Han G - Search Results

1

Cobalamin C Deficiency Shows a Rapidly Progressing Maculopathy With Severe Photoreceptor and Ganglion Cell Loss.

Bonafede L, Ficicioglu CH, Serrano L, Han G, Morgan JI, Mills MD, Forbes BJ, Davidson SL, Binenbaum G, Kaplan PB, Nichols CW, Verloo P, Leroy BP, Maguire AM, Aleman TS. Bonafede L, et al. Among authors: han g. Invest Ophthalmol Vis Sci. 2015 Dec;56(13):7875-87. doi: 10.1167/iovs.15-17857. Invest Ophthalmol Vis Sci. 2015. PMID: 26658511 Free PMC article.

2

High-resolution adaptive optics retinal imaging of cellular structure in choroideremia.

Morgan JI, Han G, Klinman E, Maguire WM, Chung DC, Maguire AM, Bennett J. Morgan JI, et al. Among authors: han g. Invest Ophthalmol Vis Sci. 2014 Sep 4;55(10):6381-97. doi: 10.1167/iovs.13-13454. Invest Ophthalmol Vis Sci. 2014. PMID: 25190651 Free PMC article. Clinical Trial.

3

Detailed functional and structural phenotype of Bietti crystalline dystrophy associated with mutations in CYP4V2 complicated by choroidal neovascularization.

Fuerst NM, Serrano L, Han G, Morgan JI, Maguire AM, Leroy BP, Kim BJ, Aleman TS. Fuerst NM, et al. Among authors: han g. Ophthalmic Genet. 2016 Dec;37(4):445-452. doi: 10.3109/13816810.2015.1126616. Epub 2016 Mar 30. Ophthalmic Genet. 2016. PMID: 27028354 Free PMC article.

4

Natural History of the Central Structural Abnormalities in Choroideremia: A Prospective Cross-Sectional Study.

Aleman TS, Han G, Serrano LW, Fuerst NM, Charlson ES, Pearson DJ, Chung DC, Traband A, Pan W, Ying GS, Bennett J, Maguire AM, Morgan JI. Aleman TS, et al. Among authors: han g. Ophthalmology. 2017 Mar;124(3):359-373. doi: 10.1016/j.ophtha.2016.10.022. Epub 2016 Dec 13. Ophthalmology. 2017. PMID: 27986385 Free PMC article.

5

Structural and Electrophysiologic Outcomes in a Patient with Retinal Metallosis.

Sulewski ME Jr, Serrano LW, Han G, Aleman TS, Nichols CW. Sulewski ME Jr, et al. Among authors: han g. Ophthalmol Retina. 2018 Feb;2(2):173-175. doi: 10.1016/j.oret.2017.07.014. Epub 2017 Sep 28. Ophthalmol Retina. 2018. PMID: 29756079 Free PMC article. No abstract available.

6

Detailed retinal phenotype of Boucher-Neuhäuser syndrome associated with mutations in PNPLA6 mimicking choroideremia.

O'Neil E, Serrano L, Scoles D, Cunningham KE, Han G, Chiang J, Bennett J, Aleman TS. O'Neil E, et al. Among authors: han g. Ophthalmic Genet. 2019 Jun;40(3):267-275. doi: 10.1080/13816810.2019.1605392. Epub 2019 May 28. Ophthalmic Genet. 2019. PMID: 31135245

7

On variants and disease-causing mutations: Case studies of a SEMA4A variant identified in inherited blindness.

Bryant L, Lozynska O, Han G, Morgan JIW, Gai X, Maguire AM, Aleman T, Bennett J. Bryant L, et al. Among authors: han g. Ophthalmic Genet. 2018 Jan-Feb;39(1):144-146. doi: 10.1080/13816810.2017.1354384. Epub 2017 Aug 14. Ophthalmic Genet. 2018. PMID: 28805479 Free PMC article.

8

Multi-modal automatic montaging of adaptive optics retinal images.

Chen M, Cooper RF, Han GK, Gee J, Brainard DH, Morgan JI. Chen M, et al. Biomed Opt Express. 2016 Nov 3;7(12):4899-4918. doi: 10.1364/BOE.7.004899. eCollection 2016 Dec 1. Biomed Opt Express. 2016. PMID: 28018714 Free PMC article.

9

COVID-19 infection with severe hypocalcaemia and superior mesenteric artery syndrome-a case report.

Selva Raj SR, Han GH, Karupiah M, Nagendram SV, Kang WH. Selva Raj SR, et al. Among authors: han gh. AME Case Rep. 2024 Mar 22;8:54. doi: 10.21037/acr-23-106. eCollection 2024. AME Case Rep. 2024. PMID: 38711895 Free PMC article.

10

China Initiative for Multi-Domain Intervention (CHINA-IN-MUDI) to Prevent Cognitive Decline: Study Design and Progress.

Li SY, Xie XY, Liu D, Cheng GR, Hu FF, Zeng DY, Chen XC, Jia LF, Wang YJ, Bu XL, Qiu C, Gao F, Gu JG, Liu MF, Li Y, Zhou YL, Chang HJ, Ou YM, Xu L, Wu ZX, Zhang JJ, Wang JY, Huang LY, Cui YY, Zhou J, Liu XC, Liu J, Nie QQ, Song D, Cai C, Han GB, Yang X, Tan W, Yu JT, Zeng Y. Li SY, et al. Among authors: han gb. J Prev Alzheimers Dis. 2024;11(3):589-600. doi: 10.14283/jpad.2024.63. J Prev Alzheimers Dis. 2024. PMID: 38706275 Clinical Trial.

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