Search for dissertations about: "Lund Oftalmologi"
Showing result 1 - 5 of 54 swedish dissertations containing the words Lund Oftalmologi.
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1. Studies into The Mechanisms of Neurodegeneration and Neuroprotection in Rd1 Mouse Retina
Abstract : Retinitis Pigmentosa (RP) is a group of uncured retinal diseases with the world wide incidence of about 1/3500. In spite of the huge efforts in past years, the mechanisms underlying this type of hereditary blindness has not been elucidated and nor any effective treatment available. READ MORE
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2. Intracellular mechanisms in rd1 mouse retinal degeneration
Abstract : Retinitis pigmentosa (RP) is an inherited disorder and the leading cause of visual impairment in the working age population. It is caused by a number of different genetic mutations, all of which cause the rod photoreceptors to degenerate. As the rods become few in numbers, the cones will also begin to die, resulting in total blindness. READ MORE
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3. On visual impairment in Swedish children
Abstract : Knowledge of the epidemiology of visual impairment in children forms one of the cornerstones in paediatric ophthalmology. To gain an overview of the situation in Sweden an epidemiological study was performed. Totally 2373 visually impaired children were found, giving an age-specific prevalence of 10,9/10 000. Childhood blindness (i. READ MORE
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4. Diabetic retinopathy in type 1 diabetes mellitus. A study on medical risk indicators and treatment outcome
Abstract : Diabetic retinopathy is a common complication to diabetes mellitus and is still a major cause of impaired vision in the Western world. The aim of the present study was to identify medical risk factors influencing the development and progression of retinopathy in type 1 diabetic patients, and to investigate the effects of laser treatment on visual acuity and glare. READ MORE
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5. Phenotypes and genotypes in families with hereditary tapetoretinal degenerations
Abstract : The purpose of the study was to characterise the phenotype with emphasis on electroretinography in four different types of hereditary retinal degeneration and to correlate it to a genotype when possible. Two methods were used: full-field electroretinography for objective assessment of retinal function and mutation screening of blood samples for detection of gene alterations. READ MORE
