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Year Number of Results
2011 2
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Page 1
[Ciliopathies].
Gerth-Kahlert C, Koller S. Gerth-Kahlert C, et al. Klin Monbl Augenheilkd. 2018 Mar;235(3):264-272. doi: 10.1055/a-0573-9199. Epub 2018 Mar 13. Klin Monbl Augenheilkd. 2018. PMID: 29534263 Review. German.
Retinal Function in Advanced Multiple Sclerosis.
Hanson JVM, Single S, Eberle RB, Kana V, Ineichen BV, Gerth-Kahlert C. Hanson JVM, et al. Among authors: gerth kahlert c. Invest Ophthalmol Vis Sci. 2024 Nov 4;65(13):2. doi: 10.1167/iovs.65.13.2. Invest Ophthalmol Vis Sci. 2024. PMID: 39495184 Free PMC article.
Congenital lamellar cataract.
Gerth-Kahlert C, Michels R, Funk J, Gautschy U. Gerth-Kahlert C, et al. JAMA Ophthalmol. 2014 Sep;132(9):1122. doi: 10.1001/jamaophthalmol.2013.5851. JAMA Ophthalmol. 2014. PMID: 25032728 No abstract available.
Variants in CFAP410 cause a range of retinal and skeletal phenotypes.
Schmidt RE, Pohodich AE, Birch D, Jones K, Lam BL, Jung EH, Jain N, Georgiou M, Mahroo OA, Webster AR, Michaelides M, Bakall B, Iannaccone A, Vincent A, Parameswarappa DC, Heon E, Scholl HPN, Janeschitz-Kriegl L, Traboulsi EI, Zein W, Brooks BP, Cukras C, Hufnagel R, Aleman TS, Sylla MM, Tsang SH, Alabek M, Sahel J, Gorin MB, van Genderen MM, Stingl K, Reith M, Kohl S, Amaral RAS, Sallum JMF, Vincent AL, Hull S, Duncan JL, Hanson JVM, Tedeus M, Maggi J, Graf U, Koller S, Berger W, Gerth-Kahlert C, Marra M, Everett LA, Yang P, Pennesi ME. Schmidt RE, et al. Among authors: gerth kahlert c. NPJ Genom Med. 2025 Apr 17;10(1):32. doi: 10.1038/s41525-025-00489-1. NPJ Genom Med. 2025. PMID: 40246852 Free PMC article.
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders.
Jurgens JA, Barry BJ, Chan WM, MacKinnon S, Whitman MC, Matos Ruiz PM, Pratt BM, England EM, Pais L, Lemire G, Groopman E, Glaze C, Russell KA, Singer-Berk M, Di Gioia SA, Lee AS, Andrews C, Shaaban S, Wirth MM, Bekele S, Toffoloni M, Bradford VR, Foster EE, Berube L, Rivera-Quiles C, Mensching FM, Sanchis-Juan A, Fu JM, Wong I, Zhao X, Wilson MW, Weisburd B, Lek M; Ocular CCDD Phenotyping Consortium; Brand H, Talkowski ME, MacArthur DG, O'Donnell-Luria A, Robson CD, Hunter DG, Engle EC. Jurgens JA, et al. Genet Med. 2025 Apr;27(4):101216. doi: 10.1016/j.gim.2024.101216. Epub 2024 Jul 18. Genet Med. 2025. PMID: 39033378 Free PMC article.
[Optic neuritis].
Gerth-Kahlert C, Wermund TK. Gerth-Kahlert C, et al. Klin Monbl Augenheilkd. 2011 May;228(5):425-31. doi: 10.1055/s-0029-1246038. Epub 2011 Mar 11. Klin Monbl Augenheilkd. 2011. PMID: 21400403 Review. German.
Flicker electroretinogram in newborn infants.
Hanson JVM, Weber C, Pfäffli OA, Bassler D, McCulloch DL, Gerth-Kahlert C. Hanson JVM, et al. Among authors: gerth kahlert c. Doc Ophthalmol. 2022 Dec;145(3):175-184. doi: 10.1007/s10633-022-09889-5. Epub 2022 Oct 6. Doc Ophthalmol. 2022. PMID: 36199003 Free PMC article.
[Unusual congenital iris finding].
Seiler R, Gunzinger JM, Rüschoff JH, Barthelmes D, Bode PK, Gerth-Kahlert C. Seiler R, et al. Among authors: gerth kahlert c. Ophthalmologe. 2018 Mar;115(3):235-238. doi: 10.1007/s00347-017-0530-y. Ophthalmologe. 2018. PMID: 28656332 German. No abstract available.
Flicker electroretinogram in preterm infants.
Taner AF, Hanson JVM, Weber C, Bassler D, McCulloch DL, Gerth-Kahlert C. Taner AF, et al. Among authors: gerth kahlert c. Eye (Lond). 2024 Oct;38(14):2768-2774. doi: 10.1038/s41433-024-03127-9. Epub 2024 May 23. Eye (Lond). 2024. PMID: 38783086 Free PMC article.
78 results