Zobrazeno 1 - 7
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pro vyhledávání: '"J D, Kivlin"'
Autor:
J D, Kivlin
Publikováno v:
Transactions of the American Ophthalmological Society. 97
PURPOSE: To examine the ophthalmologic experience with the shaken baby syndrome (SBS) at one medical center, including clinical findings, autopsy findings, and the visual outcome of survivors. METHODS: One hundred sixteen patients admitted from 1987
Autor:
J D, Kivlin, A W, Biglan, R A, Gordon, V, Dobson, R A, Hardy, E A, Palmer, B, Tung, W, Gilbert, R, Spencer, K P, Cheng, E, Buckley
Publikováno v:
Archives of ophthalmology (Chicago, Ill. : 1960). 114(2)
To determine whether the extent of retinal vessel development present on early screening examinations for retinopathy of prematurity has prognostic value?The prospectively collected data from the Multicenter Trial of Cryotherapy for Retinopathy of Pr
Autor:
J D, Kivlin, M E, Wilson
Publikováno v:
Journal of pediatric ophthalmology and strabismus. 32(1)
Fewer than 15 cases of cellulitis and subconjunctival abscess after extraocular muscle surgery have been reported in detail. In an effort to provide greater information about this serious complication, the members of the American Association for Pedi
Publikováno v:
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie. 29(4)
Autor:
J B, Bateman, T L, Kojis, R M, Cantor, C, Heinzmann, J T, Ngo, M A, Spence, G, Inana, J D, Kivlin, D, Curtis, R S, Sparkes
Publikováno v:
Transactions of the American Ophthalmological Society. 91
Norrie disease is a rare disease of newborn males caused by prenatal or perinatal retinal detachment, which may be associated with mental retardation, psychosis, and/or hearing loss. DXS7 (L1.28) and MAO A and B loci have been linked to the ND locus
Publikováno v:
Ophthalmology. 93(1)
We studied the eyes of a 51-year-old man with the clinical diagnosis of fundus flavimaculatus without macular involvement by light and electron microscopy. Scanning and transmission electron microscopy revealed elevated aggregates of enlarged retinal
Publikováno v:
American journal of human genetics. 35(6)
A kindred of German descent was studied for dominant optic atrophy, type Kjer (McKusick catalog no. 16540). One hundred twenty-three family members were examined clinically, and 36 affected, 81 normal, and six uncertain members were ascertained. Twen