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Model of a Support Vector Machine to Assess the Functional Cure for Surgery of Intermittent Exotropia

Scientific reports, 2019-06, Vol.9 (1), p.8321-8321, Article 8321

2019

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A Meta-Analysis of Choroidal Thickness Changes in Unilateral Amblyopia

Journal of ophthalmology, 2017-01, Vol.2017 (2017), p.1-10

2017

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Autosomal-Dominant Retinitis Pigmentosa Caused by a Mutation in SNRNP200, a Gene Required for Unwinding of U4/U6 snRNAs

American journal of human genetics, 2009-11, Vol.85 (5), p.617-627

2009

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Timing-dependent LTP and LTD in mouse primary visual cortex following different visual deprivation models

PloS one, 2017-05, Vol.12 (5), p.e0176603-e0176603

2017

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Dark exposure extends the integration window for spike-timing-dependent plasticity

The Journal of neuroscience, 2012-10, Vol.32 (43), p.15027-15035

2012

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Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2

PloS one, 2014-05, Vol.9 (5), p.e97808-e97808

2014

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Targeted next-generation sequencing reveals novel USH2A mutations associated with diverse disease phenotypes: implications for clinical and molecular diagnosis

PloS one, 2014-08, Vol.9 (8), p.e105439-e105439

2014

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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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Superior oblique tucking for treatment of superior oblique palsy

Journal of pediatric ophthalmology and strabismus, 2014-07, Vol.51 (4), p.249-254

2014

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The ophthalmology surgical competency assessment rubric for strabismus surgery

Journal of AAPOS, 2012-08, Vol.16 (4), p.318-321

2012

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The influences of dark rearing on the transmission characteristics of layer II/III pyramidal cells during the critical period

Brain research, 2012-05, Vol.1457, p.26-32

2012

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Comparison of augmented and nonaugmented modified Knapp procedure for the treatment of nonrestrictive double-elevator palsies

Journal of AAPOS, 2016-10, Vol.20 (5), p.401-404

2016

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Differential dendritic shrinkage of α and β retinal ganglion cells in cats with chronic glaucoma

Investigative ophthalmology & visual science, 2003-07, Vol.44 (7), p.3005-3010

2003

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A Novel Homozygous BEST1 Mutation Correlates with Complex Ocular Phenotypes

Ophthalmology (Rochester, Minn.), 2013-07, Vol.120 (7), p.1511-1512.e2

2013

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Knocking Down Snrnp200 Initiates Demorphogenesis of Rod Photoreceptors in Zebrafish

Journal of ophthalmology, 2015-01, Vol.2015 (2015), p.1-7

2015

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A novel locus (RP33) for autosomal dominant retinitis pigmentosa mapping to chromosomal region 2cen-q12.1

Human genetics, 2006-07, Vol.119 (6), p.617-623

2006

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Comparison of surgical outcomes between bilateral recession and unilateral recession-resection in moderate-angle intermittent exotropia

Journal of AAPOS, 2019-04, Vol.23 (2), p.79.e1-79.e7

2019

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Strabismus fixus associated with congenital orbital fibrosis in children

Indian journal of ophthalmology, 2021-10, Vol.1 (4), p.768

2021

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Surgical management of large-angle incomitant strabismus in patients with oculomotor nerve palsy

Journal of AAPOS, 2008-02, Vol.12 (1), p.49-53

2008

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The aberration and the modulation transfer function in LASEK and LASIK: Pupil size dependence

Optik (Stuttgart), 2010-03, Vol.121 (6), p.500-505

2010

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Magnetic Resonance Imaging Findings in Patients With Duane Retraction Syndrome

Journal of neuro-ophthalmology, 2024-03, Vol.44 (1), p.101-106

2024

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PRPF4 mutations cause autosomal dominant retinitis pigmentosa

Human molecular genetics, 2014-06, Vol.23 (11), p.2926-2939

2014

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Strabismus fixus associated with congenital orbital fibrosis in children

Indian Journal of Ophthalmology - Case Reports, 2021-10, Vol.1 (4), p.768-770

2021

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Predicting Risk Factors for Consecutive Esotropia Failed with Conservative Therapy

Seminars in ophthalmology, 2021-02, Vol.36 (1-2), p.14-18

2021

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Model of a Support Vector Machine to Assess the Functional Cure for Surgery of Intermittent Exotropia

A Meta-Analysis of Choroidal Thickness Changes in Unilateral Amblyopia

Autosomal-Dominant Retinitis Pigmentosa Caused by a Mutation in SNRNP200, a Gene Required for Unwinding of U4/U6 snRNAs

Timing-dependent LTP and LTD in mouse primary visual cortex following different visual deprivation models

Dark exposure extends the integration window for spike-timing-dependent plasticity

Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2

Targeted next-generation sequencing reveals novel USH2A mutations associated with diverse disease phenotypes: implications for clinical and molecular diagnosis

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

Superior oblique tucking for treatment of superior oblique palsy

The ophthalmology surgical competency assessment rubric for strabismus surgery

The influences of dark rearing on the transmission characteristics of layer II/III pyramidal cells during the critical period

Comparison of augmented and nonaugmented modified Knapp procedure for the treatment of nonrestrictive double-elevator palsies

Differential dendritic shrinkage of α and β retinal ganglion cells in cats with chronic glaucoma

A Novel Homozygous BEST1 Mutation Correlates with Complex Ocular Phenotypes

Knocking Down Snrnp200 Initiates Demorphogenesis of Rod Photoreceptors in Zebrafish

A novel locus (RP33) for autosomal dominant retinitis pigmentosa mapping to chromosomal region 2cen-q12.1

Comparison of surgical outcomes between bilateral recession and unilateral recession-resection in moderate-angle intermittent exotropia

Strabismus fixus associated with congenital orbital fibrosis in children

Surgical management of large-angle incomitant strabismus in patients with oculomotor nerve palsy

The aberration and the modulation transfer function in LASEK and LASIK: Pupil size dependence

Magnetic Resonance Imaging Findings in Patients With Duane Retraction Syndrome

PRPF4 mutations cause autosomal dominant retinitis pigmentosa

Strabismus fixus associated with congenital orbital fibrosis in children

Predicting Risk Factors for Consecutive Esotropia Failed with Conservative Therapy

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