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Christina Gerth

Showing results (71-80 of 85) with videos related to

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Translational Vision Science & Technology|August 25, 2020
Exome Sequencing in a Swiss Childhood Glaucoma Cohort Reveals <i>CYP1B1</i> and <i>FOXC1</i> Variants as Most Frequent CausesElena Lang, Samuel Koller, Luzy Bähr, et al.
Human Molecular Genetics|November 8, 2019
Atonal homolog 7 (ATOH7) loss-of-function mutations in predominant bilateral optic nerve hypoplasiaDavid Atac, Samuel Koller, James V M Hanson, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single centerChristina Gerth-Kahlert, Kathleen Williamson, Morad Ansari, et al.
American Journal of Ophthalmology|June 16, 2024
The Effect of Perinatal High-Dose Erythropoietin on Retinal Structural and Vascular Characteristics in Children Born PretermBrida M Jeltsch, James V M Hanson, Jonas Füglistaler, et al.
American Journal of Ophthalmology|July 12, 2024
The Effect of High-Dose Erythropoietin Perinatally on Retinal Function in School-Aged Children Born Extremely or Very PretermLorena Sisera, James V M Hanson, Jonas Füglistaler, et al.
Human Molecular Genetics|February 9, 2022
Multisystem involvement, defective lysosomes and impaired autophagy in a novel rat model of nephropathic cystinosisPatrick Krohn, Laura Rita Rega, Marianne Harvent, et al.
Clinical Genetics|November 17, 2025
The Phenotypic and Genotypic Features of ADAMTSL4-Related Ocular DiseaseKatie M Williams, Wolfgang Berger, Samuel Koller, et al.
Acta Ophthalmologica|September 30, 2020
Genotype-phenotype spectrum in isolated and syndromic nanophthalmosElena Lang, Samuel Koller, David Atac, et al.
Journal of Medical Genetics|May 18, 2010
Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient populationGail Billingsley, Jenea Bin, Karen J Fieggen, et al.
JAMA Ophthalmology|May 20, 2021
Genetic Analysis in a Swiss Cohort of Bilateral Congenital CataractDelia Rechsteiner, Lydia Issler, Samuel Koller, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
Translational Vision Science & Technology|August 25, 2020
Exome Sequencing in a Swiss Childhood Glaucoma Cohort Reveals <i>CYP1B1</i> and <i>FOXC1</i> Variants as Most Frequent CausesElena Lang, Samuel Koller, Luzy Bähr, et al.
Human Molecular Genetics|November 8, 2019
Atonal homolog 7 (ATOH7) loss-of-function mutations in predominant bilateral optic nerve hypoplasiaDavid Atac, Samuel Koller, James V M Hanson, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single centerChristina Gerth-Kahlert, Kathleen Williamson, Morad Ansari, et al.
American Journal of Ophthalmology|June 16, 2024
The Effect of Perinatal High-Dose Erythropoietin on Retinal Structural and Vascular Characteristics in Children Born PretermBrida M Jeltsch, James V M Hanson, Jonas Füglistaler, et al.
American Journal of Ophthalmology|July 12, 2024
The Effect of High-Dose Erythropoietin Perinatally on Retinal Function in School-Aged Children Born Extremely or Very PretermLorena Sisera, James V M Hanson, Jonas Füglistaler, et al.
Human Molecular Genetics|February 9, 2022
Multisystem involvement, defective lysosomes and impaired autophagy in a novel rat model of nephropathic cystinosisPatrick Krohn, Laura Rita Rega, Marianne Harvent, et al.
Clinical Genetics|November 17, 2025
The Phenotypic and Genotypic Features of ADAMTSL4-Related Ocular DiseaseKatie M Williams, Wolfgang Berger, Samuel Koller, et al.
Acta Ophthalmologica|September 30, 2020
Genotype-phenotype spectrum in isolated and syndromic nanophthalmosElena Lang, Samuel Koller, David Atac, et al.
Journal of Medical Genetics|May 18, 2010
Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient populationGail Billingsley, Jenea Bin, Karen J Fieggen, et al.
JAMA Ophthalmology|May 20, 2021
Genetic Analysis in a Swiss Cohort of Bilateral Congenital CataractDelia Rechsteiner, Lydia Issler, Samuel Koller, et al.
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