Lee CH - Search Results

1

Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver-Russell Syndrome.

Lin HY, Lee CL, Fran S, Tu RY, Chang YH, Niu DM, Chang CY, Chiu PC, Chou YY, Hsiao HP, Tsai MC, Chao MC, Tsai LP, Yang CF, Su PH, Pan YW, Lee CH, Chu TH, Chuang CK, Lin SP. Lin HY, et al. Among authors: lee ch, lee cl. J Pers Med. 2021 Nov 13;11(11):1197. doi: 10.3390/jpm11111197. J Pers Med. 2021. PMID: 34834549 Free PMC article.

2

Array-CGH increased the diagnostic rate of developmental delay or intellectual disability in Taiwan.

Lee CL, Lee CH, Chuang CK, Chiu HC, Chen YJ, Chou CL, Wu PS, Chen CP, Lin HY, Lin SP. Lee CL, et al. Among authors: lee ch. Pediatr Neonatol. 2019 Aug;60(4):453-460. doi: 10.1016/j.pedneo.2018.11.006. Epub 2018 Nov 27. Pediatr Neonatol. 2019. PMID: 30581099 Free article.

3

Critical Trio Exome Benefits In-Time Decision-Making for Pediatric Patients With Severe Illnesses.

Wu ET, Hwu WL, Chien YH, Hsu C, Chen TF, Chen NQ, Chou HC, Tsao PN, Fan PC, Tsai IJ, Lin SP, Hsieh WS, Chang TM, Chen CN, Lee CH, Chou YY, Chiu PC, Tsai WH, Hsiung HC, Lai F, Lee NC. Wu ET, et al. Among authors: lee ch, lee nc. Pediatr Crit Care Med. 2019 Nov;20(11):1021-1026. doi: 10.1097/PCC.0000000000002068. Pediatr Crit Care Med. 2019. PMID: 31261230

4

Newborn screening for Morquio disease and other lysosomal storage diseases: results from the 8-plex assay for 70,000 newborns.

Chien YH, Lee NC, Chen PW, Yeh HY, Gelb MH, Chiu PC, Chu SY, Lee CH, Lee AR, Hwu WL. Chien YH, et al. Among authors: lee nc, lee ch, lee ar. Orphanet J Rare Dis. 2020 Feb 3;15(1):38. doi: 10.1186/s13023-020-1322-z. Orphanet J Rare Dis. 2020. PMID: 32014045 Free PMC article.

5

Utility of whole-exome sequencing for patients with multiple congenital anomalies with or without intellectual disability/developmental delay in East Asia population.

Hsu RH, Lee CH, Chien YH, Lin SP, Hung MZ, Chen NC, Lin YL, Hwu WL, Lee NC. Hsu RH, et al. Among authors: lee ch, lee nc. Mol Genet Genomic Med. 2023 Jun;11(6):e2160. doi: 10.1002/mgg3.2160. Epub 2023 Feb 27. Mol Genet Genomic Med. 2023. PMID: 36849876 Free PMC article.

6

Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Silver-Russell Syndrome.

Lin HY, Lee CL, Tu YR, Chang YH, Niu DM, Chang CY, Chiu PC, Chou YY, Hsiao HP, Tsai MC, Chao MC, Tsai LP, Yang CF, Su PH, Pan YW, Lee CH, Chu TH, Chuang CK, Lin SP. Lin HY, et al. Among authors: lee ch, lee cl. Int J Med Sci. 2024 Jan 1;21(1):8-18. doi: 10.7150/ijms.84154. eCollection 2024. Int J Med Sci. 2024. PMID: 38164354 Free PMC article.

7

High Risk of Early Cataracts in Young Type 1 Diabetes Group: A Nationwide Cohort Study.

Lu WL, Shen PC, Lee CH, Su YT, Chen LM. Lu WL, et al. Among authors: lee ch. Int J Endocrinol. 2020 Oct 9;2020:8160256. doi: 10.1155/2020/8160256. eCollection 2020. Int J Endocrinol. 2020. PMID: 33133186 Free PMC article.

8

Maternal High-Fat Diet Controls Offspring Kidney Health and Disease.

Liu HY, Lee CH, Hsu CN, Tain YL. Liu HY, et al. Among authors: lee ch. Nutrients. 2023 Jun 9;15(12):2698. doi: 10.3390/nu15122698. Nutrients. 2023. PMID: 37375602 Free PMC article. Review.

9

Reply by Authors.

Selai C, Lee CH, Simeoni S, Pakzad M, Joyce E, Petrochilos P, Rantell KR, Boico V, Panicker JN. Selai C, et al. Among authors: lee ch. J Urol. 2024 May 11:101097JU0000000000004029. doi: 10.1097/JU.0000000000004029. Online ahead of print. J Urol. 2024. PMID: 38733281 No abstract available.

10

Epithelial-mesenchymal transition induced by tumor cell-intrinsic PD-L1 signaling predicts a poor response to immune checkpoint inhibitors in PD-L1-high lung cancer.

Jeong H, Koh J, Kim S, Song SG, Lee SH, Jeon Y, Lee CH, Keam B, Lee SH, Chung DH, Jeon YK. Jeong H, et al. Among authors: lee ch. Br J Cancer. 2024 May 10. doi: 10.1038/s41416-024-02698-4. Online ahead of print. Br J Cancer. 2024. PMID: 38729997

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