Soong BW - Search Results

1

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: soong bw. 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

2

Metabolic characterization of spinocerebellar ataxia type 6.

Soong B, Liu R, Wu L, Lu Y, Lee H. Soong B, et al. Arch Neurol. 2001 Feb;58(2):300-4. doi: 10.1001/archneur.58.2.300. Arch Neurol. 2001. PMID: 11176970 Clinical Trial.

3

5'-flanking region polymorphism of the neuronal nitric oxide synthase gene with Parkinson's disease in Taiwan.

Lo HS, Hogan EL, Soong BW. Lo HS, et al. Among authors: soong bw. J Neurol Sci. 2002 Feb 15;194(1):11-3. doi: 10.1016/s0022-510x(01)00666-9. J Neurol Sci. 2002. PMID: 11809160

4

Peripheral neuropathy of Machado-Joseph disease in Taiwan: a morphometric and genetic study.

Lin KP, Soong BW. Lin KP, et al. Among authors: soong bw. Eur Neurol. 2002;48(4):210-7. doi: 10.1159/000066169. Eur Neurol. 2002. PMID: 12422070

5

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. Among authors: soong bw. Clin Neurophysiol. 2003 Mar;114(3):458-62. doi: 10.1016/s1388-2457(02)00378-4. Clin Neurophysiol. 2003. PMID: 12705426

6

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: soong bw. J Clin Neurosci. 2004 May;11(4):381-3. doi: 10.1016/j.jocn.2003.08.006. J Clin Neurosci. 2004. PMID: 15080952

7

Congenital insensitivity to pain with anhidrosis in Taiwan: a morphometric and genetic study.

Guo YC, Liao KK, Soong BW, Tsai CP, Niu DM, Lee HY, Lin KP. Guo YC, et al. Among authors: soong bw. Eur Neurol. 2004;51(4):206-14. doi: 10.1159/000078487. Epub 2004 May 17. Eur Neurol. 2004. PMID: 15159601

8

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. Among authors: soong bw. J Neurol. 2005 Feb;252(2):151-5. doi: 10.1007/s00415-005-0621-6. J Neurol. 2005. PMID: 15729519

9

Allele-specific all-or-none PCR product diagnostic strategy for Charcot-Marie-Tooth 1A and hereditary neuropathy with liability to pressure palsies.

Lin KP, Chou CH, Lee HY, Soong BW. Lin KP, et al. Among authors: soong bw. J Chin Med Assoc. 2006 Feb;69(2):68-73. doi: 10.1016/S1726-4901(09)70116-9. J Chin Med Assoc. 2006. PMID: 16570573 Free article.

10

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: soong bw. 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

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