Results 11 to 20 of about 25,913 (280)

Scleral inflammatory disease.

open access: greenAJNR. American journal of neuroradiology, 1987
Scleral inflammatory disease, a relatively common disease of the eye, is demonstrable on CT. Because of its unilateral and sometimes focal involvement, it may be mistaken for more serious diseases, both clinically and by CT. In particular, the clinical difficulties in diagnosing posterior scleritis have led to enucleations when such entities as ...
M H, Johnson   +3 more
openaire   +3 more sources

‘Pulsed’ immunosuppressive therapy in the treatment of immunologically induced corneal and scleral disease [PDF]

open access: bronzeEye, 1987
'Pulsed' immunosuppressive therapy, using methylprednisolone with or without cyclophosphamide, has effectively controlled severe destructive corneal and scleral disease that had been unresponsive to oral steroids. Thirty-seven patients have been treated in this manner and the results, complications and possible mechanism of action are discussed.
P A, Meyer   +3 more
openaire   +3 more sources

Scleral topography and its usefulness in scleral lens fitting

open access: yesAfrican Vision and Eye Health, 2021
Background: Scleral lenses are one of the best options to manage corneal irregularities and severe ocular surface diseases. As scleral lenses rest on the sclera, scleral topographical data are necessary when fitting these lenses.
Raymond G. Mabaso, Hlupheka L. Sithole
doaj   +1 more source

Management of ocular surface irregularity with scleral contact lenses: Experience from a tertiary eye care center

open access: yesKerala Journal of Ophthalmology, 2023
Purpose: This review focuses on the optical and therapeutic benefits which can be offered to patients by evaluating them for scleral contact lenses, and the purpose of this study is to select the indications and to find out how efficient the scleral ...
Aneeta Jabbar
doaj   +1 more source

The evolution of an active solitary idiopathic choroiditis (focal scleral nodule): a case report of the natural course and a review of the literature

open access: yesBMC Ophthalmology, 2021
Background To describe the clinical course of an active solitary idiopathic choroiditis (focal scleral nodule) that nearly resolved over six weeks without intervention.
Yilin Feng   +2 more
doaj   +1 more source

Shaping Eyeballs by Scleral Collagen Cross-Linking: A Hypothesis for Myopia Treatment

open access: yesFrontiers in Medicine, 2021
The global prevalence of myopia has brought to the attention of the different eye and vision specialists, who make way to control its progression. Evidence have shown that a proactive reshaping of the eyeball is the core point of myopia developing ...
Mengmeng Wang   +2 more
doaj   +1 more source

Vitreous function and intervention of it with vitrectomy and other modalities [PDF]

open access: yesInternational Journal of Ophthalmology, 2022
The vitreous body, the largest intraocular component, plays a key role in eye development, refraction, cell barrier function, oxygen metabolism and the pathogenesis of assorted diseases.
Yao Zong, Qian-Ying Gao, Yan-Nian Hui
doaj   +1 more source

[RETRACTED]Vitreous function and intervention of it with vitrectomy and other modalities [PDF]

open access: yesInternational Journal of Ophthalmology, 2021
[RETRACTED]The vitreous body, the largest intraocular component, plays a key role in eye development, refraction, cell barrier function, oxygen metabolism and the pathogenesis of assorted diseases. Age, refraction and systemic diseases can cause vitreous
Yao Zong, Qian-Ying Gao, Yan-Nian Hui
doaj   +1 more source

Clinical Features of Osteogenesis Imperfecta in Taiwan

open access: yesJournal of the Formosan Medical Association, 2009
Osteogenesis imperfecta (OI) (MIM 166200, 166210, 259420 and 166220) is a congenital disorder characterized by increased bone fragility and low bone mass. Information regarding the clinical features of this genetic disorder is lacking in Taiwan.
Hsiang-Yu Lin   +5 more
doaj   +1 more source

Genotype-phenotype correlation study in 364 osteogenesis imperfecta Italian patients [PDF]

open access: yes, 2019
Osteogenesis imperfecta (OI) is a rare genetic disorder of the connective tissue and 90% of cases are due to dominant mutations in COL1A1 and COL1A2 genes.
Boarini, Manila   +11 more
core   +1 more source

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