Lee YC - Search Results

1

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. Ann Neurol. 2012 Dec;72(6):859-69. doi: 10.1002/ana.23701. Ann Neurol. 2012. PMID: 23280837 Free PMC article.

2

Prolonged cortical relay time of long latency reflex and central motor conduction in patients with spinocerebellar ataxia type 6.

Lee YC, Chen JT, Liao KK, Wu ZA, Soong BW. Lee YC, et al. Clin Neurophysiol. 2003 Mar;114(3):458-62. doi: 10.1016/s1388-2457(02)00378-4. Clin Neurophysiol. 2003. PMID: 12705426

3

Myelin protein zero gene mutations in Taiwanese patients with Charcot-Marie-Tooth disease type 1.

Lee YC, Soong BW, Lin KP, Lee HY, Wu ZA, Kao KP. Lee YC, et al. Among authors: lee hy. J Neurol Sci. 2004 Apr 15;219(1-2):95-100. doi: 10.1016/j.jns.2003.12.009. J Neurol Sci. 2004. PMID: 15050444

4

Prolonged central motor conduction time of lower limb muscle in spinocerebellar ataxia 6.

Chen JT, Lin YY, Lee YC, Soong BW, Wu ZA, Liao KK. Chen JT, et al. Among authors: lee yc. J Clin Neurosci. 2004 May;11(4):381-3. doi: 10.1016/j.jocn.2003.08.006. J Clin Neurosci. 2004. PMID: 15080952

5

Median nerve motor conduction velocity is concordant with myelin protein zero gene mutation.

Lee YC, Soong BW, Liu YT, Lin KP, Kao KP, Wu ZA. Lee YC, et al. J Neurol. 2005 Feb;252(2):151-5. doi: 10.1007/s00415-005-0621-6. J Neurol. 2005. PMID: 15729519

6

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: lee yc. Hum Genet. 2005 Feb;116(3):242. Hum Genet. 2005. PMID: 15818833 No abstract available.

7

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

Soong BW, Lee YC. Soong BW, et al. Among authors: lee yc. Hum Genet. 2005 Dec;118(3-4):543. Hum Genet. 2005. PMID: 16521289 No abstract available.

8

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. 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

9

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. 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

10

Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chinese.

Lee YC, Liu CS, Chang MH, Lin KP, Fuh JL, Lu YC, Liu YF, Soong BW. Lee YC, et al. J Neurol. 2009 Feb;256(2):249-55. doi: 10.1007/s00415-009-0091-3. Epub 2009 Feb 26. J Neurol. 2009. PMID: 19242647

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

5,654 results

Search Page

Filters