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Retinitis pigmentosa, pigmentary retinopathies, and neurologic diseases.
Bhatti MT. Bhatti MT. Curr Neurol Neurosci Rep. 2006 Sep;6(5):403-13. doi: 10.1007/s11910-996-0021-z. Curr Neurol Neurosci Rep. 2006. PMID: 16928351 Review.
The pathophysiologic basis of the progressive visual loss in patients with RP is not completely understood but is felt to be due to a primary retinal photoreceptor cell degenerative process mainly affecting the rods of the peripheral retina. In most cases RP is seen in iso …
The pathophysiologic basis of the progressive visual loss in patients with RP is not completely understood but is felt to be due to a primar …
Pigmented paravenous retinochoroidal atrophy. A literature review supported by seven cases.
Kükner AS, Yilmaz T, Celebi S, Aydemir O, Ulaş F. Kükner AS, et al. Ophthalmologica. 2003 Nov-Dec;217(6):436-40. doi: 10.1159/000073076. Ophthalmologica. 2003. PMID: 14573979 Review.
Seven patients (4 men and 3 women, ranging in age from 27 to 64 years) with pigmented paravenous retinochoroidal atrophy, a rare disorder of unknown origin, were studied. ...Both fundi showed patches of retinochoroidal atrophy and pigmentation along the retinal vein …
Seven patients (4 men and 3 women, ranging in age from 27 to 64 years) with pigmented paravenous retinochoroidal atrophy, a rare diso …
Ocular findings in a form of retinitis pigmentosa with a rhodopsin gene defect.
Berson EL. Berson EL. Trans Am Ophthalmol Soc. 1990;88:355-88. Trans Am Ophthalmol Soc. 1990. PMID: 2095030 Free PMC article. Review.
This clinical heterogeneity among patients with the same mutation, with older patients sometimes showing less loss of visual function and less intraretinal bone spicule pigment than younger patients, suggests that some factor other than the gene defect itself …
This clinical heterogeneity among patients with the same mutation, with older patients sometimes showing less loss of visual function and le …
[New drug therapy for retinal degeneration].
Ohguro H. Ohguro H. Nippon Ganka Gakkai Zasshi. 2008 Jan;112(1):7-21. Nippon Ganka Gakkai Zasshi. 2008. PMID: 18240599 Review. Japanese.
Retinitis pigmentosa (RP) is an inherited retinal degeneration characterized by nyctalopia, ring scotoma, and bone-spicule pigmentation of the retina. So far, no effective therapy has been found for RP. As a possible molecular etiology of RP, retina
Retinitis pigmentosa (RP) is an inherited retinal degeneration characterized by nyctalopia, ring scotoma, and bone-spicule