Results 91 to 100 of about 6,211 (169)

Autosomal dominant Riggs-type congenital stationary night blindness with fundus sheen and retinal atrophy due to a novel GNAT1 p.Gln200Arg variant. [PDF]

open access: yesDoc Ophthalmol
Chou JJ   +7 more
europepmc   +1 more source

UVEAL EFFUSION IN WALDENSTRÖM MACROGLOBULINEMIA: A CASE REPORT. [PDF]

open access: yesRetin Cases Brief Rep
Darmon J   +4 more
europepmc   +1 more source

[The fundus oculi in diabetes].

open access: yesRevista medica de Chile, 1998
H, FRITSCHE   +6 more
openaire   +1 more source

Benign foveal retinal pigment epithelium hypopigmentation without functional loss : pediatric case series. [PDF]

open access: yesGraefes Arch Clin Exp Ophthalmol
Boulert E   +4 more
europepmc   +1 more source

Retinal pigment epithelial tears associated with idiopathic central serous chorioretinopathy

open access: yesIndian Journal of Ophthalmology, 2000
Shanmugam Mahesh, Bhende Muna
doaj  

Home - About - Disclaimer - Privacy