Meng X - Search Results

1

Varied clinical presentations of RP1L1 variants in Chinese patients: a study of occult macular dystrophy and vitelliform macular dystrophy.

Liu X, Long Y, Wang Y, Liu B, Ren J, Wang G, Wang M, Meng X, Liu Y. Liu X, et al. Among authors: meng x. BMC Ophthalmol. 2024 Aug 6;24(1):327. doi: 10.1186/s12886-024-03591-7. BMC Ophthalmol. 2024. PMID: 39107704 Free PMC article.

2

The characterization of functional disturbances in Chinese patients with Bietti's crystalline dystrophy at different fundus stages.

Liu DN, Liu Y, Meng XH, Yin ZQ. Liu DN, et al. Graefes Arch Clin Exp Ophthalmol. 2012 Feb;250(2):191-200. doi: 10.1007/s00417-011-1809-3. Epub 2011 Sep 3. Graefes Arch Clin Exp Ophthalmol. 2012. PMID: 21892605

3

Transient pupillary light reflex in relation to fundus autofluorescence and dark-adapted perimetry in typical retinitis pigmentosa.

Liu Y, Liu DN, Meng XH, Yin ZQ. Liu Y, et al. Ophthalmic Res. 2012;47(3):113-21. doi: 10.1159/000330049. Epub 2011 Oct 11. Ophthalmic Res. 2012. PMID: 21997281

4

[Contributions of human rods and cones pathway to different components of oscillatory potentials in time and frequency domain].

Dai J, Li S, Yin Z, Wang G, Meng X. Dai J, et al. Among authors: meng x. Zhonghua Yan Ke Za Zhi. 2015 May;51(5):369-73. Zhonghua Yan Ke Za Zhi. 2015. PMID: 26311699 Chinese.

5

PRPF3-Associated Autosomal Dominant Retinitis Pigmentosa and CYP4V2-Associated Bietti's Crystalline Corneoretinal Dystrophy Coexist in a Multigenerational Chinese Family.

Meng X, Li Q, Guo H, Xu H, Li S, Yin Z. Meng X, et al. J Ophthalmol. 2017;2017:4156386. doi: 10.1155/2017/4156386. Epub 2017 Aug 7. J Ophthalmol. 2017. PMID: 28848678 Free PMC article.

6

Long-term safety of human retinal progenitor cell transplantation in retinitis pigmentosa patients.

Liu Y, Chen SJ, Li SY, Qu LH, Meng XH, Wang Y, Xu HW, Liang ZQ, Yin ZQ. Liu Y, et al. Stem Cell Res Ther. 2017 Sep 29;8(1):209. doi: 10.1186/s13287-017-0661-8. Stem Cell Res Ther. 2017. PMID: 28962643 Free PMC article. Clinical Trial.

7

Novel mutations in CYP4V2 in Bietti corneoretinal crystalline dystrophy: Next-generation sequencing technology and genotype-phenotype correlations.

Meng XH, He Y, Zhao TT, Li SY, Liu Y, Yin ZQ. Meng XH, et al. Mol Vis. 2019 Oct 31;25:654-662. eCollection 2019. Mol Vis. 2019. PMID: 31741654 Free PMC article.

8

Identification of 13 novel USH2A mutations in Chinese retinitis pigmentosa and Usher syndrome patients by targeted next-generation sequencing.

Qu LH, Jin X, Long YL, Ren JY, Weng CH, Xu HW, Liu Y, Meng XH, Li SY, Yin ZQ. Qu LH, et al. Among authors: meng xh. Biosci Rep. 2020 Jan 31;40(1):BSR20193536. doi: 10.1042/BSR20193536. Biosci Rep. 2020. PMID: 31904091 Free PMC article.

9

Electrophysiological and Structural Changes in Chinese Patients with LHON.

Wang M, Guo H, Li S, Wang G, Long Y, Meng X, Liu B, Liu Y, Robson AG, Yin ZQ. Wang M, et al. Among authors: meng x. J Ophthalmol. 2020 Mar 30;2020:4734276. doi: 10.1155/2020/4734276. eCollection 2020. J Ophthalmol. 2020. PMID: 32318281 Free PMC article.

10

Oguchi disease caused by a homozygous novel SAG splicing alteration associated with the multiple evanescent white dot syndrome: A 15-month follow-up.

Liu X, Gao L, Wang G, Long Y, Ren J, Fujinami K, Meng X, Li S. Liu X, et al. Among authors: meng x. Doc Ophthalmol. 2020 Dec;141(3):217-226. doi: 10.1007/s10633-020-09766-z. Epub 2020 Apr 24. Doc Ophthalmol. 2020. PMID: 32333190

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