Gerth-Kahlert, Christina: search on Z-Library

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1

Incidence of retinopathy of prematurity (ROP) and ROP treatment in Switzerland 2006–2015: a population-based analysis

Gerull, Roland, Brauer, Viviane, Bassler, Dirk, Laubscher, Bernard, Pfister, Riccardo E, Nelle, Mathias, Müller, Béatrice, Gerth-Kahlert, Christina, Adams, Mark

Journal:

Archives of Disease in Childhood - Fetal and Neonatal Edition

Year:

2017

Language:

english

File:

PDF, 1.01 MB

english, 2017

2

Senescent Changes and Topography of the Dark-Adapted Multifocal Electroretinogram

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

Journal:

Investigative Opthalmology & Visual Science

Year:

2017

Language:

english

File:

PDF, 798 KB

english, 2017

3

Discriminative validity of color vision tests in young children: comparison of normal and impaired vision subjects

Pfaeffli, Oliver A., Gerth-Kahlert, Christina

Journal:

Journal of American Association for Pediatric Ophthalmology and Strabismus

Year:

2018

Language:

english

File:

PDF, 40 KB

english, 2018

4

Outcome of Pediatric Cataract Surgeries in a Tertiary Center in Switzerland

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

Journal:

Journal of Ophthalmology

Year:

2018

Language:

english

File:

PDF, 1.89 MB

english, 2018

5

Alternating IV Nerve Palsy and Ptosis as a First Sign of Childhood Ocular Myasthenia Gravis

Chappaz, Ariane, Knirsch, Ursula, Gerth-Kahlert, Christina

Journal:

Pediatric Neurology

Year:

2015

Language:

english

File:

PDF, 911 KB

english, 2015

6

A secreted WNT-ligand-binding domain of FZD5 generated by a frameshift mutation causes autosomal dominant coloboma

Liu, Chunqiao, Widen, Sonya A., Williamson, Kathleen A., Ratnapriya, Rinki, Gerth-Kahlert, Christina, Rainger, Joe, Alur, Ramakrishna P., Strachan, Erin, Manjunath, Souparnika H., Balakrishnan, Archan

Journal:

Human Molecular Genetics

Year:

2016

Language:

english

File:

PDF, 921 KB

english, 2016

7

Congenital Lamellar Cataract

Gerth-Kahlert, Christina, Michels, Rike, Funk, Jens, Gautschy, Ursula

Journal:

JAMA Ophthalmology

Year:

2014

Language:

english

File:

PDF, 110 KB

english, 2014

8

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

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

Journal:

Frontiers in Neurology

Year:

2018

Language:

english

File:

PDF, 1.10 MB

english, 2018

9

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

Hanson, James V. M., Hediger, Michael, Manogaran, Praveena, Landau, Klara, Hagenbuch, Niels, Schippling, Sven, Gerth-Kahlert, Christina

Journal:

Investigative Opthalmology & Visual Science

Year:

2018

Language:

english

File:

PDF, 1.49 MB

english, 2018

10

Cocaine test results in children with anisocoria

Fierz, Fabienne C., Gerth-Kahlert, Christina

Journal:

Journal of American Association for Pediatric Ophthalmology and Strabismus

Year:

2016

Language:

english

File:

PDF, 41 KB

english, 2016

11

Retinale Ziliopathien

Gerth-Kahlert, Christina, Koller, Samuel

Journal:

Klinische Monatsblätter für Augenheilkunde

Year:

2018

Language:

german

File:

PDF, 313 KB

german, 2018

12

Infantile hemangiomas with conjunctival involvement: An underreported occurrence

Theiler, Martin, Baselga, Eulalia, Gerth-Kahlert, Christina, Mathes, Erin F., Schwieger-Briel, Agnes, Chaloupka, Karla, Weibel, Lisa, Frieden, Ilona J.

Journal:

Pediatric Dermatology

Year:

2017

Language:

english

File:

PDF, 452 KB

english, 2017

13

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

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

Journal:

Frontiers in Neurology

Year:

2020

File:

PDF, 190 KB

2020

14

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

Gerth-Kahlert, Christina, Williamson, Kathleen, Ansari, Morad, Rainger, Jacqueline K., Hingst, Volker, Zimmermann, Theodor, Tech, Stefani, Guthoff, Rudolf F., van Heyningen, Veronica, FitzPatrick, Dav

Journal:

Molecular Genetics & Genomic Medicine

Year:

2013

Language:

english

File:

PDF, 449 KB

english, 2013

15

Absence of Goniodysgenesis in Patients with Chromosome 13Q Microdeletion-Related Microcoria

Gerth-Kahlert, Christina, Maggi, Jordi, TÃ¶teberg-Harms, Marc, Tiwari, Amit, Budde, Birgit, NÃ¼rnberg, Peter, Koller, Samuel, Berger, Wolfgang

Journal:

Ophthalmology Glaucoma

Year:

2018

File:

PDF, 554 KB

2018

16

Isolated and syndromal severe congenital eye malformations: Genotype- phenotype analysis in patients with anophthalmia or microphthalmia

Christina Gerth-Kahlert

Journal:

Journal of American Association for Pediatric Ophthalmology and Strabismus

Year:

2012

Language:

english

File:

PDF, 39 KB

english, 2012

17

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

Fierz, Fabienne C., Gerth-Kahlert, Christina

Journal:

Journal of Ophthalmology

Year:

2017

Language:

english

File:

PDF, 1.29 MB

english, 2017

18

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

Lang, Elena, Koller, Samuel, BÃ¤hr, Luzy, TÃ¶teberg-Harms, Marc, Atac, David, Roulez, FranÃ§oise, Bahr, Angela, Steindl, Katharina, Feil, Silke, Berger, Wolfgang, Gerth-Kahlert, Christina

Journal:

Translational Vision Science & Technology

Year:

2020

File:

PDF, 674 KB

2020

19

Optic Disc Doubling or Pseudo-Optic Disc in Colobomatous Retinal Abnormality?

Gerth-Kahlert, Christina, Wildberger, Hannes

Journal:

Journal of Neuro-Ophthalmology

Year:

2013

Language:

english

File:

PDF, 195 KB

english, 2013

20

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

Hanson, James V. M., Hediger, Michael, Manogaran, Praveena, Landau, Klara, Hagenbuch, Niels, Schippling, Sven, Gerth-Kahlert, Christina

Journal:

Investigative Opthalmology & Visual Science

Year:

2018

File:

PDF, 1.49 MB

2018

21

Bilateral vitreous hemorrhage in a newborn with Stickler syndrome associated with a novel COL2A1 mutation

Christina Gerth-Kahlert, Salvatore Grisanti, Eike Berger, Rene Höhn, Gabriele Witt, Ursula Jung

Journal:

Journal of American Association for Pediatric Ophthalmology and Strabismus

Year:

2011

Language:

english

File:

PDF, 424 KB

english, 2011

22

Genotype–Phenotype Analysis of a Novel Recessive and a Recurrent Dominant SNRNP200 Variant Causing Retinitis Pigmentosa

Gerth-Kahlert, Christina, Koller, Samuel, Hanson, James V. M., Baehr, Luzy, Tiwari, Amit, Kivrak-Pfiffner, Fatma, Bahr, Angela, Berger, Wolfgang

Journal:

Investigative Opthalmology & Visual Science

Year:

2019

Language:

english

File:

PDF, 1.59 MB

english, 2019

23

Teaching Neuro Images : Recurrent oculomotor palsies caused by neurosarcoidosis

Kana, Veronika, Petersen, Jens A., Ikenberg, Kristian, Chappaz, Ariane, Gerth-Kahlert, Christina, Appenzeller, Philippe, Linnebank, Michael

Journal:

Year:

2016

Language:

english

File:

PDF, 457 KB

english, 2016

24

Biallelic Mutations in CRB1 Underlie Autosomal Recessive Familial Foveal Retinoschisis

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, Heathe

Journal:

Investigative Opthalmology & Visual Science

Year:

2016

Language:

english

File:

PDF, 1.21 MB

english, 2016

25

Clinical utility gene card for: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches

Richardson, Rose, Sowden, Jane, Gerth-Kahlert, Christina, Moore, Anthony T, Moosajee, Mariya

Journal:

European Journal of Human Genetics

Year:

2017

Language:

english

File:

PDF, 174 KB

english, 2017

26

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

Manogaran, Praveena, Hanson, James, Olbert, Elisabeth, Egger, Christine, Wicki, Carla, Gerth-Kahlert, Christina, Landau, Klara, Schippling, Sven

Journal:

International Journal of Molecular Sciences

Year:

2016

Language:

english

File:

PDF, 1.42 MB

english, 2016

27

Iris cyst in a child with Aicardi syndrome: a novel association

Chappaz, Ariane, Barthelmes, Daniel, Buser, Lorenz, Funk, Jens, Gerth-Kahlert, Christina

Journal:

Journal of American Association for Pediatric Ophthalmology and Strabismus

Year:

2016

Language:

english

File:

PDF, 702 KB

english, 2016

28

Complex optic nerve and macular hypoplasia in two siblings with compound heterozygous mutations in the ATOH7 gene

Gerth-Kahlert, Christina, Tiwari, Amit, Bahr, Angela, Bähr, Luzy, Magyar, István, Berger, Wolfgang

Journal:

Journal of American Association for Pediatric Ophthalmology and Strabismus

Year:

2016

Language:

english

File:

PDF, 44 KB

english, 2016

29

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

Ramona Bolognini,Christina Gerth-Kahlert,Mathias Abegg…

Journal:

BMC Medical Genetics

Year:

2017

Language:

english

File:

PDF, 1.87 MB

english, 2017

30

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

Atac, David Grubich, Koller, Samuel, Hanson, James V M, Feil, Silke, Tiwari, Amit, Bahr, Angela, Baehr, Luzy, Magyar, István, Kottke, Raimund, Gerth-Kahlert, Christina, Berger, Wolfgang

Journal:

Human Molecular Genetics

Year:

2019

Language:

english

File:

PDF, 1.55 MB

english, 2019

31

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

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

Journal:

Scientific Reports

Year:

2016

Language:

english

File:

PDF, 1.45 MB

english, 2016

32

Horizontal Gaze Palsy in Two Brothers with Compound Heterozygous ROBO3 Gene Mutations

Hackenberg, Annette, Boltshauser, Eugen, Gerth-Kahlert, Christina, Stahr, Nikolai, Azzarello-Burri, Silvia, Plecko, Barbara

Journal:

Neuropediatrics

Year:

2016

Language:

english

File:

PDF, 137 KB

english, 2016

33

Prediction of ROP Treatment and Evaluation of Screening Criteria in VLBW Infants–a Population Based Analysis

Brauer, Viviane, Gerull, Roland, Bassler, Dirk, Laubscher, Bernard, Pfister, Riccardo E, Nelle, Mathias, Müller, Beatrice, Roth-Kleiner, Matthias, Gerth-Kahlert, Christina, Adams, Mark

Journal:

Pediatric Research

Year:

2018

Language:

english

File:

PDF, 633 KB

english, 2018

34

Maculopathy following exposure to visible and infrared radiation from a laser pointer: a clinical case study

Hanson, James V. M., Sromicki, Julian, Mangold, Mario, Golling, Matthias, Gerth-Kahlert, Christina

Journal:

Documenta Ophthalmologica

Year:

2016

Language:

english

File:

PDF, 1.34 MB

english, 2016

35

Unusual retinopathy in a child with severe combined immune deficiency

Gerth-Kahlert, Christina, Tiwari, Amit, Hauri-Hohl, Mathias M., Hanson, James V. M., Bahr, Angela, Palmowski-Wolfe, Anja, Güngör, Tayfun, Berger, Wolfgang

Journal:

Ophthalmic Genetics

Year:

2017

Language:

english

File:

PDF, 655 KB

english, 2017

36

Retinal Ganglion Cell Topography in Patients With Visual Pathway Pathology

Zehnder, Simon, Wildberger, Hannes, Hanson, James V. M., Lukas, Sebastian, Pelz, Stefan, Landau, Klara, Wichmann, Werner, Gerth-Kahlert, Christina

Journal:

Journal of Neuro-Ophthalmology

Year:

2017

Language:

english

File:

PDF, 1.01 MB

english, 2017

37

C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations

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

Journal:

Investigative Opthalmology & Visual Science

Year:

2017

Language:

english

File:

PDF, 847 KB

english, 2017

38

Tuberöse-Sklerose-Komplex: Analyse des okulären Phänotyps und assoziierter Komplikationen

Zweipfenning, Florian, Toelle, Sandra, Gerth-Kahlert, Christina

Journal:

Klinische Monatsblätter für Augenheilkunde

Year:

2019

File:

PDF, 246 KB

2019

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