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Clinical Ophthalmology: A Systematic Approach
TLDR
Ocular side-effects of systemic medication 21.1.Abstract:
1. Eyelids 2. Lacrimal Drainage System 3. Orbit 4. Dry Eye Disorders 5. Conjunctiva 6. Cornea 7. Corneal and Refractive Surgery 8. Episclera and Sclera 9. Lens 10. Glaucoma 11. Uveitis 12. Ocular Tumours 13. Retinal Vascular Disease 14. Acquired Macular Disorders 15. Hereditary Fundus Dystrophies 16. Retinal Detachment 17. Vitreous Opacities 18. Strabismus 19. Neuro-ophthalmology 20. Ocular side-effects of systemic medication 21. Trauma Indexread more
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Journal ArticleDOI
Long term follow-up of a family with GUCY2D dominant cone dystrophy.
Georgios Tsokolas,Hussein Almuhtaseb,Helen Griffiths,Fatima Shawkat,Reuben J. Pengelly,Ennis Sarah,Andrew J. Lotery +6 more
TL;DR: Long term follow-up in a family with GUCY2D dominant cone dystrophy exhibited gradual changes in their fundi, electrophysiological testing and multimodal imaging, which were milder than those observed in other mutations of the same gene.
Journal ArticleDOI
Enhancement of blood vessels in retinal imaging using the nonsubsampled contourlet transform
TL;DR: The proposed method uses the NSCT to decompose the input retinal image into eight directions from coarser to finer scales, and then analyzes and classifies the image pixels into three categories: vessel, uncertainty, and non-vessel pixels, according to theNSCT coefficients.
Journal ArticleDOI
CT and MR imaging of contact lenses and intraocular lens implants.
TL;DR: Soft and rigid contact lenses can be seen in vitro in both methods but in vivo imaging was insensitive, and intraocular lens implants were detected in all CT, but were harder to detect by the MRI.
Journal ArticleDOI
Allergy and infections: long-term improvement of vernal keratoconjunctivitis following viral conjunctivitis.
TL;DR: The viral infection seemed to induce a clinical recovery of allergic disease, suggesting that an immune deviation induced by Th1-polarizing agents may revert an ongoing Th2 inflammation.
Journal ArticleDOI
Presence of the R1748X Mutation in the NF1 Gene in a Brazilian Patient with Ectropion uveae
TL;DR: A patient is described with ectropion and the mutation R1748X in the NF1 gene and the association is confirmed by other authors, which means that NF1 patients should be examined for the presence of ectropions and, consequently, for the development of glaucoma.