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Year Number of Results
2015 10
2016 5
2017 4
2018 3
2019 6
2020 9
2021 4
2022 4
2023 2
2024 1

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Page 1
Clinical Phenotype of PDE6B-Associated Retinitis Pigmentosa.
Kuehlewein L, Zobor D, Stingl K, Kempf M, Nasser F, Bernd A, Biskup S, Cremers FPM, Khan MI, Mazzola P, Schäferhoff K, Heinrich T, Haack TB, Wissinger B, Zrenner E, Weisschuh N, Kohl S. Kuehlewein L, et al. Int J Mol Sci. 2021 Feb 27;22(5):2374. doi: 10.3390/ijms22052374. Int J Mol Sci. 2021. PMID: 33673512 Free PMC article.
[Development and validation of novel clinical endpoints in intermediate age-related macular degeneration in MACUSTAR].
Terheyden JH, Finger RP, Schmitz-Valckenberg S, Agostini H, Dahlke C, Kuehlewein L, Lang GE, Pauleikhoff D, Wolf A, Boettger MK, Luhmann UFO, Asmus F, Holz FG; MACUSTAR-Konsortium. Terheyden JH, et al. Among authors: kuehlewein l. Ophthalmologe. 2019 Dec;116(12):1186-1193. doi: 10.1007/s00347-019-0907-1. Ophthalmologe. 2019. PMID: 31087116 Review. German.
Adaptive optics ophthalmoscopy in retinitis pigmentosa (RP): Typical patterns.
Kortuem FC, Kempf M, Kuehlewein L, Nasser F, Kortuem C, Paques M, Kohl S, Ueffing M, Wissinger B, Zrenner E, Stingl K. Kortuem FC, et al. Among authors: kuehlewein l. Acta Ophthalmol. 2022 Nov;100(7):e1539-e1540. doi: 10.1111/aos.15183. Epub 2022 May 25. Acta Ophthalmol. 2022. PMID: 35611574 Free PMC article. No abstract available.
Clinical Protocols for the Evaluation of Rod Function.
Stingl K, Stingl K, Nowomiejska K, Kuehlewein L, Kohl S, Kempf M, Strasser T, Jung R, Wilhelm B, Peters T, Kelbsch C, Bartz-Schmidt KU, Langrova H, Zrenner E. Stingl K, et al. Among authors: kuehlewein l. Ophthalmologica. 2021;244(5):396-407. doi: 10.1159/000510888. Epub 2020 Aug 17. Ophthalmologica. 2021. PMID: 32805733
FUNDUS ALBIPUNCTATUS ASSOCIATED WITH CONE DYSFUNCTION.
Kuehlewein L, Nasser F, Gloeckle N, Kohl S, Zrenner E. Kuehlewein L, et al. Retin Cases Brief Rep. 2017 Winter;11 Suppl 1:S73-S76. doi: 10.1097/ICB.0000000000000420. Retin Cases Brief Rep. 2017. PMID: 27627638
Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment.
Bahena P, Daftarian N, Maroofian R, Linares P, Villalobos D, Mirrahimi M, Rad A, Doll J, Hofrichter MAH, Koparir A, Röder T, Han S, Sabbaghi H, Ahmadieh H, Behboudi H, Villanueva-Mendoza C, Cortés-Gonzalez V, Zamora-Ortiz R, Kohl S, Kuehlewein L, Darvish H, Alehabib E, Arenas-Sordo ML, Suri F, Vona B, Haaf T. Bahena P, et al. Among authors: kuehlewein l. Hum Genet. 2022 Apr;141(3-4):785-803. doi: 10.1007/s00439-021-02303-1. Epub 2021 Jun 20. Hum Genet. 2022. PMID: 34148116 Free PMC article.
CHANGES IN RETINAL SENSITIVITY AFTER GENE THERAPY IN CHOROIDEREMIA.
Fischer MD, Ochakovski GA, Beier B, Seitz IP, Vaheb Y, Kortuem C, Reichel FFL, Kuehlewein L, Kahle NA, Peters T, Girach A, Zrenner E, Ueffing M, MacLaren RE, Bartz-Schmidt K, Wilhelm B. Fischer MD, et al. Among authors: kuehlewein l. Retina. 2020 Jan;40(1):160-168. doi: 10.1097/IAE.0000000000002360. Retina. 2020. PMID: 30308560 Clinical Trial.
42 results