71 related articles for article (PubMed ID: 15767907)
1. [Hereditary macular dystrophies].
Rozet JM; Gerber S; Ducroq D; Hamel C; Dufier JL; Kaplan J
J Fr Ophtalmol; 2005 Jan; 28(1):113-24. PubMed ID: 15767907
[TBL] [Abstract][Full Text] [Related]
2. Cone rod dystrophies.
Hamel CP
Orphanet J Rare Dis; 2007 Feb; 2():7. PubMed ID: 17270046
[TBL] [Abstract][Full Text] [Related]
3. Inherited macular dystrophies and differential diagnostics.
Liutkevičienė R; Lesauskaitė V; Ašmonienė V; Gelžinis A; Zaliūnienė D; Jašinskas V
Medicina (Kaunas); 2012; 48(9):485-95. PubMed ID: 23168924
[TBL] [Abstract][Full Text] [Related]
4. The genetics of inherited macular dystrophies.
Michaelides M; Hunt DM; Moore AT
J Med Genet; 2003 Sep; 40(9):641-50. PubMed ID: 12960208
[TBL] [Abstract][Full Text] [Related]
5. High-resolution in vivo imaging of the RPE mosaic in eyes with retinal disease.
Roorda A; Zhang Y; Duncan JL
Invest Ophthalmol Vis Sci; 2007 May; 48(5):2297-303. PubMed ID: 17460294
[TBL] [Abstract][Full Text] [Related]
6. Patterned anomalies of the retinal pigment epithelium: dystrophy or syndrome?
Bastiaensen LA; Hoefnagels KL
Doc Ophthalmol; 1983 Feb; 55(1-2):17-29. PubMed ID: 6839931
[TBL] [Abstract][Full Text] [Related]
7. Gene therapy for retinal degeneration.
Reichel MB; Ali RR; Hunt DM; Bhattacharya SS
Ophthalmic Res; 1997; 29(5):261-8. PubMed ID: 9323717
[TBL] [Abstract][Full Text] [Related]
8. Recent advances in the genetics of macular dystrophies.
Mah DY; Wong PW; Edwards A; MacDonald IM
Can J Ophthalmol; 1998 Apr; 33(3):135-43. PubMed ID: 9606569
[No Abstract] [Full Text] [Related]
9. The challenge of modeling macular degeneration in mice.
Marmorstein AD; Marmorstein LY
Trends Genet; 2007 May; 23(5):225-31. PubMed ID: 17368622
[TBL] [Abstract][Full Text] [Related]
10. Patterned dystrophies of the retinal pigment epithelium.
Hsieh RC; Fine BS; Lyons JS
Arch Ophthalmol; 1977 Mar; 95(3):429-35. PubMed ID: 843272
[TBL] [Abstract][Full Text] [Related]
11. [Identification of the molecular bases of retinal dystrophies: two divergent situations and their implications].
Rozet JM
Bull Acad Natl Med; 2009 Jan; 193(1):163-77; discussion 177-8. PubMed ID: 19718988
[TBL] [Abstract][Full Text] [Related]
12. Genotype-phenotype correlations and differential diagnosis in autosomal dominant macular disease.
Iannaccone A
Doc Ophthalmol; 2001 May; 102(3):197-236. PubMed ID: 11556486
[TBL] [Abstract][Full Text] [Related]
13. The spectrum of retinal phenotypes caused by mutations in the ABCA4 gene.
Klevering BJ; Deutman AF; Maugeri A; Cremers FP; Hoyng CB
Graefes Arch Clin Exp Ophthalmol; 2005 Feb; 243(2):90-100. PubMed ID: 15614537
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 1562260
[TBL] [Abstract][Full Text] [Related]
15. Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1).
Gehrig A; Felbor U; Kelsell RE; Hunt DM; Maumenee IH; Weber BH
J Med Genet; 1998 Aug; 35(8):641-5. PubMed ID: 9719369
[TBL] [Abstract][Full Text] [Related]
16. Expression and characterization of peripherin/rds-rom-1 complexes and mutants implicated in retinal degenerative diseases.
Goldberg AF; Molday RS
Methods Enzymol; 2000; 316():671-87. PubMed ID: 10800708
[TBL] [Abstract][Full Text] [Related]
17. [Retinitis pigmentosa--clinical, genetic and pathophysiologic aspects].
Jurklies B; Zrenner E; Wessing A
Klin Monbl Augenheilkd; 1997 Jan; 210(1):1-18. PubMed ID: 9206727
[TBL] [Abstract][Full Text] [Related]
18. Molecular genetics of human retinal dystrophies.
Inglehearn CF
Eye (Lond); 1998; 12 ( Pt 3b)():571-9. PubMed ID: 9775219
[TBL] [Abstract][Full Text] [Related]
19. Genetic and molecular studies of macular dystrophies: recent developments.
Zhang K; Nguyen TH; Crandall A; Donoso LA
Surv Ophthalmol; 1995; 40(1):51-61. PubMed ID: 8545803
[TBL] [Abstract][Full Text] [Related]
20. [Pattern dystrophies and intrafamilial phenotypic variation].
Bernasconi OR; Piguet B
Klin Monbl Augenheilkd; 1996 May; 208(5):291-3. PubMed ID: 8766030
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]