163 related articles for article (PubMed ID: 32874040)
1. Electronegative Electroretinograms in the United Arab Emirates.
Alsalamah AK; Khan AO
Middle East Afr J Ophthalmol; 2020; 27(2):86-90. PubMed ID: 32874040
[TBL] [Abstract][Full Text] [Related]
2. Dysfunction of transmission in the inner retina: incidence and clinical causes of negative electroretinogram.
Renner AB; Kellner U; Cropp E; Foerster MH
Graefes Arch Clin Exp Ophthalmol; 2006 Nov; 244(11):1467-73. PubMed ID: 16612636
[TBL] [Abstract][Full Text] [Related]
3. Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy.
Hayashi T; Hosono K; Kurata K; Katagiri S; Mizobuchi K; Ueno S; Kondo M; Nakano T; Hotta Y
Doc Ophthalmol; 2020 Apr; 140(2):147-157. PubMed ID: 31583501
[TBL] [Abstract][Full Text] [Related]
4. Negative electroretinograms in the pediatric and adult population.
Kim JM; Payne JF; Yan J; Barnes CS
Doc Ophthalmol; 2012 Feb; 124(1):41-8. PubMed ID: 22246197
[TBL] [Abstract][Full Text] [Related]
5. Differentiation of murine models of "negative ERG" by single and repetitive light stimuli.
Tanimoto N; Akula JD; Fulton AB; Weber BH; Seeliger MW
Doc Ophthalmol; 2016 Apr; 132(2):101-9. PubMed ID: 26996188
[TBL] [Abstract][Full Text] [Related]
6. Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic association.
Marmor MF; Zeitz C
Doc Ophthalmol; 2018 Aug; 137(1):57-62. PubMed ID: 30051303
[TBL] [Abstract][Full Text] [Related]
7. Phenotypic characterization of complete CSNB in the inbred research beagle: how common is CSNB in research and companion dogs?
Oh A; Loew ER; Foster ML; Davidson MG; English RV; Gervais KJ; Herring IP; Mowat FM
Doc Ophthalmol; 2018 Oct; 137(2):87-101. PubMed ID: 30051304
[TBL] [Abstract][Full Text] [Related]
8. Genotype and phenotype of 101 dutch patients with congenital stationary night blindness.
Bijveld MM; Florijn RJ; Bergen AA; van den Born LI; Kamermans M; Prick L; Riemslag FC; van Schooneveld MJ; Kappers AM; van Genderen MM
Ophthalmology; 2013 Oct; 120(10):2072-81. PubMed ID: 23714322
[TBL] [Abstract][Full Text] [Related]
9. Long-term follow-up of retinal function and structure in
Al-Hujaili H; Taskintuna I; Neuhaus C; Bergmann C; Schatz P
Mol Vis; 2019; 25():851-858. PubMed ID: 31908403
[TBL] [Abstract][Full Text] [Related]
10. In vivo electroretinographic differentiation of rod, short-wavelength and long/medium-wavelength cone responses in dogs using silent substitution stimuli.
Mowat FM; Wise E; Oh A; Foster ML; Kremers J
Exp Eye Res; 2019 Aug; 185():107673. PubMed ID: 31128103
[TBL] [Abstract][Full Text] [Related]
11. Electroretinographic findings in a patient with congenital stationary night blindness due to a novel NYX mutation.
McAnany JJ; Alexander KR; Kumar NM; Ying H; Anastasakis A; Fishman GA
Ophthalmic Genet; 2013 Sep; 34(3):167-73. PubMed ID: 23289809
[TBL] [Abstract][Full Text] [Related]
12. Complete congenital stationary night blindness associated with a novel
Hayashi T; Murakami Y; Mizobuchi K; Koyanagi Y; Sonoda KH; Nakano T
Ophthalmic Genet; 2021 Aug; 42(4):412-419. PubMed ID: 33769208
[TBL] [Abstract][Full Text] [Related]
13. A phenotype-genotype correlation study of X-linked retinoschisis.
Vincent A; Robson AG; Neveu MM; Wright GA; Moore AT; Webster AR; Holder GE
Ophthalmology; 2013 Jul; 120(7):1454-64. PubMed ID: 23453514
[TBL] [Abstract][Full Text] [Related]
14. ISCEV extended protocol for the stimulus-response series for light-adapted full-field ERG.
McCulloch DL; Kondo M; Hamilton R; Lachapelle P; Messias AMV; Robson AG; Ueno S
Doc Ophthalmol; 2019 Jun; 138(3):205-215. PubMed ID: 30929108
[TBL] [Abstract][Full Text] [Related]
15. Congenital stationary night blindness: an update and review of the disease spectrum in Saudi Arabia.
Almutairi F; Almeshari N; Ahmad K; Magliyah MS; Schatz P
Acta Ophthalmol; 2021 Sep; 99(6):581-591. PubMed ID: 33369259
[TBL] [Abstract][Full Text] [Related]
16. Molecular profiling of complete congenital stationary night blindness: a pilot study on an Indian cohort.
Malaichamy S; Sen P; Sachidanandam R; Arokiasamy T; Lancelot ME; Audo I; Zeitz C; Soumittra N
Mol Vis; 2014; 20():341-51. PubMed ID: 24715752
[TBL] [Abstract][Full Text] [Related]
17. Extracting the ON and OFF contributions to the full-field photopic flash electroretinogram using summed growth curves.
Akula JD; Ambrosio L; Howard FI; Hansen RM; Fulton AB
Exp Eye Res; 2019 Dec; 189():107827. PubMed ID: 31600486
[TBL] [Abstract][Full Text] [Related]
18. Retinal findings in a patient of French ancestry with CABP4-related retinal disease.
Smirnov VM; Zeitz C; Soumittra N; Audo I; Defoort-Dhellemmes S
Doc Ophthalmol; 2018 Apr; 136(2):135-143. PubMed ID: 29525873
[TBL] [Abstract][Full Text] [Related]
19. RS-1 Gene Delivery to an Adult Rs1h Knockout Mouse Model Restores ERG b-Wave with Reversal of the Electronegative Waveform of X-Linked Retinoschisis.
Zeng Y; Takada Y; Kjellstrom S; Hiriyanna K; Tanikawa A; Wawrousek E; Smaoui N; Caruso R; Bush RA; Sieving PA
Invest Ophthalmol Vis Sci; 2004 Sep; 45(9):3279-85. PubMed ID: 15326152
[TBL] [Abstract][Full Text] [Related]
20. Electroretinography and optical coherence tomography reveal abnormal post-photoreceptoral activity and altered retinal lamination in patients with enhanced S-cone syndrome.
Sustar M; Perovšek D; Cima I; Stirn-Kranjc B; Hawlina M; Brecelj J
Doc Ophthalmol; 2015 Jun; 130(3):165-77. PubMed ID: 25663266
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]