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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. Among authors: hanson jvm. Acta Ophthalmol. 2021 Jun;99(4):e594-e607. doi: 10.1111/aos.14615. Epub 2020 Sep 30. Acta Ophthalmol. 2021. PMID: 32996714 Free article.
Intra-familial phenotype variability in patients with Jalili syndrome.
Gerth-Kahlert C, Seebauer B, Dold S, Hanson JV, Wildberger H, Spörri A, van Waes H, Berger W. Gerth-Kahlert C, et al. Eye (Lond). 2015 May;29(5):712-6. doi: 10.1038/eye.2014.314. Epub 2015 Jan 23. Eye (Lond). 2015. PMID: 25613845 Free PMC article. No abstract available.
Biallelic Mutations in CRB1 Underlie Autosomal Recessive Familial Foveal Retinoschisis.
Vincent A, Ng J, Gerth-Kahlert C, Tavares E, Maynes JT, Wright T, Tiwari A, Tumber A, Li S, Hanson JV, Bahr A, MacDonald H, Bähr L, Westall C, Berger W, Cremers FP, den Hollander AI, Héon E. Vincent A, et al. Invest Ophthalmol Vis Sci. 2016 May 1;57(6):2637-46. doi: 10.1167/iovs.15-18281. Invest Ophthalmol Vis Sci. 2016. PMID: 27258436 Free article.
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. Among authors: hanson jvm. 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.
Unusual retinopathy in a child with severe combined immune deficiency.
Gerth-Kahlert C, Tiwari A, Hauri-Hohl MM, Hanson JVM, Bahr A, Palmowski-Wolfe A, Güngör T, Berger W. Gerth-Kahlert C, et al. Among authors: hanson jvm. Ophthalmic Genet. 2018 Jan-Feb;39(1):92-94. doi: 10.1080/13816810.2017.1350721. Epub 2017 Aug 16. Ophthalmic Genet. 2018. PMID: 28812413
Retinal Ganglion Cell Topography in Patients With Visual Pathway Pathology.
Zehnder S, Wildberger H, Hanson JVM, Lukas S, Pelz S, Landau K, Wichmann W, Gerth-Kahlert C. Zehnder S, et al. Among authors: hanson jvm. J Neuroophthalmol. 2018 Jun;38(2):172-178. doi: 10.1097/WNO.0000000000000589. J Neuroophthalmol. 2018. PMID: 29210928 Free article.
36 results