Lin KP - Search Results

1

Reduced-penetrance Huntington's disease-causing alleles with 39 CAG trinucleotide repeats could be a genetic factor of amyotrophic lateral sclerosis.

Jih KY, Lai KL, Lin KP, Liao YC, Lee YC. Jih KY, et al. Among authors: lin kp. J Chin Med Assoc. 2023 Jan 1;86(1):47-51. doi: 10.1097/JCMA.0000000000000837. Epub 2022 Nov 28. J Chin Med Assoc. 2023. PMID: 36599142

2

Wernicke's encephalopathy in a patient with multiple symmetrical lipomatosis and the A8344G mutation of mitochondrial DNA.

Lee YC, Wei YH, Lirng JF, Lee HC, Tso DJ, Lin KP, Wu ZA, Liu HC. Lee YC, et al. Among authors: lin kp. Eur Neurol. 2002;47(2):126-8. doi: 10.1159/000047967. Eur Neurol. 2002. PMID: 11844905 No abstract available.

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: lin kp. 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

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: lin kp. J Neurol. 2005 Feb;252(2):151-5. doi: 10.1007/s00415-005-0621-6. J Neurol. 2005. PMID: 15729519

5

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. 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.

6

Transthyretin Ala97Ser in Chinese-Taiwanese patients with familial amyloid polyneuropathy: genetic studies and phenotype expression.

Liu YT, Lee YC, Yang CC, Chen ML, Lin KP. Liu YT, et al. Among authors: lin kp. J Neurol Sci. 2008 Apr 15;267(1-2):91-9. doi: 10.1016/j.jns.2007.10.011. Epub 2007 Nov 26. J Neurol Sci. 2008. PMID: 18022643

7

[Charcot-Marie-Tooth disease].

Lee YC, Chang MH, Lin KP. Lee YC, et al. Among authors: lin kp. Acta Neurol Taiwan. 2008 Sep;17(3):203-13. Acta Neurol Taiwan. 2008. PMID: 18975529 Review. Chinese.

8

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. Among authors: lin kp. J Neurol. 2009 Feb;256(2):249-55. doi: 10.1007/s00415-009-0091-3. Epub 2009 Feb 26. J Neurol. 2009. PMID: 19242647

9

Cellular characterization of MPZ mutations presenting with diverse clinical phenotypes.

Lee YC, Lin KP, Chang MH, Liao YC, Tsai CP, Liao KK, Soong BW. Lee YC, et al. Among authors: lin kp. J Neurol. 2010 Oct;257(10):1661-8. doi: 10.1007/s00415-010-5590-8. Epub 2010 May 12. J Neurol. 2010. PMID: 20461396

10

FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS.

Tsai CP, Soong BW, Lin KP, Tu PH, Lin JL, Lee YC. Tsai CP, et al. Among authors: lin kp, lin jl. Neurobiol Aging. 2011 Mar;32(3):553.e13-21. doi: 10.1016/j.neurobiolaging.2010.04.009. Epub 2010 May 15. Neurobiol Aging. 2011. PMID: 20472325

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