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Number of items: 13.

Seiler, R; Gunzinger, J M; Rüschoff, J H; Barthelmes, D; Bode, P K; Gerth-Kahlert, C (2018). Ungewöhnlicher kongenitaler Irisbefund. Der Ophthalmologe, 115(3):235-238.

Sturm, V; Gerth-Kahlert, C; Schworm, H D (2016). Komplexe Augenmuskelchirurgie. Der Augenspiegel, 09:46-49.

Gerth-Kahlert, C; Landau, K (2016). Wie viel Genetik steckt im Strabismus? Ars Medici, 22:1044-1046.

Chappaz, A; Knirsch, U; Gerth-Kahlert, C (2015). Alternating IV nerve palsy and ptosis as a first sign of childhood ocular myasthenia gravis. Pediatric Neurology, 52(4):460-461.

Tarnutzer, A A; Gerth-Kahlert, C; Timmann, D; Chang, D I; Harmuth, F; Bauer, P; Straumann, D; Synofzik, M (2015). Boucher-Neuhäuser syndrome: cerebellar degeneration, chorioretinal dystrophy and hypogonadotropic hypogonadism: two novel cases and a review of 40 cases from the literature. Journal of Neurology, 262(1):194-202.

Gerth-Kahlert, C; Seebauer, B; Dold, S; Hanson, J V M; Wildberger, H; Spörri, A; van Waes, H; Berger, W (2015). Intra-familial phenotype variability in patients with Jalili syndrome. Eye, 29(5):712-716.

Gerth-Kahlert, C; Michels, R; Funk, J; Gautschy, U (2014). Congenital Lamellar Cataract. JAMA Ophthalmology, 132(9):1122.

Vadasz, V; Fehr, J; Gerth-Kahlert, C (2014). Gelbe Flecken und wie weiter? Der Ophthalmologe, 111(12):1213-1216.

Gerth-Kahlert, C; Williamson, K; Ansari, M; Rainger, J K; Hingst, V; Zimmermann, T; Tech, S; Guthoff, R F; van Heyningen, V; FitzPatrick, D R (2013). Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single center. Molecular Genetics & Genomic Medicine, 1(1):15-31.

Gerth-Kahlert, C; Wildberger, H (2013). Optic disc doubling or pseudo-optic disc in colobomatous retinal abnormality? Journal of Neuro-Ophthalmology, 33(4):413.

Gerth-Kahlert, C. Phenotype characterization in macular dystrophies: The role of multifocal electroretinography and high-resolution optical coherence tomography. 2012, University of Zurich, Faculty of Medicine.

Gerth-Kahlert, C; Grisanti, S; Berger, E; Höhn, R; Witt, G; Jung, U (2011). Bilateral vitreous hemorrhage in a newborn with Stickler syndrome associated with a novel COL2A1 mutation. Journal of AAPOS, 15(3):311-313.

Gerth-Kahlert, C; Wermund, T K (2011). Optic neuritis. Klinische Monatsblätter für Augenheilkunde, 228(5):425-431.

This list was generated on Fri Nov 16 23:06:25 2018 CET.