Suchergebnisse - "Ding, Xiaoyan"

PubPharm (9)

1

Genotype-Phenotype of CRB1-Associated Early-Onset Retinal Dystrophy : Novel Insights on Retinal Architecture and Therapeutic Window for Clinical Trials

enthalten in: Investigative ophthalmology & visual science | 2024

von Jin, Y. | Li, S. | Jiang, Z. | +5

2

HIGH MYOPIA IS COMMON IN PATIENTS WITH X-LINKED RETINOPATHIES : Myopic Maculopathy Analysis

enthalten in: Retina (Philadelphia, Pa.) | 2024

von Huang, L. | Lai, Y. | Sun, L. | +2

3

NDP-related retinopathies : clinical phenotype of female carriers

enthalten in: The British journal of ophthalmology | 2023

von Huang, L. | Sun, L. | Li, X. | +4

4

Ocular manifestations of Chinese patients with copy number variants in the NDP gene

enthalten in: Molecular vision | 2022

von Huang, L. | Zhang, L. | Li, X. | +5

5

Clinical manifestation and genetic analysis in Chinese early onset X-linked retinoschisis

enthalten in: Molecular genetics & genomic medicine | 2020

von Huang, L. | Sun, L. | Wang, Z. | +5

6

The spectrum of genetic mutations in patients with asymptomatic mild familial exudative vitreoretinopathy

enthalten in: Experimental eye research | 2020

von Chen, C. | Sun, L. | Li, S. | +5

7

Symmetry of folds in FEVR : A genotype-phenotype correlation study

enthalten in: Experimental eye research | 2019

von Wang, Z. | Chen, C. | Sun, L. | +4

8

Wnt5a Contributes to the Differentiation of Human Embryonic Stem Cells into Lentoid Bodies Through the Noncanonical Wnt/JNK Signaling Pathway

enthalten in: Investigative ophthalmology & visual science | 2018

von Han, C. | Li, J. | Wang, C. | +5

9

Mutation Spectrum of the LRP5, NDP, and TSPAN12 Genes in Chinese Patients With Familial Exudative Vitreoretinopathy

enthalten in: Investigative ophthalmology & visual science | 2017

von Tang, M. | Sun, L. | Hu, A. | +4

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