Ming-Hui Sun

Dr. Ming-Hui Sun

orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 April 2019 in Eye
Verified
Journal Article
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YFYuan-Yao Fan
Yuan-Yao Fan
WSWei-Wen Su
Wei-Wen Su
CLChun-Hsiu Liu
Chun-Hsiu Liu
HCHenry Shen-Lih Chen
Henry Shen-Lih Chen
SWShiu-Chen Wu
Shiu-Chen Wu
MSMing-Hui Sun
Ming-Hui Sun


25 August 2014 in Chemical Communications
Verified
Journal Article
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JCJie Chen
Jie Chen
YGYu-Ping Guo
Yu-Ping Guo
MSMing-Hui Sun
Ming-Hui Sun
GFGuo-Tao Fan
Guo-Tao Fan
LZLing Zhou
Ling Zhou
A new bromoform reaction of tertiary amines with N,N-dibromosulfonamides or NBS/sulfonamides has been developed. A series of amidines were prepared with moderate to good yields via a Csp3–Csp3 bond cleavage.

24 November 2014 in BMC Ophthalmology
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Journal Article
Open access
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Yi-Hsing ChenYi-Hsing Chen
Yi-Hsing Chen
MSMing-Hui Sun
Ming-Hui Sun
SHShao-Hsuan Hsia
Shao-Hsuan Hsia
CLChi-Chun Lai
Chi-Chun Lai
Wei-Chi WuWei-Chi Wu
Wei-Chi Wu
Background: Kabuki syndrome is a multi-system disorder with peculiar facial features, and ophthalmic abnormalities are frequently involved. This case report of a child with Kabuki syndrome describes two new previously unreported ophthalmic conditions. Case presentation: A 3-year-old Taiwanese boy with Kabuki syndrome had a short stature, spinal dysraphism, intellectual disability and typical facial features. Ophthalmic findings which have been previously reported in the literature and in this patient, included ptosis, esotropia, coloboma of the iris, retina, choroid and optic disc, and microcornea. The newly identified ophthalmic features in this patient included colobomatous microphthalmos and a dysplastic and elevated disc without central cupping. The genetic analysis identified an MLL2 gene mutation. Conclusion: The presentations of a dysplastic disc and colobomatous microphthalmia are rarely reported in patients with Kabuki syndrome, but these ophthalmic abnormalities may affect vision. Detailed ophthalmic evaluations in children with Kabuki syndrome are advised.

1 June 2021 in American Journal of Ophthalmology
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Journal Article
Closed access
JCJui-Fan Chiang
Jui-Fan Chiang
MSMing-Hui Sun
Ming-Hui Sun
KCKuan-Jen Chen
Kuan-Jen Chen
WWWei-Chi Wu
Wei-Chi Wu
CLChi-Chun Lai
Chi-Chun Lai
HLHsueh-Yu Li
Hsueh-Yu Li

16 June 2022 in Journal of Fungi
Verified
Journal Article
Open access
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KCKuan-Jen Chen
Kuan-Jen Chen
MSMing-Hui Sun
Ming-Hui Sun
YCYen-Po Chen
Yen-Po Chen
Yi-Hsing ChenYi-Hsing Chen
Yi-Hsing Chen
Nan-Kai WangNan-Kai Wang
Nan-Kai Wang
CLChi-Chun Lai
Chi-Chun Lai
Endogenous fungal endophthalmitis (EFE) is a vision-threatening intraocular infection and a rare complication of fungemia. Early diagnosis and prompt aggressive treatment are crucial to avoid vision loss. We retrospectively reviewed the data of 37 patients (49 eyes) with EFE who were treated at a tertiary referral hospital from January 2000 to April 2019. The most common risk factor was diabetes (24 patients; 65%), followed by recent hospitalization, urinary tract disease, liver disease, and immunosuppressive therapy. Two or more risk factors were detected in 24 patients (65%), and yeasts (29 patients; 78%) were more commonly detected than mold (8 patients; 22%). The most common fungal isolates were Candida spp. (78%), especially Candida albicans (70%). Moreover, 24 eyes in 21 patients underwent vitrectomy, and 2 eyes underwent evisceration. Retinal detachment (RD) occurred in 17 eyes (35%) in 14 patients, and eyes without RD exhibited significantly superior visual outcomes (p = 0.001). A comparison of the initial VA between the better (20/200 or better) and worse groups (worse than 20/200) revealed that better initial VA was related to a superior visual outcome (p = 0.003). Therefore, to achieve superior visual outcomes, early diagnosis and prompt treatment are necessary for patients with EFE.