Kim YE - Search Results

1

PSEN1 variants in Korean patients with clinically suspicious early-onset familial Alzheimer's disease.

Kim YE, Cho H, Kim HJ, Na DL, Seo SW, Ki CS. Kim YE, et al. Among authors: kim hj. Sci Rep. 2020 Feb 26;10(1):3480. doi: 10.1038/s41598-020-59829-z. Sci Rep. 2020. PMID: 32103039 Free PMC article.

2

A novel mutation (c.200T>C) in the NAGLU gene of a Korean patient with mucopolysaccharidosis IIIB.

Kim YE, Park HD, Jang MA, Ki CS, Lee SY, Kim JW, Cho SY, Jin DK. Kim YE, et al. Among authors: kim jw. Ann Lab Med. 2013 May;33(3):221-4. doi: 10.3343/alm.2013.33.3.221. Epub 2013 Apr 17. Ann Lab Med. 2013. PMID: 23667853 Free PMC article.

3

Parkin mutation and deep brain stimulation outcome.

Kim HJ, Yun JY, Kim YE, Lee JY, Kim HJ, Kim JY, Park SS, Paek SH, Jeon BS. Kim HJ, et al. Among authors: kim jy, kim ye. J Clin Neurosci. 2014 Jan;21(1):107-10. doi: 10.1016/j.jocn.2013.03.026. Epub 2013 Sep 21. J Clin Neurosci. 2014. PMID: 24060625

4

Spectrum of NOTCH3 mutations in Korean patients with clinically suspicious cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Kim YE, Yoon CW, Seo SW, Ki CS, Kim YB, Kim JW, Bang OY, Lee KH, Kim GM, Chung CS, Na DL. Kim YE, et al. Among authors: kim gm, kim yb, kim jw. Neurobiol Aging. 2014 Mar;35(3):726.e1-6. doi: 10.1016/j.neurobiolaging.2013.09.004. Epub 2013 Oct 16. Neurobiol Aging. 2014. PMID: 24139282

5

De novo FUS mutations in 2 Korean patients with sporadic amyotrophic lateral sclerosis.

Kim YE, Oh KW, Kwon MJ, Choi WJ, Oh SI, Ki CS, Kim SH. Kim YE, et al. Among authors: kim sh. Neurobiol Aging. 2015 Mar;36(3):1604.e17-9. doi: 10.1016/j.neurobiolaging.2014.10.002. Epub 2014 Oct 13. Neurobiol Aging. 2015. PMID: 25457557

6

Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a mutation in the arginine-vasopressin II gene in four generations of a Korean family.

Kim MJ, Kim YE, Ki CS, Yoo JH. Kim MJ, et al. Among authors: kim ye. Ann Pediatr Endocrinol Metab. 2014 Dec;19(4):220-4. doi: 10.6065/apem.2014.19.4.220. Epub 2014 Dec 31. Ann Pediatr Endocrinol Metab. 2014. PMID: 25654069 Free PMC article.

7

NOTCH3 variants in patients with subcortical vascular cognitive impairment: a comparison with typical CADASIL patients.

Yoon CW, Kim YE, Seo SW, Ki CS, Choi SH, Kim JW, Na DL. Yoon CW, et al. Among authors: kim ye, kim jw. Neurobiol Aging. 2015 Aug;36(8):2443.e1-7. doi: 10.1016/j.neurobiolaging.2015.04.009. Epub 2015 Apr 25. Neurobiol Aging. 2015. PMID: 26002683

8

Identification of mutations in Korean patients with amyotrophic lateral sclerosis using multigene panel testing.

Kim HJ, Oh KW, Kwon MJ, Oh SI, Park JS, Kim YE, Choi BO, Lee S, Ki CS, Kim SH. Kim HJ, et al. Among authors: kim sh, kim ye. Neurobiol Aging. 2016 Jan;37:209.e9-209.e16. doi: 10.1016/j.neurobiolaging.2015.09.012. Epub 2015 Sep 30. Neurobiol Aging. 2016. PMID: 26601740

9

Directly converted patient-specific induced neurons mirror the neuropathology of FUS with disrupted nuclear localization in amyotrophic lateral sclerosis.

Lim SM, Choi WJ, Oh KW, Xue Y, Choi JY, Kim SH, Nahm M, Kim YE, Lee J, Noh MY, Lee S, Hwang S, Ki CS, Fu XD, Kim SH. Lim SM, et al. Among authors: kim sh, kim ye. Mol Neurodegener. 2016 Jan 22;11:8. doi: 10.1186/s13024-016-0075-6. Mol Neurodegener. 2016. PMID: 26795035 Free PMC article.

10

CLEC4C p.K210del variant causes impaired cell surface transport in plasmacytoid dendritic cells of amyotrophic lateral sclerosis.

Lim SM, Kim YE, Choi WJ, Oh KW, Noh MY, Kwon MS, Nahm M, Kim N, Ki CS, Kim SH. Lim SM, et al. Among authors: kim sh, kim n, kim ye. Oncotarget. 2016 May 3;7(18):24942-9. doi: 10.18632/oncotarget.7886. Oncotarget. 2016. PMID: 26943047 Free PMC article.

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