Agnes B Renner
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Explore the profile of Agnes B Renner including associated specialties, affiliations and a list of published articles.
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26
Citations
708
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Recent Articles
1.
Solaki M, Baumann B, Reuter P, Andreasson S, Audo I, Ayuso C, et al.
Hum Mutat
. 2022 Mar;
43(7):832-858.
PMID: 35332618
Achromatopsia (ACHM) is a congenital cone photoreceptor disorder characterized by impaired color discrimination, low visual acuity, photosensitivity, and nystagmus. To date, six genes have been associated with ACHM (CNGA3, CNGB3,...
2.
Hufendiek K, Hufendiek K, Jagle H, Stohr H, Book M, Spital G, et al.
Int J Mol Sci
. 2020 Dec;
21(24).
PMID: 33302512
Autosomal recessive bestrophinopathy (ARB) has been reported as clinically heterogeneous. Eighteen patients (mean age: 22.5 years; 15 unrelated families) underwent ophthalmological examination, fundus photography, fundus autofluorescence, and optical coherence tomography...
3.
Plank T, Frolo J, Brandl-Ruhle S, Renner A, Jagle H, Greenlee M
Optom Vis Sci
. 2017 Jan;
94(3):297-310.
PMID: 28099241
Purpose: In patients with central visual field scotomata, a large part of visual cortex is not adequately stimulated. Patients often use a new eccentric fixation area on intact peripheral retina...
4.
Renner A, Dietrich-Ntoukas T, Jagle H
Doc Ophthalmol
. 2015 Oct;
131(3):221-30.
PMID: 26507840
Purpose: To describe clinical characteristics in a patient with recurrent episodes of night blindness due to vitamin A deficiency caused by short bowel syndrome in Crohn disease. Methods: Retrospective analysis...
5.
Renner A, Radeck V, Kellner U, Jagle H, Helbig H
Doc Ophthalmol
. 2014 Oct;
129(3):191-202.
PMID: 25300407
Purpose: To describe clinical characteristics of Müller cell sheen dystrophy (MCSD) in two unrelated patients followed for 10 years. Methods: Best-corrected visual acuity (BCVA), kinetic perimetry, biomicroscopy, ophthalmoscopy, fundus photography,...
6.
Renner A, Walter A, Fiebig B, Jagle H
Doc Ophthalmol
. 2012 Jun;
125(1):81-9.
PMID: 22674428
We report the clinical and genetic data obtained at a 17-year follow-up examination of a patient with gyrate atrophy, without an arginine-restricted diet. Patient examinations included visual acuity (VA), perimetry,...
7.
Plank T, Frolo J, Farzana F, Brandl-Ruhle S, Renner A, Greenlee M
Hum Brain Mapp
. 2012 Apr;
34(10):2607-23.
PMID: 22505353
In patients with central visual field scotomata a large part of visual cortex is not adequately stimulated. We investigated evidence for possible upregulation in cortical responses in 22 patients (8...
8.
Leng T, Marmor M, Kellner U, Thompson D, Renner A, Moore W, et al.
Retina
. 2012 Apr;
32(7):1411-9.
PMID: 22466470
Purpose: To describe a distinctive foveal cavitation as seen by spectral-domain optical coherence tomography in certain cone dysfunction syndromes. Methods: Observational case series. Patients were evaluated by dilated fundus examination,...
9.
Fritsche L, Fleckenstein M, Fiebig B, Schmitz-Valckenberg S, Bindewald-Wittich A, N Keilhauer C, et al.
Invest Ophthalmol Vis Sci
. 2012 Mar;
53(4):2112-8.
PMID: 22427542
Purpose. Age-related macular degeneration (AMD) is a heterogeneous condition of high prevalence and complex etiology involving genetic as well as environmental factors. By fundus autofluorescence (FAF) imaging, AMD can be...
10.
Audo I, Bujakowska K, Orhan E, Poloschek C, Defoort-Dhellemmes S, Drumare I, et al.
Am J Hum Genet
. 2012 Feb;
90(2):321-30.
PMID: 22325361
Congenital stationary night blindness (CSNB) is a heterogeneous retinal disorder characterized by visual impairment under low light conditions. This disorder is due to a signal transmission defect from rod photoreceptors...