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Title
Sickle cell retinopathy. A focused review
Authors
Keywords
Hemoglobin S, Hemoglobin C, Ischemia, Neovascularization, Panretinal photocoagulation, Sickle cell retinopathy
Journal
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
Volume -, Issue -, Pages -
Publisher
Springer Nature
Online
2019-03-20
DOI
10.1007/s00417-019-04294-2
References
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Related references
Note: Only part of the references are listed.- Paramacular temporal atrophy in sickle cell disease occurs early in childhood
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- Retinal Photocoagulation for Proliferative Sickle Cell Retinopathy: A Prospective Clinical Trial with New Sea Fan Classification
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- Clinical and Ophthalmic Factors Associated With the Severity of Sickle Cell Retinopathy
- (2018) Xiangyun J. Duan et al. AMERICAN JOURNAL OF OPHTHALMOLOGY
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- (2018) Umar K. Mian et al. BRITISH JOURNAL OF HAEMATOLOGY
- Gene Therapy Approaches to Hemoglobinopathies
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- Association between Sickle Cell Trait and the Prevalence and Severity of Diabetic Retinopathy
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- Increased circulating PEDF and low sICAM-1 are associated with sickle cell retinopathy
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- Measuring the precise area of peripheral retinal non-perfusion using ultra-widefield imaging and its correlation with the ischaemic index
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- Red cell exchange transfusion halts progressive proliferative sickle cell retinopathy in a teenaged patient with hemoglobin SC disease
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- Bevacizumab prior to vitrectomy for diabetic traction retinal detachment
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- Recurrent Infarction of Sphenoid Bone With Subperiosteal Collection in a Child With Sickle Cell Disease
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- Deferoxamine mesylate is toxic for retinal pigment epithelium cellsin vitro, and its toxicity is mediated by p38
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