Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Jose Miguel Risco"'
Publikováno v:
Ophthalmology. 102:186-192
Background: Three children, ranging in age from 2 to 6 months, had diffuse and homogeneously opaque corneas, clinically consistent with congenital hereditary endothelial dystrophy. Bilateral elevated intraocular pressure (IOP) was a feature in all th
Publikováno v:
Archives of ophthalmology (Chicago, Ill. : 1960). 113(9)
Publikováno v:
Archives of ophthalmology (Chicago, Ill. : 1960). 113(4)
Autor:
Jose Miguel Risco, Lynn Millar
Publikováno v:
Ophthalmology. 99(4)
A 40-year-old patient frequently self-administered topical oxybuprocaine drops for approximately 7 days after bilateral ultraviolet-light keratitis. Initially, he developed bilateral chronic epithelial defects with diffuse stromal infiltration and ed
Publikováno v:
Ophthalmology. 98(4)
Patients with keratoglobus and blue sclera as part of a generalized connective tissue disorder are at a high risk of developing corneal perforations either spontaneously or after mild trauma. Six patients (6 eyes) between the ages of 2 and 16 years o
Autor:
Jose Miguel Risco, James A. Cameron
Publikováno v:
American Journal of Ophthalmology. 118:666-667
Autor:
Jose Miguel Risco, Abdulaziz H. Awad
Publikováno v:
American Journal of Ophthalmology. 116:107-108
Autor:
Jose Miguel Risco, Ahmed A. Hidayat
Publikováno v:
Ophthalmology. 96:1203-1211
Sixty-two cases of corneal amyloidosis were studied. The median age of the 48 men and 14 women was 66 years. The patients had bilateral, diffuse corneal opacity extending to the limbus and severe visual impairment. The corneal condition was not famil
Publikováno v:
Archives of ophthalmology (Chicago, Ill. : 1960). 104(1)
• We observed the repair process of the choriocapillaris after confluent argon laser retinal photocoagulation in the domestic cat with a plastic injectioncorrosion technique coupled with scanning electron microscopy and transmission electron micros
Publikováno v:
Journal of pediatric ophthalmology and strabismus. 19(5)
A 10-year-old Afro-American female with SS disease presented with a history of painless loss of vision (RE) of 26 hours duration. Sequential fluorescein angiography revealed bilateral parafoveal occlusions and evidence of prior vaso-occlusions in eac