Lai KL - 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: lai kl. 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

Fatigue as the only clinical manifestation of colchicine induced myopathy.

Lo YC, Lin KP, Lin CY, Kao CD, Chen JT, Lai KL, Lin YY, Lee YC, Liao KK. Lo YC, et al. Among authors: lai kl. Acta Neurol Taiwan. 2010 Sep;19(3):184-8. Acta Neurol Taiwan. 2010. PMID: 20824538

3

"Effect of transcranial magnetic stimulation to motor cortex on pain perception and nociceptive reflex".

Lin KP, Liao KK, Lai KL, Lin YY, Chiou SY, Wu ZA. Lin KP, et al. Among authors: lai kl. Chin J Physiol. 2012 Jun 30;55(3):163-8. doi: 10.4077/CJP.2012.AMM117. Chin J Physiol. 2012. PMID: 22784280

4

Paired nociceptive blink stimuli can facilitate trigeminofacial circuit at a long inter-stimulus interval.

Tsao YC, Lai KL, Chen JT, Liao KK, Wang SJ. Tsao YC, et al. Among authors: lai kl. J Chin Med Assoc. 2019 Jan;82(1):30-34. doi: 10.1097/JCMA.0000000000000003. J Chin Med Assoc. 2019. PMID: 30839400

5

Investigating PUM1 mutations in a Taiwanese cohort with cerebellar ataxia.

Lai KL, Liao YC, Tsai PC, Hsiao CT, Soong BW, Lee YC. Lai KL, et al. Parkinsonism Relat Disord. 2019 Sep;66:220-223. doi: 10.1016/j.parkreldis.2019.08.004. Epub 2019 Aug 7. Parkinsonism Relat Disord. 2019. PMID: 31422002

6

Clinical and genetic characterization of adult-onset leukoencephalopathy caused by CSF1R mutations.

Tsai PC, Fuh JL, Yang CC, Chang A, Lien LM, Wang PN, Lai KL, Tsai YS, Lee YC, Liao YC. Tsai PC, et al. Among authors: lai kl. Ann Clin Transl Neurol. 2021 Nov;8(11):2121-2131. doi: 10.1002/acn3.51467. Epub 2021 Oct 15. Ann Clin Transl Neurol. 2021. PMID: 34652888 Free PMC article.

7

Mutation screening and association analysis of NOTCH3 p.R544C in patients with migraine with or without aura.

Wang YF, Liao YC, Tzeng YS, Chen SP, Lirng JF, Fuh JL, Chen WT, Lai KL, Lee YC, Wang SJ. Wang YF, et al. Among authors: lai kl. Cephalalgia. 2022 Aug;42(9):888-898. doi: 10.1177/03331024221080891. Epub 2022 Mar 18. Cephalalgia. 2022. PMID: 35302383

8

Clinical and genetic characterization of NEFL-related neuropathy in Taiwan.

Chao HC, Hsiao CT, Lai KL, Tsai YS, Lin KP, Liao YC, Lee YC. Chao HC, et al. Among authors: lai kl. J Formos Med Assoc. 2023 Feb;122(2):132-138. doi: 10.1016/j.jfma.2022.08.008. Epub 2022 Aug 26. J Formos Med Assoc. 2023. PMID: 36031490 Free article.

9

Transient visual disturbances are associated with disability and suicide risk in patients with migraine without aura.

Tsao YC, Wang YF, Fuh JL, Chen WT, Lai KL, Liu HY, Wang SJ, Chen SP. Tsao YC, et al. Among authors: lai kl. J Chin Med Assoc. 2023 Jun 1;86(6):557-564. doi: 10.1097/JCMA.0000000000000912. Epub 2023 Mar 13. J Chin Med Assoc. 2023. PMID: 36907842

10

Identification of m.3243A>G mitochondrial DNA mutation in patients with cerebellar ataxia.

Liao NY, Lai KL, Liao YC, Hsiao CT, Lee YC. Liao NY, et al. Among authors: lai kl. J Formos Med Assoc. 2023 Oct;122(10):1028-1034. doi: 10.1016/j.jfma.2023.05.031. Epub 2023 Jun 11. J Formos Med Assoc. 2023. PMID: 37311680 Free article.

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