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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.
[Unusual congenital iris finding].
Seiler R, Gunzinger JM, Rüschoff JH, Barthelmes D, Bode PK, Gerth-Kahlert C. Seiler R, et al. Ophthalmologe. 2018 Mar;115(3):235-238. doi: 10.1007/s00347-017-0530-y. Ophthalmologe. 2018. PMID: 28656332 German. No abstract available.
C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations.
Gerth-Kahlert C, Tiwari A, Hanson JVM, Batmanabane V, Traboulsi E, Pennesi ME, Al-Qahtani AA, Lam BL, Heckenlively J, Zweifel SA, Vincent A, Fierz F, Barthelmes D, Branham K, Khan N, Bahr A, Baehr L, Magyar I, Koller S, Azzarello-Burri S, Niedrist D, Heon E, Berger W. Gerth-Kahlert C, et al. Invest Ophthalmol Vis Sci. 2017 Aug 1;58(10):3840-3850. doi: 10.1167/iovs.17-21597. Invest Ophthalmol Vis Sci. 2017. PMID: 28763557 Free article.
Genotype-phenotype spectrum in isolated and syndromic nanophthalmos.
Lang E, Koller S, Atac D, Pfäffli OA, Hanson JVM, Feil S, Bähr L, Bahr A, Kottke R, Joset P, Fasler K, Barthelmes D, Steindl K, Konrad D, Wille DA, Berger W, Gerth-Kahlert C. Lang E, et al. Acta Ophthalmol. 2021 Jun;99(4):e594-e607. doi: 10.1111/aos.14615. Epub 2020 Sep 30. Acta Ophthalmol. 2021. PMID: 32996714 Free article.
Functional and Morphological Characteristics of the Retina of Patients with Drusen-like Deposits and Systemic Lupus Erythematosus Treated with Hydroxychloroquine: A Retrospective Study.
Kitay AM, Hanson JVM, Hasan N, Driban M, Chhablani J, Barthelmes D, Gerth-Kahlert C, Al-Sheikh M. Kitay AM, et al. Among authors: gerth kahlert c. Biomedicines. 2023 Jun 3;11(6):1629. doi: 10.3390/biomedicines11061629. Biomedicines. 2023. PMID: 37371724 Free PMC article.
63 results