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Survey of Ophthalmology, 1988
Retinitis pigmentosa is a clinically and genetically heterogeneous group of hereditary disorders in which there is progressive loss of photoreceptor and pigment epithelial function. The prevalence of retinitis pigmentosa is between 1/3000 and 1/5000 making it one of the most common causes of visual impairment in all age groups.
Roberta A Pagon
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Retinitis pigmentosa is a clinically and genetically heterogeneous group of hereditary disorders in which there is progressive loss of photoreceptor and pigment epithelial function. The prevalence of retinitis pigmentosa is between 1/3000 and 1/5000 making it one of the most common causes of visual impairment in all age groups.
Roberta A Pagon
exaly +3 more sources
Retinitis Pigmentosa and Retinal Neovascularization
Ophthalmology, 1986Four patients with retinitis pigmentosa and either disc or peripheral retinal neovascularization with recurrent vitreous hemorrhage are described. One patient with peripheral retinal neovascularization also had rubeosis and neovascular glaucoma. The effects of relative hyperoxia on the retinal microcirculation in retinitis pigmentosa as well as ...
Z J Gregor, Alan C Bird
exaly +3 more sources
Survey of Ophthalmology, 1976
The authors review the symptomatic and genetic aspects of the various entities of isolated retinitis pigmentosa (R.P), both in its typical form and in the forms associated with the affection of other ocular tissues. Syndromes in which R. P. is associated with the affection of other organs and systemic disorders are also cconsidered.
S, Merin, E, Auerbach
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The authors review the symptomatic and genetic aspects of the various entities of isolated retinitis pigmentosa (R.P), both in its typical form and in the forms associated with the affection of other ocular tissues. Syndromes in which R. P. is associated with the affection of other organs and systemic disorders are also cconsidered.
S, Merin, E, Auerbach
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Trends in Genetics, 2005
Retinitis pigmentosa (RP) is one of the most genetically heterogeneous inherited disorders. Twelve genes have now been identified in the autosomal dominant form of the disease, including some recently characterized genes that show unprecedented and fascinating traits in both their function and in their expression profiles.
Avril, Kennan +2 more
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Retinitis pigmentosa (RP) is one of the most genetically heterogeneous inherited disorders. Twelve genes have now been identified in the autosomal dominant form of the disease, including some recently characterized genes that show unprecedented and fascinating traits in both their function and in their expression profiles.
Avril, Kennan +2 more
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Unilateral Retinitis Pigmentosa
Archives of Ophthalmology, 1973Seven cases of unilateral retinal pigmentary degeneration are presented including five of unknown cause and two which developed following ophthalmic artery occlusion. Ophthalmoscopic and functional findings were similar in all of these patients, strongly suggesting a vascular cause for this disease.
R E, Carr, I M, Siegel
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SYMPATHECTOMY FOR RETINITIS PIGMENTOSA
Archives of Ophthalmology, 1935In September 1930, Royle1stimulated interest in the treatment of retinitis pigmentosa by stating that the vision of patients with this disease could be improved by the surgical interruption of the sympathetic nerves to the eye. Our experience with this form of treatment has been limited to four cases.
A E, Macdonald, K G, McKenzie
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Etiology of Retinitis Pigmentosa
2022Retinitis pigmentosa (RP) is a set of symptoms including tunnel vision, night blindness, and progressive vision loss, stemming from a very heterogeneous set of causes-it can result from a several different kinds of mutations (non-syndromic) in conjunction with other symptoms, as part of a larger syndrome (syndromic), or secondary to an organ system ...
Mark P, Breazzano +3 more
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Archives of Ophthalmology, 1978
A total of 174 patients (347 eyes) with retinitis pigmentosa were categorized by genetic type and assessed as to the degree of central visual loss. The degree of central visual loss was mildest in cases of autosomal-dominant inheritance and most extensive in cases of X-linked recessive inheritance.
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A total of 174 patients (347 eyes) with retinitis pigmentosa were categorized by genetic type and assessed as to the degree of central visual loss. The degree of central visual loss was mildest in cases of autosomal-dominant inheritance and most extensive in cases of X-linked recessive inheritance.
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Optometry and Vision Science, 1998
ABSTRACT: Background. Retinitis pigmentosa (RP) is one of the most common inherited retinal diseases, with a prevalence of about 1 in 3500 to 4500. Retinitis pigmentosa inversa is a rare variant of this disorder characterized by areas of choroidal degeneration with pigment migration and bony spicule formation in the macular area.
S, Ferrucci +2 more
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ABSTRACT: Background. Retinitis pigmentosa (RP) is one of the most common inherited retinal diseases, with a prevalence of about 1 in 3500 to 4500. Retinitis pigmentosa inversa is a rare variant of this disorder characterized by areas of choroidal degeneration with pigment migration and bony spicule formation in the macular area.
S, Ferrucci +2 more
openaire +2 more sources