Yu-Wen Pan - Search Results

Year	Number of Results
2019	1
2020	1
2021	3
2022	2
2023	4
2024	2

1

Enzyme replacement therapy for children with acid sphingomyelinase deficiency in the real world: A single center experience in Taiwan.

Pan YW, Tsai MC, Yang CY, Yu WH, Wang B, Yang YJ, Chou YY. Pan YW, et al. Mol Genet Metab Rep. 2023 Jan 31;34:100957. doi: 10.1016/j.ymgmr.2023.100957. eCollection 2023 Mar. Mol Genet Metab Rep. 2023. PMID: 36873248 Free PMC article.

2

Syndromic ciliopathy: a taiwanese single-center study.

Pan YW, Ou TY, Chou YY, Kuo PL, Hsiao HP, Chiu PC, Lin JL, Lo FS, Wang CH, Chen PC, Tsai MC. Pan YW, et al. BMC Med Genomics. 2024 Apr 26;17(1):106. doi: 10.1186/s12920-024-01880-0. BMC Med Genomics. 2024. PMID: 38671463 Free PMC article.

3

Postnatal Serum Total Thyroxine Level Associated with Short- and Long-Term Anthropometric Outcomes in Very Preterm Infants.

Chen YJ, Chu WY, Pan YW, Wang CY, Chou YY, Lin CH, Tsuda K, Iwata O, Yu WH, Lin YC. Chen YJ, et al. Among authors: pan yw. Nutrients. 2022 May 14;14(10):2056. doi: 10.3390/nu14102056. Nutrients. 2022. PMID: 35631197 Free PMC article.

4

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: pan yw. J Pers Med. 2021 Nov 13;11(11):1197. doi: 10.3390/jpm11111197. J Pers Med. 2021. PMID: 34834549 Free PMC article.

5

Postnatal Serum Total Thyroxine of Very Preterm Infants and Long-Term Neurodevelopmental Outcome.

Lin YC, Wang CY, Pan YW, Chen YJ, Yu WH, Chou YY, Huang CH, Chu WY, Lin CH, Iwata O. Lin YC, et al. Among authors: pan yw. Nutrients. 2021 Mar 24;13(4):1055. doi: 10.3390/nu13041055. Nutrients. 2021. PMID: 33805038 Free PMC article.

6

Segmental isodisomy in Prader-Willi syndrome patients: The experience of a single diagnostic center.

Pan YW, Chang CW, Jong YJ, Chou YY, Kuo PL. Pan YW, et al. Pediatr Neonatol. 2020 Jun;61(3):343-345. doi: 10.1016/j.pedneo.2020.02.007. Epub 2020 Feb 21. Pediatr Neonatol. 2020. PMID: 32192873 Free article. No abstract available.

7

Congenital hypothyroidism as the initial presentation of pendred syndrome associated with mutated IVS7-2A>G in SLC26A4 gene in a Taiwanese neonate.

Chung SM, Pan YW, Tsai YS, Tsai MC. Chung SM, et al. Among authors: pan yw. Pediatr Neonatol. 2023 Jan;64(1):94-95. doi: 10.1016/j.pedneo.2022.06.008. Epub 2022 Sep 8. Pediatr Neonatol. 2023. PMID: 36154804 Free article. No abstract available.

8

A boy with a progressive neurologic decline harboring two coexisting mutations in KMT2D and VPS13D.

Chang YM, Pan YW, Chou YY, Yu WH, Tsai MC. Chang YM, et al. Among authors: pan yw. Brain Dev. 2023 Nov;45(10):603-607. doi: 10.1016/j.braindev.2023.08.001. Epub 2023 Aug 18. Brain Dev. 2023. PMID: 37599126

9

The relationship between nonalcoholic fatty liver disease and pediatric congenital hypothyroidism patients.

Pan YW, Tsai MC, Yang YJ, Chen MY, Chen SY, Chou YY. Pan YW, et al. Kaohsiung J Med Sci. 2019 Dec;35(12):778-786. doi: 10.1002/kjm2.12118. Epub 2019 Aug 9. Kaohsiung J Med Sci. 2019. PMID: 31400075 Free article.

10

Correlates of disordered eating and insulin restriction behavior and its association with psychological health in Taiwanese youths with diabetes mellitus.

Chou WC, Chou YY, Pan YW, Ou TY, Tsai MC. Chou WC, et al. Among authors: pan yw. J Eat Disord. 2023 Sep 14;11(1):158. doi: 10.1186/s40337-023-00888-8. J Eat Disord. 2023. PMID: 37710329 Free PMC article.

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