Soong BW - Search Results

1

Soong BW, Casamassima AC, Fink JK, Constantopoulos G, Horwitz AL. Soong BW, et al. Neurology. 1988 Aug;38(8):1273-5. doi: 10.1212/wnl.38.8.1273. Neurology. 1988. PMID: 2899861

2

Clinical spectrum of Niemann-Pick disease type C.

Fink JK, Filling-Katz MR, Sokol J, Cogan DG, Pikus A, Sonies B, Soong B, Pentchev PG, Comly ME, Brady RO, et al. Fink JK, et al. Neurology. 1989 Aug;39(8):1040-9. doi: 10.1212/wnl.39.8.1040. Neurology. 1989. PMID: 2761697

3

MPZ mutation G123S characterization: evidence for a complex pathogenesis in CMT disease.

Lee YC, Yu CT, Lin KP, Chang MH, Hsu SL, Liu YF, Lu YC, Soong BW. Lee YC, et al. Among authors: soong bw. Neurology. 2008 Jan 22;70(4):273-7. doi: 10.1212/01.wnl.0000296828.66915.bf. Neurology. 2008. PMID: 18209201

4

Gene symbol: MPZ. Disease: Charcot-Marie-Tooth disease type 1B.

Lee YC, Chang MH, Lin KP, Soong BW. Lee YC, et al. Among authors: soong bw. Hum Genet. 2005 Dec;118(3-4):547-8. Hum Genet. 2005. PMID: 16521307 No abstract available.

5

Dentatorubropallidoluysian atrophy in Chinese.

Lee IH, Soong BW, Lu YC, Chang YC. Lee IH, et al. Among authors: soong bw. Arch Neurol. 2001 Nov;58(11):1905-8. doi: 10.1001/archneur.58.11.1905. Arch Neurol. 2001. PMID: 11709002

6

An electrophysiologic and pathologic study of peripheral nerves in individuals with Machado-Joseph disease.

Soong BW, Lin KP. Soong BW, et al. Zhonghua Yi Xue Za Zhi (Taipei). 1998 Apr;61(4):181-7. Zhonghua Yi Xue Za Zhi (Taipei). 1998. PMID: 9614775

7

Correlation of peripheral nerve fiber loss and trinucleotide repeats in Machado-Joseph disease.

Soong BW, Lin KP. Soong BW, et al. Can J Neurol Sci. 1998 Feb;25(1):59-63. doi: 10.1017/s0317167100033503. Can J Neurol Sci. 1998. PMID: 9532283

8

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

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

9

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

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

10

Characterization of Heterozygous HTRA1 Mutations in Taiwanese Patients With Cerebral Small Vessel Disease.

Lee YC, Chung CP, Chao NC, Fuh JL, Chang FC, Soong BW, Liao YC. Lee YC, et al. Among authors: soong bw. Stroke. 2018 Jul;49(7):1593-1601. doi: 10.1161/STROKEAHA.118.021283. Epub 2018 Jun 12. Stroke. 2018. PMID: 29895533

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