نتایج جستجو برای: vitreoretinal degeneration

تعداد نتایج: 63315  

2017
Quraish Ghadiali Sarwar Zahid Rosa Dolz-Marco Anna Tan Michael Engelbert

Purpose. To compare the stages of vitreous degeneration in patients with vitreomacular traction (VMT) and macular holes (MH). Methods. A retrospective study was performed analyzing stages of vitreous degeneration of eyes with VMT or MH using swept-source optical coherence tomography (SS-OCT) and spectral-domain optical coherence tomography (SD-OCT). An analogous review was performed on a contro...

2003
S. MINDSZENTI

Two hereditary syndromes characterized by the association of retinal changes and erythrocytic anomalies have been described: (1) Retinopathy complicating haemoglobin anomalies, thalassaemia (Rudd, Evans, and Peeney, 1953), or sickle-cell anaemia (Lieb, Geeraets, and Guerry, 1959); (2) Atypical retinitis pigmentosa with thorny erythrocytes (acanthocytosis: Bassen and Kornzweig, 1950; Kornzweig a...

Journal: :The British journal of ophthalmology 1963
A KAHAN I L KAHAN A BENKO

Two hereditary syndromes characterized by the association of retinal changes and erythrocytic anomalies have been described: (1) Retinopathy complicating haemoglobin anomalies, thalassaemia (Rudd, Evans, and Peeney, 1953), or sickle-cell anaemia (Lieb, Geeraets, and Guerry, 1959); (2) Atypical retinitis pigmentosa with thorny erythrocytes (acanthocytosis: Bassen and Kornzweig, 1950; Kornzweig a...

2011
Carmen Sílvia Bongiovanni Carla Cristina Serra Ferreira Ana Paula Silvério Rodrigues João Borges Fortes Filho Márcia Beatriz Tartarella

Knobloch syndrome is an autosomal recessive disorder associated with early-onset ocular abnormalities and central nervous system malformations. Ocular abnormalities are usually severe, and include high myopia, vitreoretinal degeneration, retinal detachment, macular abnormalities, and cataract. The most frequent systemic changes are midline malformations of the brain, ventricular dilation, and o...

Journal: :Progress in retinal and eye research 2010
Wolfgang Berger Barbara Kloeckener-Gruissem John Neidhardt

During the last two to three decades, a large body of work has revealed the molecular basis of many human disorders, including retinal and vitreoretinal degenerations and dysfunctions. Although belonging to the group of orphan diseases, they affect probably more than two million people worldwide. Most excitingly, treatment of a particular form of congenital retinal degeneration is now possible....

2011
Eric W Schneider Mark W Johnson

With the dissemination of optical coherence tomography over the past two decades, the role of persistent vitreomacular adhesion (VMA) in the development of numerous macular pathologies - including idiopathic macular hole, vitreomacular traction syndrome, cystoid and diabetic macular edema, neovascularization in diabetic retinopathy and retinal vein occlusion, exudative age-related macular degen...

صعودی, رضا, مدرس زاده, سید مهدی , ملکی, آرش, میرزاجانی, حورا, نظری, حسین,

  Introduction : The vitreoretinal interface is involved in a wide range of vitreoretinal disorders and separation of the posterior vitreous face from the retinal surface is an essential part of vitrectomy surgeries. A diverse range of enzymatic and non-enzymatic agents are being studied as an adjunct before or during vitrectomy to facilitate the induction of posterior vitreous detachment. Ther...

Journal: :American journal of ophthalmology 1972
T M Aaberg T R Stevens

In 1904 and again in 1934, Gonin· de­ scribed the clinical characteristics of snail track degeneration of the retina. Sharply de­ marcated bands of white, crinkled, or frost­ like change of the inner retinal surface (Figs. 1 and 2) create a picture that is remi­ niscent of the tracks made by a snail; this appearance led to the descriptive naming of this entity. Several authors have commented on...

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