Chu TH - 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: chu th. J Pers Med. 2021 Nov 13;11(11):1197. doi: 10.3390/jpm11111197. J Pers Med. 2021. PMID: 34834549 Free PMC article.

2

Very Early Treatment for Infantile-Onset Pompe Disease Contributes to Better Outcomes.

Yang CF, Yang CC, Liao HC, Huang LY, Chiang CC, Ho HC, Lai CJ, Chu TH, Yang TF, Hsu TR, Soong WJ, Niu DM. Yang CF, et al. Among authors: chu th. J Pediatr. 2016 Feb;169:174-80.e1. doi: 10.1016/j.jpeds.2015.10.078. Epub 2015 Dec 10. J Pediatr. 2016. PMID: 26685070

3

Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith-Wiedemann syndrome.

Lin HY, Chuang CK, Tu RY, Fang YY, Su YN, Chen CP, Chang CY, Liu HC, Chu TH, Niu DM, Lin SP. Lin HY, et al. Among authors: chu th. Mol Genet Metab. 2016 Sep;119(1-2):8-13. doi: 10.1016/j.ymgme.2016.07.003. Epub 2016 Jul 12. Mol Genet Metab. 2016. PMID: 27436784

4

Later Onset Fabry Disease, Cardiac Damage Progress in Silence: Experience With a Highly Prevalent Mutation.

Hsu TR, Hung SC, Chang FP, Yu WC, Sung SH, Hsu CL, Dzhagalov I, Yang CF, Chu TH, Lee HJ, Lu YH, Chang SK, Liao HC, Lin HY, Liao TC, Lee PC, Li HY, Yang AH, Ho HC, Chiang CC, Lin CY, Desnick RJ, Niu DM. Hsu TR, et al. Among authors: chu th. J Am Coll Cardiol. 2016 Dec 13;68(23):2554-2563. doi: 10.1016/j.jacc.2016.09.943. J Am Coll Cardiol. 2016. PMID: 27931613 Free article.

5

Correlations between Endomyocardial Biopsies and Cardiac Manifestations in Taiwanese Patients with the Chinese Hotspot IVS4+919G>A Mutation: Data from the Fabry Outcome Survey.

Hsu TR, Chang FP, Chu TH, Sung SH, Bizjajeva S, Yu WC, Niu DM. Hsu TR, et al. Among authors: chu th. Int J Mol Sci. 2017 Jan 9;18(1):119. doi: 10.3390/ijms18010119. Int J Mol Sci. 2017. PMID: 28075357 Free PMC article.

6

A comparison of central nervous system involvement in patients with classical Fabry disease or the later-onset subtype with the IVS4+919G>A mutation.

Lee HJ, Hsu TR, Hung SC, Yu WC, Chu TH, Yang CF, Bizjajeva S, Tiu CM, Niu DM. Lee HJ, et al. Among authors: chu th. BMC Neurol. 2017 Feb 6;17(1):25. doi: 10.1186/s12883-017-0810-9. BMC Neurol. 2017. PMID: 28166746 Free PMC article.

7

Experiences during newborn screening for glutaric aciduria type 1: Diagnosis, treatment, genotype, phenotype, and outcomes.

Tsai FC, Lee HJ, Wang AG, Hsieh SC, Lu YH, Lee MC, Pai JS, Chu TH, Yang CF, Hsu TR, Lai CJ, Tsai MT, Ho PH, Lin MC, Cheng LY, Chuang YC, Niu DM. Tsai FC, et al. Among authors: chu th. J Chin Med Assoc. 2017 Apr;80(4):253-261. doi: 10.1016/j.jcma.2016.07.006. Epub 2017 Mar 13. J Chin Med Assoc. 2017. PMID: 28302372 Free article.

8

Methylmalonic acidemia/propionic acidemia - the biochemical presentation and comparing the outcome between liver transplantation versus non-liver transplantation groups.

Chu TH, Chien YH, Lin HY, Liao HC, Ho HJ, Lai CJ, Chiang CC, Lin NC, Yang CF, Hwu WL, Lee NC, Lin SP, Liu CS, Hu RH, Ho MC, Niu DM. Chu TH, et al. Orphanet J Rare Dis. 2019 Apr 2;14(1):73. doi: 10.1186/s13023-019-1045-1. Orphanet J Rare Dis. 2019. PMID: 30940196 Free PMC article.

9

Very rare condition of multiple Gaucheroma: A case report and review of the literature.

Tseng SY, Niu DM, Chu TH, Yeh YC, Huang MH, Yang TF, Liao HC, Chiang CC, Ho HC, Soong WJ, Yang CF. Tseng SY, et al. Among authors: chu th. Mol Genet Metab Rep. 2019 May 9;20:100473. doi: 10.1016/j.ymgmr.2019.100473. eCollection 2019 Sep. Mol Genet Metab Rep. 2019. PMID: 31193028 Free PMC article.

10

Very rare condition of multiple Gaucheroma: A case report and review of the literature.

Tseng SY, Niu DM, Chu TH, Yeh YC, Huang MH, Yang TF, Liao HC, Chiang CC, Ho HC, Soong WJ, Yang CF. Tseng SY, et al. Among authors: chu th. Mol Genet Metab Rep. 2019 Jul 12;20:100489. doi: 10.1016/j.ymgmr.2019.100489. eCollection 2019 Sep. Mol Genet Metab Rep. 2019. PMID: 31341788 Free PMC article.

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