurobiol Aging. 2012. PMID: 22673113

5

Extensive molecular genetic survey of Taiwanese patients with amyotrophic lateral sclerosis.

Soong BW, Lin KP, Guo YC, Lin CC, Tsai PC, Liao YC, Lu YC, Wang SJ, Tsai CP, Lee YC. Soong BW, et al. Among authors: lu yc. Neurobiol Aging. 2014 Oct;35(10):2423.e1-6. doi: 10.1016/j.neurobiolaging.2014.05.008. Epub 2014 May 11. Neurobiol Aging. 2014. PMID: 24908169

6

A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23.

Chung MY, Lu YC, Cheng NC, Soong BW. Chung MY, et al. Among authors: lu yc. Brain. 2003 Jun;126(Pt 6):1293-9. doi: 10.1093/brain/awg130. Brain. 2003. PMID: 12764052

7

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: two novel mutations in the NOTCH3 gene in Chinese.

Lee YC, Yang AH, Liu HC, Wong WJ, Lu YC, Chang MH, Soong BW. Lee YC, et al. Among authors: lu yc. J Neurol Sci. 2006 Jul 15;246(1-2):111-5. doi: 10.1016/j.jns.2006.02.011. Epub 2006 Mar 31. J Neurol Sci. 2006. PMID: 16580020

8

Mutations in KCND3 cause spinocerebellar ataxia type 22.

Lee YC, Durr A, Majczenko K, Huang YH, Liu YC, Lien CC, Tsai PC, Ichikawa Y, Goto J, Monin ML, Li JZ, Chung MY, Mundwiller E, Shakkottai V, Liu TT, Tesson C, Lu YC, Brice A, Tsuji S, Burmeister M, Stevanin G, Soong BW. Lee YC, et al. Among authors: lu yc. Ann Neurol. 2012 Dec;72(6):859-69. doi: 10.1002/ana.23701. Ann Neurol. 2012. PMID: 23280837 Free PMC article.

9

Exome sequencing identifies GNB4 mutations as a cause of dominant intermediate Charcot-Marie-Tooth disease.

Soong BW, Huang YH, Tsai PC, Huang CC, Pan HC, Lu YC, Chien HJ, Liu TT, Chang MH, Lin KP, Tu PH, Kao LS, Lee YC. Soong BW, et al. Among authors: lu yc. Am J Hum Genet. 2013 Mar 7;92(3):422-30. doi: 10.1016/j.ajhg.2013.01.014. Epub 2013 Feb 21. Am J Hum Genet. 2013. PMID: 23434117 Free PMC article.

10

Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Soong BW, Lee YC, Lu YC. Soong BW, et al. Among authors: lu yc. Hum Genet. 2005 Feb;116(3):242. Hum Genet. 2005. PMID: 15818833 No abstract available.

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

Text availability

Article attribute

Article type

Publication date

1,072 results

Search Page