Stone EM - Search Results

1

Differential macular and peripheral expression of bestrophin in human eyes and its implication for best disease.

Mullins RF, Kuehn MH, Faidley EA, Syed NA, Stone EM. Mullins RF, et al. Among authors: stone em. Invest Ophthalmol Vis Sci. 2007 Jul;48(7):3372-80. doi: 10.1167/iovs.06-0868. Invest Ophthalmol Vis Sci. 2007. PMID: 17591911

2

Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13.

Stone EM, Nichols BE, Streb LM, Kimura AE, Sheffield VC. Stone EM, et al. Nat Genet. 1992 Jul;1(4):246-50. doi: 10.1038/ng0792-246. Nat Genet. 1992. PMID: 1302019

3

Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin gene.

Stone EM, Kimura AE, Nichols BE, Khadivi P, Fishman GA, Sheffield VC. Stone EM, et al. Ophthalmology. 1991 Dec;98(12):1806-13. doi: 10.1016/s0161-6420(91)32046-3. Ophthalmology. 1991. PMID: 1775314

4

Best's vitelliform dystrophy.

Blodi CF, Stone EM. Blodi CF, et al. Among authors: stone em. Ophthalmic Paediatr Genet. 1990 Mar;11(1):49-59. Ophthalmic Paediatr Genet. 1990. PMID: 2190134 Review.

5

A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration.

Gorin MB, Jackson KE, Ferrell RE, Sheffield VC, Jacobson SG, Gass JD, Mitchell E, Stone EM. Gorin MB, et al. Among authors: stone em. Ophthalmology. 1995 Feb;102(2):246-55. doi: 10.1016/s0161-6420(95)31029-9. Ophthalmology. 1995. PMID: 7862413 Free article.

6

RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor function.

Kemp CM, Jacobson SG, Cideciyan AV, Kimura AE, Sheffield VC, Stone EM. Kemp CM, et al. Among authors: stone em. Invest Ophthalmol Vis Sci. 1994 Jul;35(8):3154-62. Invest Ophthalmol Vis Sci. 1994. PMID: 8045710

7

Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosa.

Fishman GA, Stone E, Gilbert LD, Vandenburgh K, Sheffield VC, Heckenlively JR. Fishman GA, et al. Ophthalmology. 1994 Aug;101(8):1409-21. doi: 10.1016/s0161-6420(94)31156-0. Ophthalmology. 1994. PMID: 8058286

8

Erosive vitreoretinopathy. A new clinical entity.

Brown DM, Kimura AE, Weingeist TA, Stone EM. Brown DM, et al. Among authors: stone em. Ophthalmology. 1994 Apr;101(4):694-704. doi: 10.1016/s0161-6420(94)31276-0. Ophthalmology. 1994. PMID: 8152765

9

Photoreceptor function in heterozygotes with insertion or deletion mutations in the RDS gene.

Jacobson SG, Cideciyan AV, Kemp CM, Sheffield VC, Stone EM. Jacobson SG, et al. Among authors: stone em. Invest Ophthalmol Vis Sci. 1996 Jul;37(8):1662-74. Invest Ophthalmol Vis Sci. 1996. PMID: 8675410

10

Sub-retinal pigment epithelial deposits in a dominant late-onset retinal degeneration.

Kuntz CA, Jacobson SG, Cideciyan AV, Li ZY, Stone EM, Possin D, Milam AH. Kuntz CA, et al. Among authors: stone em. Invest Ophthalmol Vis Sci. 1996 Aug;37(9):1772-82. Invest Ophthalmol Vis Sci. 1996. PMID: 8759344

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

622 results

Search Page

Filters