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Optometry - Journal of the American Optometric Association, 2005
Retinitis pigmentosa (RP) is one of the most common hereditary retinal dystrophies and causes of visual impairment affecting all age groups. The reported incidence varies, but is considered to be between 1 in 3,000 to 1 in 7,000. Sector retinitis pigmentosa is an atypical form of RP that is characterized by regionalized areas of bone spicule ...
Craig, Van Woerkom, Steven, Ferrucci
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Retinitis pigmentosa (RP) is one of the most common hereditary retinal dystrophies and causes of visual impairment affecting all age groups. The reported incidence varies, but is considered to be between 1 in 3,000 to 1 in 7,000. Sector retinitis pigmentosa is an atypical form of RP that is characterized by regionalized areas of bone spicule ...
Craig, Van Woerkom, Steven, Ferrucci
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Genetic characteristics of retinitis pigmentosa in 1204 Japanese patients
Journal of Medical Genetics, 2019Background The genetic profile of retinitis pigmentosa (RP) in East Asian populations has not been well characterised. Therefore, we conducted a large-scale sequencing study to investigate the genes and variants causing RP in a Japanese population ...
Y. Koyanagi +26 more
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Optometry and Vision Science, 1998
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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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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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.
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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.
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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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Retinitis Pigmentosa: Review of Current Treatment.
International ophthalmology clinics, 2019Retinitis pigmentosa (RP) is a diverse group of hereditary degenerations characterized by progressive dysfunction of predominantly rod followed by cone photoreceptors.
Angeline L. Wang +3 more
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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 ...
A E, Uliss, Z J, Gregor, A C, Bird
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Classification of disease severity in retinitis pigmentosa
British Journal of Ophthalmology, 2019Aim To develop a simple and easily applicable classification of disease severity in retinitis pigmentosa (RP). Methods This is a retrospective cross-sectional study.
Mustafa Iftikhar +6 more
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2018
X-linked retinitis pigmentosa (XLRP) is considered to be one of the most severe forms of retinitis pigmentosa (RP). It accounts for about 6-20% of all RP cases, including about 10% in the United States and 25% in England.
Stephen H, Tsang, Tarun, Sharma
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X-linked retinitis pigmentosa (XLRP) is considered to be one of the most severe forms of retinitis pigmentosa (RP). It accounts for about 6-20% of all RP cases, including about 10% in the United States and 25% in England.
Stephen H, Tsang, Tarun, Sharma
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Retinitis pigmentosa: recent advances and future directions in diagnosis and management
Current opinion in pediatrics, 2018Purpose of review Retinitis pigmentosa is a group of genetically diverse inherited blinding disorders for which there are no treatments. Owing to recent advances in imaging technology, DNA sequencing, gene therapy, and stem cell biology, clinical trials ...
Abigail T. Fahim
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