Results 21 to 30 of about 11,837 (217)

Tomografia de coerência óptica em pacientes com retinopatia da prematuridade [PDF]

open access: yes, 2007
PURPOSE: To describe morphological features of the macula in patients with retinopathy of prematurity. METHODS: Twelve premature babies with retinopathy of prematurity grades I, II and III underwent dilated fundus examination and optical coherence ...
Baba, Natalia Tamie   +6 more
core   +2 more sources

High resolution spectral domain optical coherence tomography (SD-OCT) in multiple sclerosis, Part II - the Total Macular Volume. The first follow up study over two years.

open access: yesFrontiers in Neurology, 2014
Background: To date, the results of studies investigating the use of optical coherence tomography (OCT) in multiple sclerosis (MS) patients seem to be preliminary, and at times contradictory.
Nermin eSerbecic   +7 more
doaj   +1 more source

Antioxidant vitamin and mineral supplements for slowing the progression of age-related macular degeneration. [PDF]

open access: yes, 2006
BACKGROUND: It has been proposed that antioxidants may prevent cellular damage in the retina by reacting with free radicals that are produced in the process of light absorption.
Bahrami   +51 more
core   +1 more source

Macular pigment optical density in a Brazilian sample

open access: yesInternational Journal of Retina and Vitreous, 2018
Background To evaluate macular pigment optical density (MPOD) and to identify its determinants in a sample of Brazilian individuals. Methods This was a cross-sectional study.
Letícia Pinto Coelho Jorge   +3 more
doaj   +1 more source

Good visual outcome in a longstanding macular detachment associated with an optic disc pit treated with vitrectomy, laser, and gas tamponade: case report.
doi: 10.20513/2447-6595.2016v56n1p68-70

open access: yesRevista de Medicina da UFC, 2016
Optic disc pit is a congenital anomaly of the optic nerve frequently associated with macula detachment. It has a poor visual prognosis if left untreated.
Ricardo Evangelista Marrocos de Aragao   +8 more
doaj   +1 more source

Perubahan Anatomi Bola Mata pada Penderita Diabetes Mellitus [PDF]

open access: yes, 2015
Diabetes Melitus (DM) adalah gangguan metabolisme, baik secara genetis maupun klinis, bermanifestasi dengan hilangnya tolerensi karbohidrat. Diabetes melitus ditandai dengan hiperglikemia puasa dan postprandial, aterosklerotik dan penyakit vaskular ...
Septadina, I. S. (Indri)
core   +2 more sources

Tratamento do buraco macular traumático: relato de caso [PDF]

open access: yes, 2008
Traumatic macular hole is a disease whose pathogenesis is not fully understood and the best treatment guideline is controversial. We report 2 cases of traumatic macular hole with different treatment approaches.
Brasil, Oswaldo Ferreira Moura   +1 more
core   +2 more sources

Comparison of ganglion cell-inner plexiform layer thickness among patients with intermittent exotropia according to fixation preference: a retrospective observational study [PDF]

open access: yesJournal of Yeungnam Medical Science
Background This study was performed to compare the thickness of the ganglion cell-inner plexiform layer (GCIPL) depending on the presence or absence of fixation preference in patients with intermittent exotropia (IXT) with refractive values close to ...
Yeon Ju Lim, Soo Jung Lee
doaj   +1 more source

Development of zeaxanthin‐rich tomato fruit through genetic manipulations of carotenoid biosynthesis

open access: yesPlant Biotechnology Journal, Volume 18, Issue 11, Page 2292-2303, November 2020., 2020
Summary The oxygenated carotenoid zeaxanthin provides numerous benefits to human health due to its antioxidant properties. Especially it is linked to protecting, together with the xanthophyll lutein, the retina in the human eye by filtering harmful blue light thus delaying the progression of age‐related macular degeneration (AMD), the most prevalent ...
Uri Karniel   +3 more
wiley   +1 more source

Sjögren‐Larsson syndrome: The mild end of the phenotypic spectrum

open access: yesJIMD Reports, Volume 53, Issue 1, Page 61-70, May 2020., 2020
Abstract Sjögren‐Larsson syndrome (SLS) is a rare inborn error of lipid metabolism. The syndrome is caused by mutations in the ALDH3A2 gene, resulting in a deficiency of fatty aldehyde dehydrogenase. Most patients have a clearly recognizable severe phenotype, with congenital ichthyosis, intellectual disability, and spastic diplegia.
Pippa Staps   +8 more
wiley   +1 more source

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