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Exudative Retinitis pigmentosa
Ophthalmologica, 1988Six persons with retinitis pigmentosa and exudative vasculopathy were observed within a group of 110 patients with retinitis pigmentosa seen during 5 years. Two new hypotheses are formulated in order to explain the origin of this relationship.
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2012
Abstract Retinitis pigmentosa (RP) is the name given to a heterogeneous group of genetic diseases sharing a common phenotype. Traditionally, RP is a progressive rod–cone dystrophy characterized by nyctalopia, peripheral visual field loss, and loss of the rod electroretinogram (ERG) response.
Henry A. Ferreyra, John R. Heckenlively
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Abstract Retinitis pigmentosa (RP) is the name given to a heterogeneous group of genetic diseases sharing a common phenotype. Traditionally, RP is a progressive rod–cone dystrophy characterized by nyctalopia, peripheral visual field loss, and loss of the rod electroretinogram (ERG) response.
Henry A. Ferreyra, John R. Heckenlively
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Abstract Retinitis pigmentosa (RP) is a heterogeneous group of genetic diseases sharing a common phenotype that includes nyctalopia and visual field loss. In the past 30 years, the number of identified genes associated with RP has grown to over 140.
David G. Birch, Abigail Fahim
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David G. Birch, Abigail Fahim
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Retinitis Pigmentosa (? Pseudo-)
Proceedings of the Royal Society of Medicine, 1924openaire +2 more sources