Zobrazeno 1 - 6
of 6
pro vyhledávání: '"S A, Madreperla"'
Publikováno v:
Ophthalmic Paediatrics and Genetics. 12:49-56
Genesis of the childhood ocular tumor retinoblastoma results from the mutational inactivation of a single gene, RB, located on chromosome 13. Cultured cells or cell lines derived from retinoblastomas have been extensively studied for insight into mut
Publikováno v:
Ophthalmology. 104(11)
Choroidal hemangioma is a benign hamartoma that causes accumulation of subretinal fluid and resultant visual loss. Although photocoagulation can result in resolution of subretinal fluid, some have found that recurrence is common and final visual acui
Autor:
S A, Madreperla, B W, McCuen
Publikováno v:
Retina (Philadelphia, Pa.). 15(2)
Silicone oil tamponade is used in treating retinal detachments, but silicone-associated complications remain frequent. Keratopathy and acute pupillary block glaucoma are related to migration of silicone oil into the anterior chamber. Since 1985, many
Autor:
S A, Madreperla
Publikováno v:
Ophthalmic paediatrics and genetics. 14(2)
Olivopontocerebellar atrophy with retinal degeneration (OPCA type III) and autosomal dominant cerebellar atrophy of late onset (type II) appear to represent the same disease which is characterized by dominantly inherited cerebellar ataxia and pigment
Publikováno v:
Cancer research. 51(23 Pt 1)
Human retinoblastoma is caused by mutational inactivation of the retinoblastoma suppressor gene (RB). We have examined intraocular tumorigenicity of retinoblastoma cells in which RB expression was achieved by retroviral transduction. Retinoblastoma c
Autor:
R, Adler, S A, Madreperla
Publikováno v:
Advances in experimental medicine and biology. 265