Kimura AE - Search Results

1

Procollagen II gene mutation in Stickler syndrome.

Brown DM, Nichols BE, Weingeist TA, Sheffield VC, Kimura AE, Stone EM. Brown DM, et al. Among authors: kimura ae. Arch Ophthalmol. 1992 Nov;110(11):1589-93. doi: 10.1001/archopht.1992.01080230089027. Arch Ophthalmol. 1992. PMID: 1444917

2

Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13.

Stone EM, Kimura AE, Folk JC, Bennett SR, Nichols BE, Streb LM, Sheffield VC. Stone EM, et al. Among authors: kimura ae. Hum Mol Genet. 1992 Dec;1(9):685-9. doi: 10.1093/hmg/1.9.685. Hum Mol Genet. 1992. PMID: 1284594

3

Ocular findings associated with rhodopsin gene codon 17 and codon 182 transition mutations in dominant retinitis pigmentosa.

Fishman GA, Stone EM, Sheffield VC, Gilbert LD, Kimura AE. Fishman GA, et al. Among authors: kimura ae. Arch Ophthalmol. 1992 Jan;110(1):54-62. doi: 10.1001/archopht.1992.01080130056026. Arch Ophthalmol. 1992. PMID: 1731723

4

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. Among authors: kimura ae. Ophthalmology. 1991 Dec;98(12):1806-13. doi: 10.1016/s0161-6420(91)32046-3. Ophthalmology. 1991. PMID: 1775314

5

Novel frameshift mutations in the procollagen 2 gene (COL2A1) associated with Stickler syndrome (hereditary arthro-ophthalmopathy).

Brown DM, Vandenburgh K, Kimura AE, Weingeist TA, Sheffield VC, Stone EM. Brown DM, et al. Among authors: kimura ae. Hum Mol Genet. 1995 Jan;4(1):141-2. doi: 10.1093/hmg/4.1.141. Hum Mol Genet. 1995. PMID: 7711727 No abstract available.

6

Genetic linkage of Wagner disease and erosive vitreoretinopathy to chromosome 5q13-14.

Brown DM, Graemiger RA, Hergersberg M, Schinzel A, Messmer EP, Niemeyer G, Schneeberger SA, Streb LM, Taylor CM, Kimura AE, et al. Brown DM, et al. Among authors: kimura ae. Arch Ophthalmol. 1995 May;113(5):671-5. doi: 10.1001/archopht.1995.01100050139045. Arch Ophthalmol. 1995. PMID: 7748141

7

Ocular findings associated with a Cys39Arg mutation in the Norrie disease gene.

Joos KM, Kimura AE, Vandenburgh K, Bartley JA, Stone EM. Joos KM, et al. Among authors: kimura ae. Arch Ophthalmol. 1994 Dec;112(12):1574-9. doi: 10.1001/archopht.1994.01090240080029. Arch Ophthalmol. 1994. PMID: 7993212

8

Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q.

Stone EM, Nichols BE, Kimura AE, Weingeist TA, Drack A, Sheffield VC. Stone EM, et al. Among authors: kimura ae. Arch Ophthalmol. 1994 Jun;112(6):765-72. doi: 10.1001/archopht.1994.01090180063036. Arch Ophthalmol. 1994. PMID: 8002834

9

Erosive vitreoretinopathy. A new clinical entity.

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

10

Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene.

Nichols BE, Sheffield VC, Vandenburgh K, Drack AV, Kimura AE, Stone EM. Nichols BE, et al. Among authors: kimura ae. Nat Genet. 1993 Mar;3(3):202-7. doi: 10.1038/ng0393-202. Nat Genet. 1993. PMID: 8485574

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