Jih KY - 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. 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

Nerve conduction features may serve as a diagnostic clue for neuronal intranuclear inclusion disease.

Jih KY, Lan MY, Liu YH, Tsai YS, Lin PY, Lai KL, Liao YC, Lee YC. Jih KY, et al. Brain Commun. 2024 Jun 26;6(4):fcae221. doi: 10.1093/braincomms/fcae221. eCollection 2024. Brain Commun. 2024. PMID: 38978725 Free PMC article.

3

TBK1 p.Y153Qfs*9 variant may be associated with young-onset, rapidly progressive amyotrophic lateral sclerosis through a haploinsufficiency mechanism.

Fang SY, Tsai PC, Jih KY, Hsu FC, Liao YC, Yang CC, Lee YC. Fang SY, et al. Among authors: jih ky. J Chin Med Assoc. 2024 Oct 1;87(10):920-926. doi: 10.1097/JCMA.0000000000001147. Epub 2024 Aug 9. J Chin Med Assoc. 2024. PMID: 39118204

4

The role of adiponectin-AMPK axis in TDP-43 mislocalization and disease severity in ALS.

Liu YJ, Lee CW, Liao YC, Huang JJ, Kuo HC, Jih KY, Lee YC, Chern Y. Liu YJ, et al. Among authors: jih ky. Neurobiol Dis. 2024 Nov;202:106715. doi: 10.1016/j.nbd.2024.106715. Epub 2024 Oct 28. Neurobiol Dis. 2024. PMID: 39490684 Free article.

5

Investigating ITM2B-associated ataxia in a Taiwanese cerebellar ataxia cohort.

Fang SY, Hsiao CT, Jih KY, Tsai YS, Lai KL, Chou CT, Liao YC, Lee YC. Fang SY, et al. Among authors: jih ky. Ann Clin Transl Neurol. 2024 Dec 3. doi: 10.1002/acn3.52265. Online ahead of print. Ann Clin Transl Neurol. 2024. PMID: 39625954 Free article.

6

Assessing the NOTCH2NLC GGC repeat expansion in Taiwanese patients with hereditary spastic paraplegia.

Hsu SL, Jih KY, Lin KP, Liao YC, Lee YC. Hsu SL, et al. Among authors: jih ky. Parkinsonism Relat Disord. 2022 Mar;96:43-44. doi: 10.1016/j.parkreldis.2022.02.004. Epub 2022 Feb 13. Parkinsonism Relat Disord. 2022. PMID: 35180462

7

Genetic and Functional Analysis of Glycosyltransferase 8 Domain-Containing Protein 1 in Taiwanese Patients With Amyotrophic Lateral Sclerosis.

Tsai PC, Jih KY, Shen TY, Liu YH, Lin KP, Liao YC, Lee YC. Tsai PC, et al. Among authors: jih ky. Neurol Genet. 2021 Nov 3;7(6):e627. doi: 10.1212/NXG.0000000000000627. eCollection 2021 Dec. Neurol Genet. 2021. PMID: 34746377 Free PMC article.

8

GGC Repeat Expansion of NOTCH2NLC in Taiwanese Patients With Inherited Neuropathies.

Liao YC, Chang FP, Huang HW, Chen TB, Chou YT, Hsu SL, Jih KY, Liu YH, Hsiao CT, Fukukda H, Mizuguchi T, Lin KP, Lin CK, Matsumoto N, Kennerson M, Lee YC. Liao YC, et al. Among authors: jih ky. Neurology. 2022 Jan 11;98(2):e199-e206. doi: 10.1212/WNL.0000000000013008. Epub 2021 Oct 21. Neurology. 2022. PMID: 34675106

9

Analysis of NOTCH2NLC GGC repeat expansion in Taiwanese patients with amyotrophic lateral sclerosis.

Jih KY, Chou YT, Tsai PC, Liao YC, Lee YC. Jih KY, et al. Neurobiol Aging. 2021 Dec;108:210-212. doi: 10.1016/j.neurobiolaging.2021.07.011. Epub 2021 Jul 23. Neurobiol Aging. 2021. PMID: 34392981

10

Investigating TBP CAG/CAA trinucleotide repeat expansions in a Taiwanese cohort with ALS.

Jih KY, Lin KP, Tsai PC, Soong BW, Liao YC, Lee YC. Jih KY, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2021 Aug;22(5-6):442-447. doi: 10.1080/21678421.2020.1867182. Epub 2020 Dec 30. Amyotroph Lateral Scler Frontotemporal Degener. 2021. PMID: 33377399

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

25 results

Search Page

Filters