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Differences of ocular oscillations and neuro-retinal structures in patients with nystagmus caused by GPR143 and FRMD7 gene variants

Indian journal of ophthalmology, 2024-05, Vol.72 (Suppl 3), p.S509-S513

2024

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Augmented lateral rectus muscle recession for treatment of infantile exotropia

International ophthalmology, 2022-05, Vol.42 (5), p.1589-1594

2022

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Clinical and genetic characteristics of Chinese patients with congenital fibrosis of the extraocular muscles

Orphanet journal of rare diseases, 2024-08, Vol.19 (1), p.300-14

2024

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Thicknesses of the retina and choroid in children with retinitis pigmentosa

BMC ophthalmology, 2023-01, Vol.23 (1), p.25-25, Article 25

2023

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Clinical and genetic studies for a cohort of patients with congenital stationary night blindness

Orphanet journal of rare diseases, 2024-03, Vol.19 (1), p.101-101, Article 101

2024

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Case report: Exotropia in waardenburg syndrome with novel variations

Frontiers in genetics, 2022-09, Vol.13

2022

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Correlations of FRMD7 gene mutations with ocular oscillations

Scientific reports, 2022-06, Vol.12 (1), p.9914-9914, Article 9914

2022

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Analyses of eye movement parameters in children with anisometropic amblyopia

BMC ophthalmology, 2024-07, Vol.24 (1), p.278-9, Article 278

2024

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A randomized trial evaluating efficacy of overminus lenses combined with prism in the children with intermittent exotropia

BMC ophthalmology, 2021-02, Vol.21 (1), p.73-73, Article 73

2021

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Novel variants and phenotypes of ROBO3 gene associated with horizontal gaze palsy with progressive scoliosis

Pediatric investigation, 2024-03, Vol.8 (1), p.72-74

2024

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Local structural-functional connectivity decoupling of caudate nucleus in infantile esotropia

Frontiers in neuroscience, 2022-12, Vol.16, p.1098735-1098735

2022

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Analytical Design of Dual-Band Negative Group Delay Circuit With Multi-Coupled Lines

IEEE access, 2020, Vol.8, p.72749-72756

2020

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Diversity of clinical phenotypes in a cohort of Han Chinese patients with PAX6 variants

Frontiers in genetics, 2023-02, Vol.14, p.1011060-1011060

2023

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Abnormal developmental trends of functional connectivity in young children with infantile esotropia

Frontiers in neuroscience, 2022-08, Vol.16, p.972882-972882

2022

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S-Parameter Model of Three Parallel Interconnect Lines Generating Negative Group-Delay Effect

IEEE access, 2018, Vol.6, p.57152-57159

2018

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The Design Method of the Active Negative Group Delay Circuits Based on a Microwave Amplifier and an RL-Series Network

IEEE access, 2018-01, Vol.6, p.33849-33858

2018

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Alterations of large‐scale functional network connectivity in patients with infantile esotropia before and after surgery

Brain and behavior, 2023-08, Vol.13 (8), p.e3154-n/a

2023

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A modified Fox pentagon technique performed using a polytetrafluoroethylene sling in frontalis suspension to treat blepharophimosis syndrome

Science progress (1916), 2020-01, Vol.103 (1), p.1-9

2020

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Design, Modeling and Synthesis of Negative Group Delay IL-Shape Topology

IEEE access, 2019, Vol.7, p.153900-153909

2019

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A novel pathogenic variant of CEP164 in an infant with Senior‐Loken syndrome

Pediatric investigation, 2023-06, Vol.7 (2), p.140-143

2023

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Plasminogen activator inhibitor-1 4G/5G polymorphism and retinopathy risk in type 2 diabetes: a meta-analysis

BMC medicine, 2013-01, Vol.11 (1), p.1-1, Article 1

2013

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Association of OPA1 polymorphisms with NTG and HTG: a meta-analysis

PloS one, 2012-08, Vol.7 (8), p.e42387-e42387

2012

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Clinical features and genotypes of six patients from four families with horizontal gaze palsy with progressive scoliosis

Frontiers in pediatrics, 2022-09, Vol.10, p.949565-949565

2022

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Bilateral lateral rectus muscle recession for the convergence insufficiency type of intermittent exotropia

Journal of AAPOS, 2016-06, Vol.20 (3), p.194-196.e1

2016

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Time-Domain Experimentation of NGD ActiveRC-Network Cell

IEEE transactions on circuits and systems. II, Express briefs, 2019-04, Vol.66 (4), p.562-566

2019

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Differences of ocular oscillations and neuro-retinal structures in patients with nystagmus caused by GPR143 and FRMD7 gene variants

Augmented lateral rectus muscle recession for treatment of infantile exotropia

Clinical and genetic characteristics of Chinese patients with congenital fibrosis of the extraocular muscles

Thicknesses of the retina and choroid in children with retinitis pigmentosa

Clinical and genetic studies for a cohort of patients with congenital stationary night blindness

Case report: Exotropia in waardenburg syndrome with novel variations

Correlations of FRMD7 gene mutations with ocular oscillations

Analyses of eye movement parameters in children with anisometropic amblyopia

A randomized trial evaluating efficacy of overminus lenses combined with prism in the children with intermittent exotropia

Novel variants and phenotypes of ROBO3 gene associated with horizontal gaze palsy with progressive scoliosis

Local structural-functional connectivity decoupling of caudate nucleus in infantile esotropia

Analytical Design of Dual-Band Negative Group Delay Circuit With Multi-Coupled Lines

Diversity of clinical phenotypes in a cohort of Han Chinese patients with PAX6 variants

Abnormal developmental trends of functional connectivity in young children with infantile esotropia

S-Parameter Model of Three Parallel Interconnect Lines Generating Negative Group-Delay Effect

The Design Method of the Active Negative Group Delay Circuits Based on a Microwave Amplifier and an RL-Series Network

Alterations of large‐scale functional network connectivity in patients with infantile esotropia before and after surgery

A modified Fox pentagon technique performed using a polytetrafluoroethylene sling in frontalis suspension to treat blepharophimosis syndrome

Design, Modeling and Synthesis of Negative Group Delay IL-Shape Topology

A novel pathogenic variant of CEP164 in an infant with Senior‐Loken syndrome

Plasminogen activator inhibitor-1 4G/5G polymorphism and retinopathy risk in type 2 diabetes: a meta-analysis

Association of OPA1 polymorphisms with NTG and HTG: a meta-analysis

Clinical features and genotypes of six patients from four families with horizontal gaze palsy with progressive scoliosis

Bilateral lateral rectus muscle recession for the convergence insufficiency type of intermittent exotropia

Time-Domain Experimentation of NGD ActiveRC-Network Cell

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