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Accuracy of automated machine learning in classifying retinal pathologies from ultra-widefield pseudocolour fundus images

British journal of ophthalmology, 2023-01, Vol.107 (1), p.90-95

2023

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Propagation and Selectivity of Axonal Loss in Leber Hereditary Optic Neuropathy

Scientific reports, 2019-04, Vol.9 (1), p.6720, Article 6720

2019

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Predictive modeling of proliferative vitreoretinopathy using automated machine learning by ophthalmologists without coding experience

Scientific reports, 2020-11, Vol.10 (1), p.19528-19528, Article 19528

2020

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Gene therapy for RPE65-related retinal disease

Ophthalmic genetics, 2018-11, Vol.39 (6), p.671-677

2018

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The prognostic value of peripheral retinal nonperfusion in diabetic retinopathy using ultra-widefield fluorescein angiography

Graefe's archive for clinical and experimental ophthalmology, 2020-12, Vol.258 (12), p.2681-2690

2020

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Author Correction: Propagation and Selectivity of Axonal Loss in Leber Hereditary Optic Neuropathy

Scientific reports, 2020-03, Vol.10 (1), p.4646-4646, Article 4646

2020

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Paracentral acute middle maculopathy in non-ischaemic central retinal vein occlusion: the role of en face optical coherence tomography

BMJ case reports, 2021-11, Vol.14 (11), p.e246842

2021

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Genotype and Phenotype Studies in Autosomal Dominant Retinitis Pigmentosa (adRP) of the French Canadian Founder Population

Investigative ophthalmology & visual science, 2015-12, Vol.56 (13), p.8297-8305

2015

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Genetic Diagnosis for 64 Patients with Inherited Retinal Disease

Genes, 2022-12, Vol.14 (1), p.74

2022

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Xp11.3 microdeletion causing Norrie disease and X-linked Kabuki syndrome

American journal of ophthalmology case reports, 2023-03, Vol.29, p.101798, Article 101798

2023

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Surgical management of lens subluxation in Marfan syndrome

Journal of AAPOS, 2014-04, Vol.18 (2), p.140-146

2014

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Treatment of cystic cavities in X-linked juvenile retinoschisis: The first sequential cross-over treatment regimen with dorzolamide

American journal of ophthalmology case reports, 2017-12, Vol.8 (C), p.1-3

2017

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Prognostic factors of postoperative intraretinal cystoid spaces after primary pars plana vitrectomy for vitreomacular traction

Journal of current ophthalmology, 2019-12, Vol.31 (4), p.399-405

2019

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Choroideremia: Effect of age on visual acuity in patients and female carriers

Ophthalmic genetics, 2012-06, Vol.33 (2), p.66-73

2012

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HLA-A29 negative Birdshot-like chorioretinopathy associated with common variable immunodeficiency

American journal of ophthalmology case reports, 2018-06, Vol.10, p.18-24

2018

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Simultaneous central retinal artery occlusion and optic nerve vasculitis in Crohn disease

American journal of ophthalmology case reports, 2017-04, Vol.5 (C), p.11-15

2017

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Anterior infectious necrotizing scleritis secondary to Pseudomonas aeruginosa infection following intravitreal ranibizumab injection

American journal of ophthalmology case reports, 2017-04, Vol.5 (C), p.16-19

2017

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Mitochondrial DNA A3243G variant-associated retinopathy: Current perspectives and clinical implications

Survey of ophthalmology, 2021-09, Vol.66 (5), p.838-855

2021

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Profiling of visual acuity and genotype correlations in RP2 patients: a cross-sectional comparative meta-analysis between carrier females and affected males

Eye (London), 2023-02, Vol.37 (2), p.350-355

2023

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Stickler syndrome: exploring prophylaxis for retinal detachment

Current opinion in ophthalmology, 2019-09, Vol.30 (5), p.306-313

2019

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Sector retinitis pigmentosa: Report of ten cases and a review of the literature

Molecular vision, 2019, Vol.25, p.869-889

2019

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Choroideremia: A review of general findings and pathogenesis

Ophthalmic genetics, 2012-06, Vol.33 (2), p.57-65

2012

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Novel mutation in CTNNB1 causes familial exudative vitreoretinopathy (FEVR) and microcephaly: case report and review of the literature

Ophthalmic genetics, 2020-01, Vol.41 (1), p.63-68

2020

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Blink detection and magnetic force generation for correction of lagophthalmos, with specific regard to implant compatibility testing

Orbit (Amsterdam), 2022-01, Vol.41 (1), p.59-68

2022

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Genotype and Phenotype Studies in Autosomal Dominant Retinitis Pigmentosa (adRP) of the French Canadian Founder Population

Investigative ophthalmology & visual science, 2015-12, Vol.56 (13), p.8297-8305

2015

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Accuracy of automated machine learning in classifying retinal pathologies from ultra-widefield pseudocolour fundus images

Propagation and Selectivity of Axonal Loss in Leber Hereditary Optic Neuropathy

Predictive modeling of proliferative vitreoretinopathy using automated machine learning by ophthalmologists without coding experience

Gene therapy for RPE65-related retinal disease

The prognostic value of peripheral retinal nonperfusion in diabetic retinopathy using ultra-widefield fluorescein angiography

Author Correction: Propagation and Selectivity of Axonal Loss in Leber Hereditary Optic Neuropathy

Paracentral acute middle maculopathy in non-ischaemic central retinal vein occlusion: the role of en face optical coherence tomography

Genotype and Phenotype Studies in Autosomal Dominant Retinitis Pigmentosa (adRP) of the French Canadian Founder Population

Genetic Diagnosis for 64 Patients with Inherited Retinal Disease

Xp11.3 microdeletion causing Norrie disease and X-linked Kabuki syndrome

Surgical management of lens subluxation in Marfan syndrome

Treatment of cystic cavities in X-linked juvenile retinoschisis: The first sequential cross-over treatment regimen with dorzolamide

Prognostic factors of postoperative intraretinal cystoid spaces after primary pars plana vitrectomy for vitreomacular traction

Choroideremia: Effect of age on visual acuity in patients and female carriers

HLA-A29 negative Birdshot-like chorioretinopathy associated with common variable immunodeficiency

Simultaneous central retinal artery occlusion and optic nerve vasculitis in Crohn disease

Anterior infectious necrotizing scleritis secondary to Pseudomonas aeruginosa infection following intravitreal ranibizumab injection

Mitochondrial DNA A3243G variant-associated retinopathy: Current perspectives and clinical implications

Profiling of visual acuity and genotype correlations in RP2 patients: a cross-sectional comparative meta-analysis between carrier females and affected males

Stickler syndrome: exploring prophylaxis for retinal detachment

Sector retinitis pigmentosa: Report of ten cases and a review of the literature

Choroideremia: A review of general findings and pathogenesis

Novel mutation in CTNNB1 causes familial exudative vitreoretinopathy (FEVR) and microcephaly: case report and review of the literature

Blink detection and magnetic force generation for correction of lagophthalmos, with specific regard to implant compatibility testing

Genotype and Phenotype Studies in Autosomal Dominant Retinitis Pigmentosa (adRP) of the French Canadian Founder Population

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