318 related articles for article (PubMed ID: 2963026)
1. Neuro-ophthalmic presentation of cone dysfunction syndromes in the adult.
Zervas JP; Smith JL
J Clin Neuroophthalmol; 1987 Dec; 7(4):202-18. PubMed ID: 2963026
[TBL] [Abstract][Full Text] [Related]
2. Foveal cone dysfunction syndrome.
ten Hove MW; Siatkowski RM; Smith JL
J Neuroophthalmol; 1998 Mar; 18(1):9-14. PubMed ID: 9532531
[TBL] [Abstract][Full Text] [Related]
3. Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy.
Tyni T; Kivelä T; Lappi M; Summanen P; Nikoskelainen E; Pihko H
Ophthalmology; 1998 May; 105(5):810-24. PubMed ID: 9593380
[TBL] [Abstract][Full Text] [Related]
4. Cone dystrophies: clinical and electrophysiological findings.
Kellner U; Kleine-Hartlage P; Foerster MH
Ger J Ophthalmol; 1992; 1(2):105-9. PubMed ID: 1477624
[TBL] [Abstract][Full Text] [Related]
5. Mutation in the gene GUCA1A, encoding guanylate cyclase-activating protein 1, causes cone, cone-rod, and macular dystrophy.
Michaelides M; Wilkie SE; Jenkins S; Holder GE; Hunt DM; Moore AT; Webster AR
Ophthalmology; 2005 Aug; 112(8):1442-7. PubMed ID: 15953638
[TBL] [Abstract][Full Text] [Related]
6. Alström syndrome--a case report and literature review.
Karska-Basta I; Kubicka-Trzaska A; Filemonowicz-Skoczek A; Romanowska-Dixon B; Kobylarz J
Klin Oczna; 2008; 110(4-6):188-92. PubMed ID: 18655459
[TBL] [Abstract][Full Text] [Related]
7. A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1.
Michaelides M; Holder GE; Hunt DM; Fitzke FW; Bird AC; Moore AT
Br J Ophthalmol; 2005 Feb; 89(2):198-206. PubMed ID: 15665353
[TBL] [Abstract][Full Text] [Related]
8. Choroideremia: variability of clinical and electrophysiological characteristics and first report of a negative electroretinogram.
Renner AB; Kellner U; Cropp E; Preising MN; MacDonald IM; van den Hurk JA; Cremers FP; Foerster MH
Ophthalmology; 2006 Nov; 113(11):2066.e1-10. PubMed ID: 16935340
[TBL] [Abstract][Full Text] [Related]
9. Acute zonal occult outer retinopathy. Donders Lecture: The Netherlands Ophthalmological Society, Maastricht, Holland, June 19, 1992.
Gass JD
J Clin Neuroophthalmol; 1993 Jun; 13(2):79-97. PubMed ID: 8340485
[TBL] [Abstract][Full Text] [Related]
10. Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.
Wissinger B; Dangel S; Jägle H; Hansen L; Baumann B; Rudolph G; Wolf C; Bonin M; Koeppen K; Ladewig T; Kohl S; Zrenner E; Rosenberg T
Invest Ophthalmol Vis Sci; 2008 Feb; 49(2):751-7. PubMed ID: 18235024
[TBL] [Abstract][Full Text] [Related]
11. RP cone-rod degeneration.
Heckenlively JR
Trans Am Ophthalmol Soc; 1987; 85():438-70. PubMed ID: 3447340
[TBL] [Abstract][Full Text] [Related]
12. Peripheral cone dystrophy: a variant of cone dystrophy with predominant dysfunction in the peripheral cone system.
Kondo M; Miyake Y; Kondo N; Ueno S; Takakuwa H; Terasaki H
Ophthalmology; 2004 Apr; 111(4):732-9. PubMed ID: 15051206
[TBL] [Abstract][Full Text] [Related]
13. Restored photoreceptor outer segment damage in multiple evanescent white dot syndrome.
Li D; Kishi S
Ophthalmology; 2009 Apr; 116(4):762-70. PubMed ID: 19344825
[TBL] [Abstract][Full Text] [Related]
14. Neuro-ophthalmologic features of spinocerebellar ataxia type 7.
Miller RC; Tewari A; Miller JA; Garbern J; Van Stavern GP
J Neuroophthalmol; 2009 Sep; 29(3):180-6. PubMed ID: 19726938
[TBL] [Abstract][Full Text] [Related]
15. Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration.
Lewis CA; Batlle IR; Batlle KG; Banerjee P; Cideciyan AV; Huang J; Alemán TS; Huang Y; Ott J; Gilliam TC; Knowles JA; Jacobson SG
Invest Ophthalmol Vis Sci; 1999 Aug; 40(9):2106-14. PubMed ID: 10440267
[TBL] [Abstract][Full Text] [Related]
16. Novel mutations and electrophysiologic findings in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia).
Michaelides M; Li Z; Rana NA; Richardson EC; Hykin PG; Moore AT; Holder GE; Webster AR
Ophthalmology; 2010 Jan; 117(1):120-127.e1. PubMed ID: 19818506
[TBL] [Abstract][Full Text] [Related]
17. Macular dysfunction and morphology in spinocerebellar ataxia type 7 (SCA 7).
Hugosson T; Gränse L; Ponjavic V; Andréasson S
Ophthalmic Genet; 2009 Mar; 30(1):1-6. PubMed ID: 19172503
[TBL] [Abstract][Full Text] [Related]
18. Bull's-eye maculopathy and negative electroretinogram.
Miyake Y; Shiroyama N; Horiguchi M; Saito A; Yagasaki K
Retina; 1989; 9(3):210-5. PubMed ID: 2595114
[TBL] [Abstract][Full Text] [Related]
19. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.
Smith PR; Bain SC; Good PA; Hattersley AT; Barnett AH; Gibson JM; Dodson PM
Ophthalmology; 1999 Jun; 106(6):1101-8. PubMed ID: 10366077
[TBL] [Abstract][Full Text] [Related]
20. Fundus flavimaculatus with severely reduced cone electroretinogram.
Iijima H; Gohdo T; Hosaka O
Jpn J Ophthalmol; 1992; 36(3):249-56. PubMed ID: 1464966
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]