Maintenance Infos

Browse by Creators

Navigate back| Up a level
Export as
Number of items: 26.

Zweipfenning, Florian; Toelle, Sandra P; Gerth-Kahlert, Christina (2019). Tuberöse-Sklerose-Komplex: Analyse des okulären Phänotyps und assoziierter Komplikationen. Klinische Monatsblätter für Augenheilkunde, 236(04):462-468.

Gerull, Roland; Brauer, Viviane; Bassler, Dirk; Laubscher, Bernard; Pfister, Riccardo E; Nelle, Mathias; Müller, Beatrice; Roth-Kleiner, Matthias; Gerth-Kahlert, Christina; Adams, Mark; Swiss Neonatal Network; Follow-up Group (2018). Prediction of ROP Treatment and Evaluation of Screening Criteria in VLBW Infants-a Population Based Analysis. Pediatric Research, 84(5):632-638.

Gerth-Kahlert, Christina; Koller, Samuel (2018). Retinale Ziliopathien. Klinische Monatsblätter für Augenheilkunde, 235(3):264-272.

Hanson, James V M; Hediger, Michael; Manogaran, Praveena; Landau, Klara; Hagenbuch, Niels; Schippling, Sven; Gerth-Kahlert, Christina (2018). Outer Retinal Dysfunction in the Absence of Structural Abnormalities in Multiple Sclerosis. Investigative Ophthalmology & Visual Science [IOVS], 59(1):549-560.

Gerth-Kahlert, Christina; Maggi, Jordi; Töteberg-Harms, Marc; Tiwari, Amit; Budde, Birgit; Nürnberg, Peter; Koller, Samuel; Berger, Wolfgang (2018). Absence of Goniodysgenesis in Patients with Chromosome 13Q Microdeletion-Related Microcoria. Ophthalmology Glaucoma, 1(2):145-147.

Gerull, Roland; Brauer, Viviane; Bassler, Dirk; Laubscher, Bernard; Pfister, Riccardo E; Nelle, Mathias; Müller, Béatrice; Gerth-Kahlert, Christina; Adams, Mark; Swiss Neonatal Network; Follow-up Group (2018). Incidence of retinopathy of prematurity (ROP) and ROP treatment in Switzerland 2006-2015: a population-based analysis. Archives of Disease in Childhood. Fetal and Neonatal Edition, 103(4):F337-F342.

Ambroz, S C; Töteberg-Harms, M; Hanson, James V M; Funk, J; Barthelmes, D; Gerth-Kahlert, Christina (2018). Outcome of Pediatric Cataract Surgeries in a Tertiary Center in Switzerland. Journal of Ophthalmology:3230489.

Zehnder, Simon; Wildberger, Hannes; Hanson, James V M; Lukas, Sebastian; Pelz, Stefan; Landau, Klara; Wichmann, Werner; Gerth-Kahlert, Christina (2018). Retinal ganglion cell topography in patients with visual pathway pathology. Journal of Neuro-Ophthalmology, 38(2):172-178.

Lin, Ting-Feng; Gerth-Kahlert, Christina; Hanson, James V M; Straumann, Dominik; Huang, Melody Ying-Yu (2018). Spontaneous Nystagmus in the Dark in an Infantile Nystagmus Patient May Represent Negative Optokinetic Afternystagmus. Frontiers in Neurology, 9:151.

Gerth-Kahlert, Christina; Tiwari, Amit; Hauri-Hohl, Mathias M; Hanson, James V M; Bahr, Angela; Palmowski-Wolfe, Anja; Güngör, Tayfun; Berger, Wolfgang (2018). Unusual retinopathy in a child with severe combined immune deficiency. Ophthalmic Genetics, 39(1):92-94.

Hackenberg, Annette; Boltshauser, Eugen; Gerth-Kahlert, Christina; Stahr, Nikolai; Azzarello-Burri, Silvia; Plecko, Barbara (2017). Horizontal gaze palsy in two brothers with compound heterozygous ROBO3 gene mutations. Neuropediatrics, 48(01):57-58.

Theiler, Martin; Baselga, Eulalia; Gerth-Kahlert, Christina; Mathes, Erin F; Schwieger-Briel, Agnes; Chaloupka, Karla; Weibel, Lisa; Frieden, Ilona J (2017). Infantile hemangiomas with conjunctival involvement: an underreported occurrence. Pediatric Dermatology, 34(6):681-685.

Gerth-Kahlert, Christina; Tiwari, Amit; Hanson, James V M; Batmanabane, Vaishnavi; Traboulsi, Elias; Pennesi, Mark E; Al-Qahtani, Abdullah A; Lam, Byron L; Heckenlively, John; Zweifel, Sandrine A; Vincent, Ajoy; Fierz, Fabienne; Barthelmes, Daniel; Branham, Kari; Khan, Naheed; Bahr, Angela; Baehr, Luzy; Magyar, István; Koller, Samuel; Azzarello-Burri, Silvia; Niedrist, Dunja; Heon, Elise; Berger, Wolfgang (2017). C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations. Investigative Ophthalmology & Visual Science [IOVS], 58(10):3840-3850.

Bolognini, Ramona; Gerth-Kahlert, Christina; Abegg, Mathias; Bartholdi, Deborah; Mathis, Nicolas; Sturm, Veit; Gallati, Sabina; Schaller, André (2017). Characterization of two novel intronic OPA1 mutations resulting in aberrant pre-mRNA splicing. BMC Medical Genetics, 18(1):22.

Panorgias, Athanasios; Tillman, Megan; Sutter, Erich E; Moshiri, Ala; Gerth-Kahlert, Christina; Werner, John S (2017). Senescent Changes and Topography of the Dark-Adapted Multifocal Electroretinogram. Investigative Ophthalmology & Visual Science [IOVS], 58(2):1323-1329.

Richardson, Rose; Sowden, Jane; Gerth-Kahlert, Christina; Moore, Anthony T; Moosajee, Mariya (2017). Clinical utility gene card for: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches. European Journal of Human Genetics, 25:e1-e6.

Fierz, Fabienne C; Gerth-Kahlert, Christina (2017). Long-Term Follow-Up in Children with Anisocoria: Cocaine Test Results and Patient Outcome. Journal of Ophthalmology:7575040.

Manogaran, Praveena; Hanson, James V M; Olbert, Elisabeth D; Egger, Christine; Wicki, Carla; Gerth-Kahlert, Christina; Landau, Klara; Schippling, Sven (2016). Optical Coherence Tomography and Magnetic Resonance Imaging in Multiple Sclerosis and Neuromyelitis Optica Spectrum Disorder. International Journal of Molecular Sciences, 17(11):1-13.

Chappaz, Ariane; Barthelmes, Daniel; Buser, Lorenz; Funk, Jens; Gerth-Kahlert, Christina (2016). Iris cyst in a child with Aicardi syndrome: a novel association. Journal of AAPOS, 20(5):451-452.

Kana, Veronika; Petersen, Jens A; Ikenberg, Kristian; Chappaz, Ariane; Gerth-Kahlert, Christina; Appenzeller, Philippe; Linnebank, Michael (2016). Teaching NeuroImages: Recurrent oculomotor palsies caused by neurosarcoidosis. Neurology, 87(3):e31-e32.

Liu, Chunqiao; Widen, Sonya A; Williamson, Kathleen A; Ratnapriya, Rinki; Gerth-Kahlert, Christina; Rainger, Joe; Alur, Ramakrishna P; Strachan, Erin; Manjunath, Souparnika H; Balakrishnan, Archana; Floyd, James A; Li, Tiansen; Waskiewicz, Andrew; Brooks, Brian P; Lehmann, Ordan J; FitzPatrick, David R; Swaroop, Anand (2016). A secreted WNT-ligand-binding domain of FZD5 generated by a frameshift mutation causes autosomal dominant coloboma. Human Molecular Genetics, 25(7):1382-1391.

Hanson, James V M; Sromicki, Julian; Mangold, Mario; Golling, Matthias; Gerth-Kahlert, Christina (2016). Maculopathy following exposure to visible and infrared radiation from a laser pointer: a clinical case study. Documenta ophthalmologica. Advances in ophthalmology, 132(2):147-155.

Vincent, Ajoy; Ng, Judith; Gerth-Kahlert, Christina; Tavares, Erika; Maynes, Jason T; Wright, Thomas; Tiwari, Amit; Tumber, Anupreet; Li, Shuning; Hanson, James V M; Bahr, Angela; MacDonald, Heather; Bähr, Luzy; Westall, Carol; Berger, Wolfgang; Cremers, Frans P M; den Hollander, Anneke I; Héon, Elise (2016). Biallelic mutations in CRB1 underlie autosomal recessive familial foveal retinoschisis. Investigative Ophthalmology & Visual Science [IOVS], 57:2637-2646.

Tiwari, Amit; Bahr, Angela; Bähr, Luzy; Fleischhauer, Johannes; Zinkernagel, Martin S; Winkler, Niklas; Barthelmes, Daniel; Berger, Lieselotte; Gerth-Kahlert, Christina; Neidhardt, John; Berger, Wolfgang (2016). Next generation sequencing based identification of disease-associated mutations in Swiss patients with retinal dystrophies. Scientific Reports, 6:28755.

Vadasz, Vinzenz A C; Gerth-Kahlert, Christina (2015). The Lemierre syndrome - a neuroophthalmological approach. Utah: Spencer S. Eccles Health Sciences Library, University of Utah.

Luder, Hans U; Gerth-Kahlert, Christina; Ostertag-Benzinger, Silke; Schorderet, Daniel F (2013). Dental phenotype in Jalili Syndrome due to a c.1312 dupC homozygous mutation in the CNNM4 gene. PLoS ONE, 8(10):e78529.

This list was generated on Wed Jun 19 11:11:02 2019 CEST.