Lee YC - Search Results

1

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.

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

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

8

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

9

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

10

The remarkably variable expressivity of CADASIL: report of a minimally symptomatic man at an advanced age.

Lee YC, Yang AH, Soong BW. Lee YC, et al. J Neurol. 2009 Jun;256(6):1026-7. doi: 10.1007/s00415-009-5048-z. Epub 2009 Mar 1. J Neurol. 2009. PMID: 19252787 No abstract available.

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