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Quoted phrase not found in phrase index: "Undetectable light-adapted electroretinogram"
Page 1
Phenotypic and genotypic features of POC1B-associated cone dystrophy.
Alzahem TA, AlTheeb A, Ba-Abbad R. Alzahem TA, et al. Ophthalmic Genet. 2024 Feb;45(1):72-77. doi: 10.1080/13816810.2023.2204361. Epub 2023 May 29. Ophthalmic Genet. 2024. PMID: 37246743
Clinical data analyzed included multimodal retinal imaging and electroretinography of the affected individuals. Genetic analysis was done for all probands. ...Macular optical coherence tomography showed reduced reflectivity of the external limiting membrane, ellipsoid, and …
Clinical data analyzed included multimodal retinal imaging and electroretinography of the affected individuals. Genetic analysis was …
Clinical and Molecular Characterization of Achromatopsia Patients: A Longitudinal Study.
Brunetti-Pierri R, Karali M, Melillo P, Di Iorio V, De Benedictis A, Iaccarino G, Testa F, Banfi S, Simonelli F. Brunetti-Pierri R, et al. Int J Mol Sci. 2021 Feb 7;22(4):1681. doi: 10.3390/ijms22041681. Int J Mol Sci. 2021. PMID: 33562422 Free PMC article.
At baseline, the patients presented a reduced best corrected visual acuity (BCVA), reduced macular sensitivity (MS), normal dark-adapted electroretinogram (ERG) responses and undetectable or severely reduced light-adapted ERG. The longitudinal analysis …
At baseline, the patients presented a reduced best corrected visual acuity (BCVA), reduced macular sensitivity (MS), normal dark-adapted …
Long-term follow-up of a Chinese patient with KCNV2-retinopathy.
Lie H, Wang G, Liu X, Meng X, Long Y, Ren J, Yang L, Fujinami-Yokokawa Y, Kurihara T, Tsubota K, Fujinami K, Li S. Lie H, et al. Ophthalmic Genet. 2021 Apr;42(2):144-149. doi: 10.1080/13816810.2020.1861307. Epub 2020 Dec 29. Ophthalmic Genet. 2021. PMID: 33372566 Free article.
Purpose: To characterize and monitor the clinical and electrophysiological features of a Chinese patient with KCNV2 retinopathy.Methods: A 17-year-old Chinese male with the diagnosis of cone dystrophy with supernormal rod response (CDSRR) was followed-up for 5 years, with full op …
Purpose: To characterize and monitor the clinical and electrophysiological features of a Chinese patient with KCNV2 retinopathy.Methods: A 1 …
A patient diagnosed with Galloway-Mowat syndrome presenting with a rod-cone functional anomaly with electronegative dark-adapted ERGs.
Racine J, Golden R. Racine J, et al. Doc Ophthalmol. 2021 Aug;143(1):75-83. doi: 10.1007/s10633-021-09820-4. Epub 2021 Feb 6. Doc Ophthalmol. 2021. PMID: 33548032
Therefore, the purpose of this case report is to reveal abnormal retinal function (including light-adapted and dark-adapted retinal function) in a female patient diagnosed with GAMOS due to mutation of the WDR73 gene. ...ISCEV standard ERG revealed residual response …
Therefore, the purpose of this case report is to reveal abnormal retinal function (including light-adapted and dark-adapted re …