Arch Ophthalmol -- Table of Contents (Vol. 111 No. 11, November 1993)

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Table of Contents

ARTICLES

Vitamin A supplementation for retinitis pigmentosa
E. L. Berson; B. Rosner; M. A. Sandberg; K. C. Hayes; B. W. Nicholson; C. Weigel-DiFrano; W. Willett
Arch Ophthalmol. 1993;111:1456-1459.

A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa
E. W. Norton
Arch Ophthalmol. 1993;111:1460.

A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa
M. F. Marmor
Arch Ophthalmol. 1993;111:1460-1461.

A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa
D. D. Clowes
Arch Ophthalmol. 1993;111:1461-1462.

A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa
J. W. Gamel; C. C. Barr
Arch Ophthalmol. 1993;111:1462-1463.

A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa
A. R. Fielder
Arch Ophthalmol. 1993;111:1463.

Combined obstruction of the central retinal artery and vein associated with meningeal carcinomatosis
E. R. Schaible; K. C. Golnik
Arch Ophthalmol. 1993;111:1467-1468.

Endogenous endophthalmitis caused by Propionibacterium acnes
J. de la Fuente; P. Fernandez-Catalina; B. Sopena; L. Cadarso
Arch Ophthalmol. 1993;111:1468.

Preparing for managed competition. Utilization of ophthalmologic services varies by state
J. C. Javitt; Y. P. Chiang
Arch Ophthalmol. 1993;111:1469-1470.

Ocular gene therapy. From fantasy to foreseeable reality
D. J. Zack
Arch Ophthalmol. 1993;111:1477-1479.

Clinical physiology of heritable photoreceptor diseases
A. B. Fulton; M. E. Breton
Arch Ophthalmol. 1993;111:1479-1481.

Leber's hereditary optic neuropathy masquerading as tobacco-alcohol amblyopia
M. E. Cullom; K. L. Heher; N. R. Miller; P. J. Savino; D. R. Johns
Arch Ophthalmol. 1993;111:1482-1485.
ABSTRACT

Heteroplasmy in Leber's hereditary optic neuropathy
K. H. Smith; D. R. Johns; K. L. Heher; N. R. Miller
Arch Ophthalmol. 1993;111:1486-1490.
ABSTRACT

Identical twins who are discordant for Leber's hereditary optic neuropathy
D. R. Johns; K. H. Smith; N. R. Miller; M. E. Sulewski; W. B. Bias
Arch Ophthalmol. 1993;111:1491-1494.
ABSTRACT

A maculopathy associated with the 15257 mitochondrial DNA mutation
K. L. Heher; D. R. Johns
Arch Ophthalmol. 1993;111:1495-1499.
ABSTRACT

Natural course of visual functions in the Bardet-Biedl syndrome
A. B. Fulton; R. M. Hansen; R. J. Glynn
Arch Ophthalmol. 1993;111:1500-1506.
ABSTRACT

Pseudo low penetrance in retinoblastoma. Fortuitous familial aggregation of sporadic cases caused by independently derived mutations in two large pedigrees
F. L. Munier; M. X. Wang; M. A. Spence; F. Thonney; A. Balmer; G. Pescia; L. A. Donoso; A. L. Murphree
Arch Ophthalmol. 1993;111:1507-1511.
ABSTRACT

A new codon 15 rhodopsin gene mutation in autosomal dominant retinitis pigmentosa is associated with sectorial disease
L. J. Sullivan; G. S. Makris; P. Dickinson; L. E. Mulhall; S. Forrest; R. G. Cotton; M. S. Loughnan
Arch Ophthalmol. 1993;111:1512-1517.
ABSTRACT

Dominant retinitis pigmentosa associated with two rhodopsin gene mutations. Leu-40-Arg and an insertion disrupting the 5'-splice junction of exon 5
R. Y. Kim; M. al-Maghtheh; F. W. Fitzke; G. B. Arden; M. Jay; S. S. Bhattacharya; A. C. Bird
Arch Ophthalmol. 1993;111:1518-1524.
ABSTRACT

Variable retinal and neurologic manifestations in patients harboring the mitochondrial DNA 8993 mutation
R. G. Ortiz; N. J. Newman; J. M. Shoffner; A. E. Kaufman; D. A. Koontz; D. C. Wallace
Arch Ophthalmol. 1993;111:1525-1530.
ABSTRACT

Phenotypic variation including retinitis pigmentosa, pattern dystrophy, and fundus flavimaculatus in a single family with a deletion of codon 153 or 154 of the peripherin/RDS gene
R. G. Weleber; R. E. Carr; W. H. Murphey; V. C. Sheffield; E. M. Stone
Arch Ophthalmol. 1993;111:1531-1542.
ABSTRACT

A new syndrome of myelinated nerve fibers, vitreoretinopathy, and skeletal malformations
E. I. Traboulsi; J. I. Lim; R. Pyeritz; H. K. Goldberg; J. A. Haller
Arch Ophthalmol. 1993;111:1543-1545.
ABSTRACT

Phenotypic variation in combined granular-lattice (Avellino) corneal dystrophy
G. O. Rosenwasser; B. M. Sucheski; N. Rosa; B. Pastena; A. Sebastiani; J. W. Sassani; H. D. Perry
Arch Ophthalmol. 1993;111:1546-1552.
ABSTRACT

Identification of a nonsense mutation at codon 128 of the Norrie's disease gene in a male infant
F. Wong; M. F. Goldberg; Y. Hao
Arch Ophthalmol. 1993;111:1553-1557.
ABSTRACT

Negative-configuration electroretinogram in Oregon eye disease. Consistent phenotype in Xp21 deletion syndrome
D. A. Pillers; W. K. Seltzer; B. R. Powell; P. N. Ray; F. Tremblay; G. R. La Roche; R. A. Lewis; E. R. McCabe; A. W. Eriksson; R. G. Weleber
Arch Ophthalmol. 1993;111:1558-1563.
ABSTRACT

Lifetime prevalence of ocular injuries from the Baltimore Eye Survey
J. Katz; J. M. Tielsch
Arch Ophthalmol. 1993;111:1564-1568.
ABSTRACT

Hyaloid vessels of the human fetal eye. A scanning electron microscopic study of corrosion casts
W. Strek; P. Strek; M. Nowogrodzka-Zagorska; J. A. Litwin; K. Pitynski; A. J. Miodonski
Arch Ophthalmol. 1993;111:1573-1577.
ABSTRACT

Orbital fat prolapse
D. R. Jordan
Arch Ophthalmol. 1993;111:1583.