Gerth-Kahlert C - Search Results

1

The "Eyelet Sign" as an MRI Clue for Inflammatory Brown Syndrome.

Fierz FC, Landau K, Kottke R, Wichmann W, Sturm V, Weber KP, Gerth-Kahlert C. Fierz FC, et al. J Neuroophthalmol. 2022 Mar 1;42(1):115-120. doi: 10.1097/WNO.0000000000001237. Epub 2021 Apr 14. J Neuroophthalmol. 2022. PMID: 33870947

2

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. J Neuroophthalmol. 2018 Jun;38(2):172-178. doi: 10.1097/WNO.0000000000000589. J Neuroophthalmol. 2018. PMID: 29210928 Free article.

3

Long-Term Follow-Up in Children with Anisocoria: Cocaine Test Results and Patient Outcome.

Fierz FC, Gerth-Kahlert C. Fierz FC, et al. J Ophthalmol. 2017;2017:7575040. doi: 10.1155/2017/7575040. Epub 2017 Dec 4. J Ophthalmol. 2017. PMID: 29348932 Free PMC article.

4

Genetic Analysis in a Swiss Cohort of Bilateral Congenital Cataract.

Rechsteiner D, Issler L, Koller S, Lang E, Bähr L, Feil S, Rüegger CM, Kottke R, Toelle SP, Zweifel N, Steindl K, Joset P, Zweier M, Suter AA, Gogoll L, Haas C, Berger W, Gerth-Kahlert C. Rechsteiner D, et al. JAMA Ophthalmol. 2021 Jul 1;139(7):691-700. doi: 10.1001/jamaophthalmol.2021.0385. JAMA Ophthalmol. 2021. PMID: 34014271 Free PMC article.

5

Homozygosity for a Novel DOCK7 Variant Due to Segmental Uniparental Isodisomy of Chromosome 1 Associated with Early Infantile Epileptic Encephalopathy (EIEE) and Cortical Visual Impairment.

Kivrak Pfiffner F, Koller S, Ménétrey A, Graf U, Bähr L, Maspoli A, Hackenberg A, Kottke R, Gerth-Kahlert C, Berger W. Kivrak Pfiffner F, et al. Among authors: gerth kahlert c. Int J Mol Sci. 2022 Jul 2;23(13):7382. doi: 10.3390/ijms23137382. Int J Mol Sci. 2022. PMID: 35806387 Free PMC article.

6

Outer Retinal Dysfunction in the Absence of Structural Abnormalities in Multiple Sclerosis.

Hanson JVM, Hediger M, Manogaran P, Landau K, Hagenbuch N, Schippling S, Gerth-Kahlert C. Hanson JVM, et al. Invest Ophthalmol Vis Sci. 2018 Jan 1;59(1):549-560. doi: 10.1167/iovs.17-22821. Invest Ophthalmol Vis Sci. 2018. PMID: 29372253 Free article.

7

Outer Retinal Dysfunction in the Absence of Structural Abnormalities in Multiple Sclerosis.

Hanson JVM, Hediger M, Manogaran P, Landau K, Hagenbuch N, Schippling S, Gerth-Kahlert C. Hanson JVM, et al. Invest Ophthalmol Vis Sci. 2018 Jan 1;59(1):549-560. doi: 10.1167/iovs.17-22821. Invest Ophthalmol Vis Sci. 2018. PMID: 29372255 Free article.

8

Atonal homolog 7 (ATOH7) loss-of-function mutations in predominant bilateral optic nerve hypoplasia.

Atac D, Koller S, Hanson JVM, Feil S, Tiwari A, Bahr A, Baehr L, Magyar I, Kottke R, Gerth-Kahlert C, Berger W. Atac D, et al. Hum Mol Genet. 2020 Jan 1;29(1):132-148. doi: 10.1093/hmg/ddz268. Hum Mol Genet. 2020. PMID: 31696227 Free article.

9

Optical Coherence Tomography and Magnetic Resonance Imaging in Multiple Sclerosis and Neuromyelitis Optica Spectrum Disorder.

Manogaran P, Hanson JV, Olbert ED, Egger C, Wicki C, Gerth-Kahlert C, Landau K, Schippling S. Manogaran P, et al. Int J Mol Sci. 2016 Nov 15;17(11):1894. doi: 10.3390/ijms17111894. Int J Mol Sci. 2016. PMID: 27854301 Free PMC article. Review.

10

Characterization of two novel intronic OPA1 mutations resulting in aberrant pre-mRNA splicing.

Bolognini R, Gerth-Kahlert C, Abegg M, Bartholdi D, Mathis N, Sturm V, Gallati S, Schaller A. Bolognini R, et al. BMC Med Genet. 2017 Feb 28;18(1):22. doi: 10.1186/s12881-017-0383-x. BMC Med Genet. 2017. PMID: 28245802 Free PMC article.

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