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

por Fierz, Fabienne C., Gerth-Kahlert, Christina
Publicado 2017

Challenges in Patients with Trisomy 21: A Review of Current Knowledge and Recommendations

por Robinson, Jennifer, Pompe, Manca Tekavčič, Gerth-Kahlert, Christina
Publicado 2021

Commentary: Outer Retinal Dysfunction on Multifocal Electroretinography May Help Differentiating Multiple Sclerosis From Neuromyelitis Optica Spectrum Disorder

por Hanson, James V. M., Schippling, Sven, Gerth-Kahlert, Christina
Publicado 2020

Dental Phenotype in Jalili Syndrome Due to a c.1312 dupC Homozygous Mutation in the CNNM4 Gene

por Luder, Hans U., Gerth-Kahlert, Christina, Ostertag-Benzinger, Silke, Schorderet, Daniel F.
Publicado 2013

Senescent Changes and Topography of the Dark-Adapted Multifocal Electroretinogram

por Panorgias, Athanasios, Tillman, Megan, Sutter, Erich E., Moshiri, Ala, Gerth-Kahlert, Christina, Werner, John S.
Publicado 2017

Spontaneous Nystagmus in the Dark in an Infantile Nystagmus Patient May Represent Negative Optokinetic Afternystagmus

por Lin, Ting-Feng, Gerth-Kahlert, Christina, Hanson, James V. M., Straumann, Dominik, Huang, Melody Ying-Yu
Publicado 2018

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

por Bolognini, Ramona, Gerth-Kahlert, Christina, Abegg, Mathias, Bartholdi, Deborah, Mathis, Nicolas, Sturm, Veit, Gallati, Sabina, Schaller, André
Publicado 2017

Outcome of Pediatric Cataract Surgeries in a Tertiary Center in Switzerland

por Ambroz, Sarah Claudia, Töteberg-Harms, Marc, Hanson, James V. M., Funk, Jens, Barthelmes, Daniel, Gerth-Kahlert, Christina
Publicado 2018

Confirmation of Ogden syndrome as an X‐linked recessive fatal disorder due to a recurrent NAA10 variant and review of the literature

por Gogoll, Laura, Steindl, Katharina, Joset, Pascal, Zweier, Markus, Baumer, Alessandra, Gerth‐Kahlert, Christina, Tutschek, Boris, Rauch, Anita
Publicado 2021

Flicker electroretinogram in newborn infants

por Hanson, James V. M., Weber, Caroline, Pfäffli, Oliver A., Bassler, Dirk, McCulloch, Daphne L., Gerth-Kahlert, Christina
Publicado 2022

Functional Analysis of a Novel, Non-Canonical RPGR Splice Variant Causing X-Linked Retinitis Pigmentosa

por Koller, Samuel, Beltraminelli, Tim, Maggi, Jordi, Wlodarczyk, Agnès, Feil, Silke, Baehr, Luzy, Gerth-Kahlert, Christina, Menghini, Moreno, Berger, Wolfgang
Publicado 2023

A three-year longitudinal study of retinal function and structure in patients with multiple sclerosis

por Hanson, James V. M., Ng, Mei-Yee, Hayward-Koennecke, Helen K., Schippling, Sven, Reeve, Kelly A., Gerth-Kahlert, Christina
Publicado 2021

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

por Manogaran, Praveena, Hanson, James V. M., Olbert, Elisabeth D., Egger, Christine, Wicki, Carla, Gerth-Kahlert, Christina, Landau, Klara, Schippling, Sven
Publicado 2016

Functional and Morphological Characteristics of the Retina of Patients with Drusen-like Deposits and Systemic Lupus Erythematosus Treated with Hydroxychloroquine: A Retrospective S...

por Kitay, Alice M., Hanson, James V. M., Hasan, Nasiq, Driban, Matthew, Chhablani, Jay, Barthelmes, Daniel, Gerth-Kahlert, Christina, Al-Sheikh, Mayss
Publicado 2023

Long-Range PCR-Based NGS Applications to Diagnose Mendelian Retinal Diseases

por Maggi, Jordi, Koller, Samuel, Bähr, Luzy, Feil, Silke, Kivrak Pfiffner, Fatma, Hanson, James V. M., Maspoli, Alessandro, Gerth-Kahlert, Christina, Berger, Wolfgang
Publicado 2021

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

por Kivrak Pfiffner, Fatma, Koller, Samuel, Ménétrey, Anika, Graf, Urs, Bähr, Luzy, Maspoli, Alessandro, Hackenberg, Annette, Kottke, Raimund, Gerth-Kahlert, Christina, Berger, Wolfgang
Publicado 2022

Next generation sequencing based identification of disease-associated mutations in Swiss patients with retinal dystrophies

por Tiwari, Amit, Bahr, Angela, Bähr, Luzy, Fleischhauer, Johannes, Zinkernagel, Martin S., Winkler, Niklas, Barthelmes, Daniel, Berger, Lieselotte, Gerth-Kahlert, Christina, Neidhardt, John, Berger, Wolfgang
Publicado 2016

Whole Exome Sequencing in Coloboma/Microphthalmia: Identification of Novel and Recurrent Variants in Seven Genes

por Haug, Patricia, Koller, Samuel, Maggi, Jordi, Lang, Elena, Feil, Silke, Wlodarczyk, Agnès, Bähr, Luzy, Steindl, Katharina, Rohrbach, Marianne, Gerth-Kahlert, Christina, Berger, Wolfgang
Publicado 2021

Exome Sequencing in a Swiss Childhood Glaucoma Cohort Reveals CYP1B1 and FOXC1 Variants as Most Frequent Causes

por Lang, Elena, Koller, Samuel, Bähr, Luzy, Töteberg-Harms, Marc, Atac, David, Roulez, Françoise, Bahr, Angela, Steindl, Katharina, Feil, Silke, Berger, Wolfgang, Gerth-Kahlert, Christina
Publicado 2020

Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single center

por Gerth-Kahlert, Christina, Williamson, Kathleen, Ansari, Morad, Rainger, Jacqueline K, Hingst, Volker, Zimmermann, Theodor, Tech, Stefani, Guthoff, Rudolf F, van Heyningen, Veronica, FitzPatrick, David R
Publicado 2013