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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 3
2004 2
2005 2
2006 4
2007 1
2008 1
2010 1
2012 2
2013 1
2014 1
2016 2
2017 3
2018 2
2019 4
2020 3
2021 1
2022 1
2024 0

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29 results

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Page 1
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients.
Bonnet C, Riahi Z, Chantot-Bastaraud S, Smagghe L, Letexier M, Marcaillou C, Lefèvre GM, Hardelin JP, El-Amraoui A, Singh-Estivalet A, Mohand-Saïd S, Kohl S, Kurtenbach A, Sliesoraityte I, Zobor D, Gherbi S, Testa F, Simonelli F, Banfi S, Fakin A, Glavač D, Jarc-Vidmar M, Zupan A, Battelino S, Martorell Sampol L, Claveria MA, Catala Mora J, Dad S, Møller LB, Rodriguez Jorge J, Hawlina M, Auricchio A, Sahel JA, Marlin S, Zrenner E, Audo I, Petit C. Bonnet C, et al. Among authors: kurtenbach a. Eur J Hum Genet. 2016 Dec;24(12):1730-1738. doi: 10.1038/ejhg.2016.99. Epub 2016 Jul 27. Eur J Hum Genet. 2016. PMID: 27460420 Free PMC article.
Usher Syndrome and Color Vision.
Kurtenbach A, Hahn G, Kernstock C, Hipp S, Zobor D, Stingl K, Kohl S, Bonnet C, Mohand-Saïd S, Sliesoraityte I, Sahel JA, Audo I, Fakin A, Hawlina M, Testa F, Simonelli F, Petit C, Zrenner E. Kurtenbach A, et al. Curr Eye Res. 2018 Oct;43(10):1295-1301. doi: 10.1080/02713683.2018.1501804. Epub 2018 Jul 30. Curr Eye Res. 2018. PMID: 30012035
The Tuebingen Scotopic Threshold Test (TSTT).
Strasser T, Langrova H, Sundermeier S, Hillerkuss D, Stingl K, Durst W, Kurtenbach A, Zrenner E, Zobor D. Strasser T, et al. Among authors: kurtenbach a. IEEE J Biomed Health Inform. 2018 Mar;22(2):607-610. doi: 10.1109/JBHI.2017.2648891. Epub 2017 Jan 5. IEEE J Biomed Health Inform. 2018. PMID: 28103197
Ophthalmic and Genetic Features of Bardet Biedl Syndrome in a German Cohort.
Nasser F, Kohl S, Kurtenbach A, Kempf M, Biskup S, Zuleger T, Haack TB, Weisschuh N, Stingl K, Zrenner E. Nasser F, et al. Among authors: kurtenbach a. Genes (Basel). 2022 Jul 8;13(7):1218. doi: 10.3390/genes13071218. Genes (Basel). 2022. PMID: 35886001 Free PMC article.
Investigation of summation mechanisms in the pupillomotor system.
Skorkovská K, Wilhelm H, Lüdtke H, Wilhelm B, Kurtenbach A. Skorkovská K, et al. Among authors: kurtenbach a. Graefes Arch Clin Exp Ophthalmol. 2014 Jul;252(7):1155-60. doi: 10.1007/s00417-014-2677-4. Epub 2014 May 29. Graefes Arch Clin Exp Ophthalmol. 2014. PMID: 24872024
Full-field electroretinography, visual acuity and visual fields in Usher syndrome: a multicentre European study.
Stingl K, Kurtenbach A, Hahn G, Kernstock C, Hipp S, Zobor D, Kohl S, Bonnet C, Mohand-Saïd S, Audo I, Fakin A, Hawlina M, Testa F, Simonelli F, Petit C, Sahel JA, Zrenner E. Stingl K, et al. Among authors: kurtenbach a. Doc Ophthalmol. 2019 Oct;139(2):151-160. doi: 10.1007/s10633-019-09704-8. Epub 2019 Jul 2. Doc Ophthalmol. 2019. PMID: 31267413
Age-related changes in retinal functional topography.
Langrová H, Zrenner E, Kurtenbach A, Seeliger MW. Langrová H, et al. Among authors: kurtenbach a. Invest Ophthalmol Vis Sci. 2008 Nov;49(11):5024-32. doi: 10.1167/iovs.07-1309. Epub 2008 Jun 6. Invest Ophthalmol Vis Sci. 2008. PMID: 18539946
Characteristics of Retinitis Pigmentosa Associated with ADGRV1 and Comparison with USH2A in Patients from a Multicentric Usher Syndrome Study Treatrush.
Fakin A, Bonnet C, Kurtenbach A, Mohand-Said S, Zobor D, Stingl K, Testa F, Simonelli F, Sahel JA, Audo I, Zrenner E, Hawlina M, Petit C. Fakin A, et al. Among authors: kurtenbach a. Int J Mol Sci. 2021 Sep 26;22(19):10352. doi: 10.3390/ijms221910352. Int J Mol Sci. 2021. PMID: 34638692 Free PMC article.
29 results