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Felix Tonagel

University of Tübingen

34

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1105

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Dominant ACO2 mutations are a frequent cause of isolated optic atrophy

2021
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Pituitary apoplexy with macroadenoma

2021 Ophthalmologe
- Nawfel Ferrand
- Felix Tonagel
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Characteristics of peripapillary retinal nerve fiber layer atrophy in glaucoma, optic nerve sheath meningioma, and sphenoid wing meningioma.

2021 Graefes Archive for Clinical and Experimental Ophthalmology
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Mutation spectrum of the OPA1 gene in a large cohort of patients with suspected dominant optic atrophy: Identification and classification of 48 novel variants.

2021 PLOS ONE
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Leber’s hereditary optic neuropathy: course of disease in consideration of idebenone treatment and type of mutation

2020 Graefes Archive for Clinical and Experimental Ophthalmology
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Optic neuritis in German children: clinical findings and association with multiple sclerosis.

2020 Graefes Archive for Clinical and Experimental Ophthalmology
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First submicroscopic inversion of the OPA1 gene identified in dominant optic atrophy - a case report.

2020 BMC Medical Genetics
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Unilateral ocular malingering - a new test for the assessment of visual acuity

2019 Acta Ophthalmologica
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Visus und Gesichtsfeld bei Drusenpapillen

2019 Klinische Monatsblatter Fur Augenheilkunde
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Retrospective analysis of fractionated intensity-modulated radiotherapy (IMRT) in the interdisciplinary management of primary optic nerve sheath meningiomas

2019 Radiation Oncology
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