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Central serous chorioretinopathy: Towards an evidence-based treatment guideline

Progress in retinal and eye research, 2019-11, Vol.73, p.100770-100770, Article 100770

2019

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Discrepancy in current central serous chorioretinopathy classification

British journal of ophthalmology, 2019-06, Vol.103 (6), p.737

2019

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Whole Exome Sequencing Identifies CRB1 Defect in an Unusual Maculopathy Phenotype

Ophthalmology (Rochester, Minn.), 2014-09, Vol.121 (9), p.1773-1782

2014

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Mutations in the CEP290 ( NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis

American journal of human genetics, 2006-09, Vol.79 (3), p.556-561

2006

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Risk of Recurrence and Transition to Chronic Disease in Acute Central Serous Chorioretinopathy

Clinical ophthalmology (Auckland, N.Z.), 2020-01, Vol.14, p.1165-1175

2020

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GENETIC RISK FACTORS IN ACUTE CENTRAL SEROUS CHORIORETINOPATHY

Retina (Philadelphia, Pa.), 2019-12, Vol.39 (12), p.2303

2019

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Multimodal Imaging-Based Central Serous Chorioretinopathy Classification

Ophthalmology retina, 2020-11, Vol.4 (11), p.1043-1046

2020

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Editorial: Expanded insights into diabetic neovascular glaucoma by widefield swept-source optical coherence tomography angiography

Graefe's archive for clinical and experimental ophthalmology, 2024-04, Vol.262 (4), p.1015-1016

2024

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Three Cases of Erdheim-Chester Disease with Intraocular Manifestations: Imaging and Histopathology Findings of A Rare Entity

American journal of ophthalmology, 2017-04, Vol.176, p.141-147

2017

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New best1 mutations in autosomal recessive bestrophinopathy

Retina (Philadelphia, Pa.), 2015-04, Vol.35 (4), p.773

2015

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Perspectives and Update on the Global Shortage of Verteporfin (Visudyne®)

Ophthalmology and therapy, 2024-07, Vol.13 (7), p.1821-1831

2024

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High Levels of C-Reactive Protein with Low Levels of Pentraxin 3 as Biomarkers for Central Serous Chorioretinopathy

Ophthalmology science (Online), 2023-09, Vol.3 (3), p.100278-100278, Article 100278

2023

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Evaluation of Sleep Quality and Fatigue in Patients with Usher Syndrome Type 2a

Ophthalmology science (Online), 2023-12, Vol.3 (4), p.100323-100323, Article 100323

2023

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Abnormality in the external limiting membrane in early Stargardt Disease

Ophthalmic genetics, 2013-03, Vol.34 (1-2), p.75-77

2013

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Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosa

European journal of human genetics : EJHG, 2004-12, Vol.12 (12), p.1024-1032

2004

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LONG-TERM TREATMENT OUTCOMES AFTER BEVACIZUMAB THERAPY FOR MACULAR NEOVASCULARIZATION IN WHITE PATIENTS WITH HIGH MYOPIA

Retina (Philadelphia, Pa.), 2023-03, Vol.43 (3), p.444

2023

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Reticular pseudodrusen in early age-related macular degeneration are associated with choroidal thinning

Investigative ophthalmology & visual science, 2013-10, Vol.54 (10), p.7075-7081

2013

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Clinical and genetic misdiagnosis of autosomal recessive bestrophinopathy

JAMA ophthalmology, 2013-12, Vol.131 (12), p.1651

2013

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Long-term visual and anatomic outcomes of patients with peripapillary pachychoroid syndrome

British journal of ophthalmology, 2022-04, Vol.106 (4), p.576

2022

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Staphyloma-induced Serous Maculopathy

Ophthalmology retina, 2024-05, Vol.8 (5), p.499-508

2024

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Multimodal imaging comparison of perifoveal exudative vascular anomalous complex and resembling lesions

Acta ophthalmologica (Oxford, England), 2021-08, Vol.99 (5), p.553-558

2021

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Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants

Human genetics, 2022-11, Vol.141 (11), p.1723-1738

2022

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Incidence and Risk Factors of Second Eye Involvement in Myopic Macular Neovascularization

Ophthalmology retina, 2023-11, Vol.7 (11), p.1010-1016

2023

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Validation of central serous chorioretinopathy multimodal imaging-based classification system

Graefe's archive for clinical and experimental ophthalmology, 2022-04, Vol.260 (4), p.1161-1169

2022

Volltextzugriff (PDF)

Segmentation of Locally Varying Numbers of Outer Retinal Layers by a Model Selection Approach

IEEE transactions on medical imaging, 2017-06, Vol.36 (6), p.1306-1315

2017

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Central serous chorioretinopathy: Towards an evidence-based treatment guideline

Discrepancy in current central serous chorioretinopathy classification

Whole Exome Sequencing Identifies CRB1 Defect in an Unusual Maculopathy Phenotype

Mutations in the CEP290 ( NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis

Risk of Recurrence and Transition to Chronic Disease in Acute Central Serous Chorioretinopathy

GENETIC RISK FACTORS IN ACUTE CENTRAL SEROUS CHORIORETINOPATHY

Multimodal Imaging-Based Central Serous Chorioretinopathy Classification

Editorial: Expanded insights into diabetic neovascular glaucoma by widefield swept-source optical coherence tomography angiography

Three Cases of Erdheim-Chester Disease with Intraocular Manifestations: Imaging and Histopathology Findings of A Rare Entity

New best1 mutations in autosomal recessive bestrophinopathy

Perspectives and Update on the Global Shortage of Verteporfin (Visudyne®)

High Levels of C-Reactive Protein with Low Levels of Pentraxin 3 as Biomarkers for Central Serous Chorioretinopathy

Evaluation of Sleep Quality and Fatigue in Patients with Usher Syndrome Type 2a

Abnormality in the external limiting membrane in early Stargardt Disease

Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosa

LONG-TERM TREATMENT OUTCOMES AFTER BEVACIZUMAB THERAPY FOR MACULAR NEOVASCULARIZATION IN WHITE PATIENTS WITH HIGH MYOPIA

Reticular pseudodrusen in early age-related macular degeneration are associated with choroidal thinning

Clinical and genetic misdiagnosis of autosomal recessive bestrophinopathy

Long-term visual and anatomic outcomes of patients with peripapillary pachychoroid syndrome

Staphyloma-induced Serous Maculopathy

Multimodal imaging comparison of perifoveal exudative vascular anomalous complex and resembling lesions

Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants

Incidence and Risk Factors of Second Eye Involvement in Myopic Macular Neovascularization

Validation of central serous chorioretinopathy multimodal imaging-based classification system

Segmentation of Locally Varying Numbers of Outer Retinal Layers by a Model Selection Approach

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