289 related articles for article (PubMed ID: 8190471)
1. Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy.
Sigesmund DA; Weleber RG; Pillers DA; Westall CA; Panton CM; Powell BR; Héon E; Murphey WH; Musarella MA; Ray PN
Ophthalmology; 1994 May; 101(5):856-65. PubMed ID: 8190471
[TBL] [Abstract][Full Text] [Related]
2. Ocular and neurodevelopmental features of Duchenne muscular dystrophy: a signature of dystrophin function in the central nervous system.
Ricotti V; Jägle H; Theodorou M; Moore AT; Muntoni F; Thompson DA
Eur J Hum Genet; 2016 Apr; 24(4):562-8. PubMed ID: 26081639
[TBL] [Abstract][Full Text] [Related]
3. Effects of dystrophin isoforms on signal transduction through neural retina: genotype-phenotype analysis of duchenne muscular dystrophy mouse mutants.
Pillers DA; Weleber RG; Green DG; Rash SM; Dally GY; Howard PL; Powers MR; Hood DC; Chapman VM; Ray PN; Woodward WR
Mol Genet Metab; 1999 Feb; 66(2):100-10. PubMed ID: 10068512
[TBL] [Abstract][Full Text] [Related]
4. [Correlation between electroretinographic findings, clinical phenotypic and genotypic analysis in Duchenne and Becker muscular dystrophy].
Yang Y; Zhang C; Sheng W; Pan S; Wu D; Jiang F
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Feb; 18(1):32-4. PubMed ID: 11172639
[TBL] [Abstract][Full Text] [Related]
5. mdxCv3 mouse is a model for electroretinography of Duchenne/Becker muscular dystrophy.
Pillers DA; Weleber RG; Woodward WR; Green DG; Chapman VM; Ray PN
Invest Ophthalmol Vis Sci; 1995 Feb; 36(2):462-6. PubMed ID: 7843915
[TBL] [Abstract][Full Text] [Related]
6. Asymmetrical Functional Deficits of ON and OFF Retinal Processing in the mdx3Cv Mouse Model of Duchenne Muscular Dystrophy.
Tsai TI; Barboni MT; Nagy BV; Roux MJ; Rendon A; Ventura DF; Kremers J
Invest Ophthalmol Vis Sci; 2016 Oct; 57(13):5788-5798. PubMed ID: 27792813
[TBL] [Abstract][Full Text] [Related]
7. Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutations.
Pillers DA; Fitzgerald KM; Duncan NM; Rash SM; White RA; Dwinnell SJ; Powell BR; Schnur RE; Ray PN; Cibis GW; Weleber RG
Hum Genet; 1999; 105(1-2):2-9. PubMed ID: 10480348
[TBL] [Abstract][Full Text] [Related]
8. The effects of dystrophin gene mutations on the ERG in mice and humans.
Cibis GW; Fitzgerald KM; Harris DJ; Rothberg PG; Rupani M
Invest Ophthalmol Vis Sci; 1993 Dec; 34(13):3646-52. PubMed ID: 8258524
[TBL] [Abstract][Full Text] [Related]
9. Electroretinogram in Duchenne/Becker muscular dystrophy.
Pascual Pascual SI; Molano J; Pascual-Castroviejo I
Pediatr Neurol; 1998 Apr; 18(4):315-20. PubMed ID: 9588526
[TBL] [Abstract][Full Text] [Related]
10. Retinal signal transmission in Duchenne muscular dystrophy: evidence for dysfunction in the photoreceptor/depolarizing bipolar cell pathway.
Fitzgerald KM; Cibis GW; Giambrone SA; Harris DJ
J Clin Invest; 1994 Jun; 93(6):2425-30. PubMed ID: 8200977
[TBL] [Abstract][Full Text] [Related]
11. Duchenne muscular dystrophy: negative electroretinograms and normal dark adaptation. Reappraisal of assignment of X linked incomplete congenital stationary night blindness.
Jensen H; Warburg M; Sjö O; Schwartz M
J Med Genet; 1995 May; 32(5):348-51. PubMed ID: 7616540
[TBL] [Abstract][Full Text] [Related]
12. Electroretinograms of eyes with Stickler syndrome.
Kondo H; Fujimoto K; Imagawa M; Oku K; Matsushita I; Hayashi T; Nagata T
Doc Ophthalmol; 2020 Jun; 140(3):233-243. PubMed ID: 31781920
[TBL] [Abstract][Full Text] [Related]
13. Dystrophin expression in the human retina is required for normal function as defined by electroretinography.
Pillers DA; Bulman DE; Weleber RG; Sigesmund DA; Musarella MA; Powell BR; Murphey WH; Westall C; Panton C; Becker LE
Nat Genet; 1993 May; 4(1):82-6. PubMed ID: 8513332
[TBL] [Abstract][Full Text] [Related]
14. ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy.
Fitzgerald KM; Cibis GW; Gettel AH; Rinaldi R; Harris DJ; White RA
J Med Genet; 1999 Apr; 36(4):316-22. PubMed ID: 10227401
[TBL] [Abstract][Full Text] [Related]
15. Duchenne muscular dystrophy: negative scotopic bright-flash electroretinogram but not congenital stationary night blindness.
Tremblay F; De Becker I; Dooley JM; Riddell DC
Can J Ophthalmol; 1994 Dec; 29(6):274-9. PubMed ID: 7834566
[TBL] [Abstract][Full Text] [Related]
16. Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.
Lines MA; Hébert M; McTaggart KE; Flynn SJ; Tennant MT; MacDonald IM
Ophthalmology; 2002 Oct; 109(10):1862-70. PubMed ID: 12359607
[TBL] [Abstract][Full Text] [Related]
17. RDH5 gene mutations and electroretinogram in fundus albipunctatus with or without macular dystrophy: RDH5 mutations and ERG in fundus albipunctatus.
Nakamura M; Skalet J; Miyake Y
Doc Ophthalmol; 2003 Jul; 107(1):3-11. PubMed ID: 12906118
[TBL] [Abstract][Full Text] [Related]
18. Duchenne muscular dystrophy: negative scotopic bright-flash electroretinogram and normal dark adaptation.
Tremblay F; De Becker I; Riddell DC; Dooley JM
Can J Ophthalmol; 1994 Dec; 29(6):280-3. PubMed ID: 7834567
[TBL] [Abstract][Full Text] [Related]
19. Altered visual processing in the mdx52 mouse model of Duchenne muscular dystrophy.
Barboni MTS; Liber AMP; Joachimsthaler A; Saoudi A; Goyenvalle A; Rendon A; Roger JE; Ventura DF; Kremers J; Vaillend C
Neurobiol Dis; 2021 May; 152():105288. PubMed ID: 33556541
[TBL] [Abstract][Full Text] [Related]
20. Electroretinogram in cone dystrophy.
Iijima H; Yamaguchi S; Kogure S; Hosaka O; Shibutani T
Jpn J Ophthalmol; 1991; 35(4):453-66. PubMed ID: 1821435
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
