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臨床試驗主持人



更新時間:2023-09-19

鄭惠禎Cheng, Hui-Chen
  • 協同主持人
  • 執行臨床試驗年資
  • hccheng7@vghtpe.gov.tw

發表文獻

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21

Yeh HJ, Chen TA, Cheng HC, et al. Long-Term Rehabilitation Utilization Pattern Among Stroke Patients Under the National Health Insurance Program. Am J Phys Med Rehabil 2022;101:129-34

22

Wu RY, Sung WH, Cheng HC, Yeh HJ. Investigating the rate of skeletal muscle atrophy in men and women in the intensive care unit: a prospective observational study. Sci Rep. 2022;12(1):16629.

23

Cheng HC, Chi SC, Liang CY, Yu JY, Wang AG. Candidate Modifier Genes for the Penetrance of Leber's Hereditary Optic Neuropathy. Int J Mol Sci. 2022;23(19).

24

Hung WC, Cheng HC, Wang AG. Melanoma-associated retinopathy with anti-TRPM1 autoantibodies showing concomitant Off-bipolar cell dysfunction. Doc Ophthalmol. 2022;145(3):263-70.

25

Yeh TC, Cheng HC#, Li HY, Chi SC, Yang HY, Yu JY, et al. Ophthalmic characteristics and retinal vasculature changes in Williams syndrome, and its association with systemic diseases. Eye (Lond). 2023;37:2265-2271..( #co-first author)

26

Chi SC, Cheng HC#, Wang AG. Leber Hereditary Optic Neuropathy: Molecular Pathophysiology and Updates on Gene Therapy. Biomedicines. 2022;10(8). (#co-first author)

27

Yeh TC, Niu DM, Cheng HC, Chen YR, Chen LZ, Tsui SP, et al. Novel mutation of IFT140 in an infant with Mainzer-Saldino syndrome presenting with retinal dystrophy. Mol Genet Metab Rep. 2022;33:100937.
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