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Christina Gerth

Showing results (21-30 of 85) with videos related to

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Plos One|November 7, 2013
Dental phenotype in Jalili syndrome due to a c.1312 dupC homozygous mutation in the CNNM4 geneHans U Luder, Christina Gerth-Kahlert, Silke Ostertag-Benzinger, et al.
Acta Ophthalmologica|August 31, 2019
Colour vision testing in young children with reduced visual acuityOliver Andreas Pfäffli, Bálint Tamási, James V M Hanson, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 13, 2024
Visual outcome measures in pediatric myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD)Flavia C Gericke, James V M Hanson, Annette Hackenberg, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|February 18, 2026
Functional and structural outcomes in paediatric myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD): a prospective studyFlavia C Gericke, James V M Hanson, Annette Hackenberg, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 15, 2006
Cone-mediated multifocal electroretinogram in age-related macular degeneration: progression over a long-term follow-upChristina Gerth, Peter B Delahunt, Suhail Alam, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 15, 2003
Assessment of multifocal electroretinogram abnormalities and their relation to morphologic characteristics in patients with large drusenChristina Gerth, David Hauser, Peter B Delahunt, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 6, 2002
Multifocal electroretinogram: age-related changes for different luminance levelsChristina Gerth, Susan M Garcia, Lei Ma, et al.
International Journal of Molecular Sciences|December 9, 2023
Novel <i>CRYGC</i> Mutation in Conserved Ultraviolet-Protective Tryptophan (p.Trp131Arg) Is Linked to Autosomal Dominant Congenital CataractFlora Delas, Samuel Koller, Silke Feil, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 29, 2020
Higher incidence of retinopathy of prematurity in extremely preterm infants associated with improved survival ratesAylin Taner, Senait Tekle, Torsten Hothorn, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|July 23, 2011
Bilateral vitreous hemorrhage in a newborn with Stickler syndrome associated with a novel COL2A1 mutationChristina Gerth-Kahlert, Salvatore Grisanti, Eike Berger, et al.
Pageof 9

Showing results (21-30 of 85) with videos related to

Sort By:
Pageof 9
Plos One|November 7, 2013
Dental phenotype in Jalili syndrome due to a c.1312 dupC homozygous mutation in the CNNM4 geneHans U Luder, Christina Gerth-Kahlert, Silke Ostertag-Benzinger, et al.
Acta Ophthalmologica|August 31, 2019
Colour vision testing in young children with reduced visual acuityOliver Andreas Pfäffli, Bálint Tamási, James V M Hanson, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 13, 2024
Visual outcome measures in pediatric myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD)Flavia C Gericke, James V M Hanson, Annette Hackenberg, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|February 18, 2026
Functional and structural outcomes in paediatric myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD): a prospective studyFlavia C Gericke, James V M Hanson, Annette Hackenberg, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 15, 2006
Cone-mediated multifocal electroretinogram in age-related macular degeneration: progression over a long-term follow-upChristina Gerth, Peter B Delahunt, Suhail Alam, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 15, 2003
Assessment of multifocal electroretinogram abnormalities and their relation to morphologic characteristics in patients with large drusenChristina Gerth, David Hauser, Peter B Delahunt, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 6, 2002
Multifocal electroretinogram: age-related changes for different luminance levelsChristina Gerth, Susan M Garcia, Lei Ma, et al.
International Journal of Molecular Sciences|December 9, 2023
Novel <i>CRYGC</i> Mutation in Conserved Ultraviolet-Protective Tryptophan (p.Trp131Arg) Is Linked to Autosomal Dominant Congenital CataractFlora Delas, Samuel Koller, Silke Feil, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 29, 2020
Higher incidence of retinopathy of prematurity in extremely preterm infants associated with improved survival ratesAylin Taner, Senait Tekle, Torsten Hothorn, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|July 23, 2011
Bilateral vitreous hemorrhage in a newborn with Stickler syndrome associated with a novel COL2A1 mutationChristina Gerth-Kahlert, Salvatore Grisanti, Eike Berger, et al.
Pageof 9