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Items: 1 to 20 of 267

1.

Clinical features of progressive bifocal chorioretinal atrophy: a retinal dystrophy linked to chromosome 6q.

Godley BF, Tiffin PA, Evans K, Kelsell RE, Hunt DM, Bird AC.

Ophthalmology. 1996 Jun;103(6):893-8.

PMID:
8643244
2.

Autosomal dominant macular atrophy at 6q14 excludes CORD7 and MCDR1/PBCRA loci.

Griesinger IB, Sieving PA, Ayyagari R.

Invest Ophthalmol Vis Sci. 2000 Jan;41(1):248-55.

PMID:
10634627
3.

Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6q.

Kelsell RE, Godley BF, Evans K, Tiffin PA, Gregory CY, Plant C, Moore AT, Bird AC, Hunt DM.

Hum Mol Genet. 1995 Sep;4(9):1653-6.

PMID:
8541856
5.

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.

Arch Ophthalmol. 1994 Jun;112(6):765-72.

PMID:
8002834
6.

Autosomal dominant macular dystrophy simulating North Carolina macular dystrophy.

Holz FG, Evans K, Gregory CY, Bhattacharya S, Bird AC.

Arch Ophthalmol. 1995 Feb;113(2):178-84.

PMID:
7864750
7.

A reappraisal of the clinical spectrum of North Carolina macular dystrophy.

Khurana RN, Sun X, Pearson E, Yang Z, Harmon J, Goldberg MF, Zhang K.

Ophthalmology. 2009 Oct;116(10):1976-83. doi: 10.1016/j.ophtha.2009.03.028. Epub 2009 Jul 18.

PMID:
19616854
8.

Clinical spectrum of chromosome 6-linked autosomal dominant drusen and macular degeneration.

Stefko ST, Zhang K, Gorin MB, Traboulsi EI.

Am J Ophthalmol. 2000 Aug;130(2):203-8.

PMID:
11004295
9.

Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14.

Edwards AO, Miedziak A, Vrabec T, Verhoeven J, Acott TS, Weleber RG, Donoso LA.

Am J Ophthalmol. 1999 Apr;127(4):426-35.

PMID:
10218695
10.

Dominant cystoid macular dystrophy.

Saksens NT, van Huet RA, van Lith-Verhoeven JJ, den Hollander AI, Hoyng CB, Boon CJ.

Ophthalmology. 2015 Jan;122(1):180-91. doi: 10.1016/j.ophtha.2014.07.053. Epub 2014 Sep 26.

PMID:
25267528
11.

Sorsby's fundus dystrophy.

Hamilton WK, Ewing CC, Ives EJ, Carruthers JD.

Ophthalmology. 1989 Dec;96(12):1755-62. Review.

PMID:
2695876
12.

North Carolina macular dystrophy and central areolar pigment epithelial dystrophy. One family, one disease.

Small KW, Hermsen V, Gurney N, Fetkenhour CL, Folk JC.

Arch Ophthalmol. 1992 Apr;110(4):515-8.

PMID:
1562260
13.

Indocyanine green angiography in Sorsby's fundus dystrophy.

Lafaut BA, De Backer E, Kohno T, De Laey JJ, Meire FM.

Graefes Arch Clin Exp Ophthalmol. 2000 Feb;238(2):158-62.

PMID:
10766286
14.

Clinical and electroretinographic findings of female carriers and affected males in a progressive X-linked cone-rod dystrophy (COD-1) pedigree.

Brown J Jr, Kimura AE, Gorin MB.

Ophthalmology. 2000 Jun;107(6):1104-10. Erratum in: Ophthalmology 2000 Aug;107(8):1440.

PMID:
10857830
15.

Thirty-Year follow-up of an African American family with macular dystrophy of the retina, locus 1 (North Carolina macular dystrophy).

Kiernan DF, Shah RJ, Hariprasad SM, Grassi MA, Small KW, Kiernan JP, Mieler WF.

Ophthalmology. 2011 Jul;118(7):1435-43. doi: 10.1016/j.ophtha.2010.10.041. Epub 2011 Feb 18.

PMID:
21310494
16.

A new locus for dominant drusen and macular degeneration maps to chromosome 6q14.

Kniazeva M, Traboulsi EI, Yu Z, Stefko ST, Gorin MB, Shugart YY, O'Connell JR, Blaschak CJ, Cutting G, Han M, Zhang K.

Am J Ophthalmol. 2000 Aug;130(2):197-202.

17.

Clinical and genetic studies of an autosomal dominant cone-rod dystrophy with features of Stargardt disease.

Kniazeva MF, Chiang MF, Cutting GR, Zack DJ, Han M, Zhang K.

Ophthalmic Genet. 1999 Jun;20(2):71-81.

PMID:
10420191
18.

Clinical and genetic evidence for autosomal dominant North Carolina macular dystrophy in a German family.

Pauleikhoff D, Sauer CG, Müller CR, Radermacher M, Merz A, Weber BH.

Am J Ophthalmol. 1997 Sep;124(3):412-5.

PMID:
9439376
19.

Genetic and phenotypic heterogeneity in pattern dystrophy.

Francis PJ, Schultz DW, Gregory AM, Schain MB, Barra R, Majewski J, Ott J, Acott T, Weleber RG, Klein ML.

Br J Ophthalmol. 2005 Sep;89(9):1115-9.

20.

Congenital-onset central chorioretinal dystrophy associated with high myopia.

Iqbal M, Jalili IK.

Eye (Lond). 1998;12 ( Pt 2):260-5.

PMID:
9683951

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