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Marc D. de Smet

Researcher at Leiden University

Publications -  153
Citations -  5252

Marc D. de Smet is an academic researcher from Leiden University. The author has contributed to research in topics: Uveitis & Medicine. The author has an hindex of 32, co-authored 138 publications receiving 4361 citations. Previous affiliations of Marc D. de Smet include Katholieke Universiteit Leuven & National Institutes of Health.

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The International Vitreomacular Traction Study Group classification of vitreomacular adhesion, traction, and macular hole.

TL;DR: This classification system will support systematic diagnosis and management by creating a clinically applicable system that is predictive of therapeutic outcomes and is useful for the execution and analysis of clinical studies.
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Recent developments in optical coherence tomography for imaging the retina.

TL;DR: An overview of the most recent developments in the field of OCT imaging focussing on applications for the retina shows how promising are the developments in contrast-enhanced molecular optical imaging, for example with the use of scattering tuneable nanoparticles targeted at specific tissue or cell structures.
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Understanding uveitis: The impact of research on visual outcomes

TL;DR: The aims of this review are to summarize the state of clinical research in uveitis, to identify gaps in knowledge, and to propose new opportunities and methodologies for future developments in all aspects of Uveitis research, including epidemiology, economic impact analysis, diagnosis, therapeutics, and clinical study design.
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The angio-fibrotic switch of VEGF and CTGF in proliferative diabetic retinopathy.

TL;DR: CTGF is primarily a pro-fibrotic factor in the eye, and a shift in the balance between CTGF and VEGF is associated with the switch from angiogenesis to fibrosis in proliferative retinopathy.
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Cellular immune responses of patients with uveitis to retinal antigens and their fragments.

TL;DR: Several patients were capable of responding to more than one epitope of the same antigen, which indicates that there are major differences between the experimental model and human autoimmune diseases in the response to autoantigens.