Results 191 to 200 of about 53,967 (228)
Some of the next articles are maybe not open access.
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.
openaire +2 more sources
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
openaire +1 more source
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
openaire +1 more source
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
openaire +1 more source
David G. Birch, Abigail Fahim
openaire +1 more source
Antisense oligonucleotide-based treatment of retinitis pigmentosa caused by USH2A exon 13 mutations
Molecular Therapy, 2021Ralph Slijkerman +2 more
exaly
Retinitis Pigmentosa (? Pseudo-)
Proceedings of the Royal Society of Medicine, 1924openaire +2 more sources