249 related articles for article (PubMed ID: 8759344)
21. Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk gene.
Tschernutter M; Jenkins SA; Waseem NH; Saihan Z; Holder GE; Bird AC; Bhattacharya SS; Ali RR; Webster AR
Br J Ophthalmol; 2006 Jun; 90(6):718-23. PubMed ID: 16714263
[TBL] [Abstract][Full Text] [Related]
22. Cone-rod dystrophy with serpentine-like retinal deposits.
Kellner U
Arch Ophthalmol; 1998 Oct; 116(10):1307-13. PubMed ID: 9790628
[TBL] [Abstract][Full Text] [Related]
23. Extensive intrafamilial and interfamilial phenotypic variation among patients with autosomal dominant retinal dystrophy and mutations in the human RDS/peripherin gene.
Apfelstedt-Sylla E; Theischen M; Rüther K; Wedemann H; Gal A; Zrenner E
Br J Ophthalmol; 1995 Jan; 79(1):28-34. PubMed ID: 7880786
[TBL] [Abstract][Full Text] [Related]
24. Pattern dystrophy of the retinal pigment epithelium and geographic atrophy of the macula.
Marmor MF; McNamara JA
Am J Ophthalmol; 1996 Sep; 122(3):382-92. PubMed ID: 8794711
[TBL] [Abstract][Full Text] [Related]
25. Longitudinal phenotypic study of late-onset retinal degeneration due to a founder variant c.562C>A p.(Pro188Thr) in the
De Zaeytijd J; Coppieters F; De Bruyne M; Van Royen J; Roels D; Six R; Van Cauwenbergh C; De Baere E; Leroy BP
Ophthalmic Genet; 2021 Oct; 42(5):521-532. PubMed ID: 33949280
[No Abstract] [Full Text] [Related]
26. Abnormal dark adaptation and rhodopsin kinetics in Sorsby's fundus dystrophy.
Steinmetz RL; Polkinghorne PC; Fitzke FW; Kemp CM; Bird AC
Invest Ophthalmol Vis Sci; 1992 Apr; 33(5):1633-6. PubMed ID: 1559761
[TBL] [Abstract][Full Text] [Related]
27. Erosive vitreoretinopathy. A new clinical entity.
Brown DM; Kimura AE; Weingeist TA; Stone EM
Ophthalmology; 1994 Apr; 101(4):694-704. PubMed ID: 8152765
[TBL] [Abstract][Full Text] [Related]
28. No pigment deposition in a patient with advanced retinitis punctata albescens.
Fujii M; Hayasaka S
Ophthalmologica; 1994; 208(6):339-41. PubMed ID: 7845653
[TBL] [Abstract][Full Text] [Related]
29. Crystalline retinopathy.
Grizzard WS; Deutman AF; Nijhuis F; de Kerk AA
Am J Ophthalmol; 1978 Jul; 86(1):81-8. PubMed ID: 677237
[TBL] [Abstract][Full Text] [Related]
30. Central areolar pigment epithelial (cape) dystrophy.
Dobbie JG; Fetkenhour CL; Shoch D
Trans Am Ophthalmol Soc; 1975; 73():141-52. PubMed ID: 1246802
[TBL] [Abstract][Full Text] [Related]
31. [Paraneoplastic retinopathy simulating cone dystrophy with achromatopsia].
Cogan DG; Kuwabara T; Currie J; Kattah J
Klin Monbl Augenheilkd; 1990 Aug; 197(2):156-8. PubMed ID: 2243476
[TBL] [Abstract][Full Text] [Related]
32. Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophy.
Jacobson SG; Cideciyan AV; Bennett J; Kingsley RM; Sheffield VC; Stone EM
Arch Ophthalmol; 2002 Mar; 120(3):376-9. PubMed ID: 11879143
[TBL] [Abstract][Full Text] [Related]
33. [Albescent punctate retinopathy with central pigment epithelium atrophy].
Weber U; Hennekes R
Klin Monbl Augenheilkd; 1984 Jan; 184(1):51-4. PubMed ID: 6608625
[TBL] [Abstract][Full Text] [Related]
34. Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX gene.
Tzekov RT; Liu Y; Sohocki MM; Zack DJ; Daiger SP; Heckenlively JR; Birch DG
Invest Ophthalmol Vis Sci; 2001 May; 42(6):1319-27. PubMed ID: 11328746
[TBL] [Abstract][Full Text] [Related]
35. Olivopontocerebellar atrophy with retinal degeneration. An electroretinographic and histopathologic investigation.
To KW; Adamian M; Jakobiec FA; Berson EL
Ophthalmology; 1993 Jan; 100(1):15-23. PubMed ID: 8433819
[TBL] [Abstract][Full Text] [Related]
36. Reticular dystrophy of the retinal pigment epithelium. A clinical and electrophysiologic study of three generations.
Kingham JD; Fenzl RE; Willerson D; Aaberg TM
Arch Ophthalmol; 1978 Jul; 96(7):1177-84. PubMed ID: 666625
[TBL] [Abstract][Full Text] [Related]
37. Pattern dystrophies of the retinal pigment epithelium.
Daniele S; Carbonara A; Daniele C; Restagno G; Orcidi F
Acta Ophthalmol Scand; 1996 Feb; 74(1):51-5. PubMed ID: 8689482
[TBL] [Abstract][Full Text] [Related]
38. Histopathologic and immunocytochemical analysis of the retina and ocular tissues in Batten disease.
Bensaoula T; Shibuya H; Katz ML; Smith JE; Johnson GS; John SK; Milam AH
Ophthalmology; 2000 Sep; 107(9):1746-53. PubMed ID: 10964839
[TBL] [Abstract][Full Text] [Related]
39. A dominantly inherited chorioretinal degeneration resembling sectoral retinitis pigmentosa.
Rayborn ME; Moorhead LC; Hollyfield JG
Ophthalmology; 1982 Dec; 89(12):1441-54. PubMed ID: 7162787
[TBL] [Abstract][Full Text] [Related]
40. [Corneoretinal dystrophy (Bietti)-- Long-term course of one patient over a period of 30 years, and interindividual variability of clinical and electrophysiological findings in two patients].
Jurklies B; Jurklies C; Schmidt U; Wessing A; Bornfeld N
Klin Monbl Augenheilkd; 2001 Aug; 218(8):562-9. PubMed ID: 11573158
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
