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Christina Zeitz

Showing results (1-10 of 155) with videos related to

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Documenta Ophthalmologica. Advances in Ophthalmology|July 28, 2018
Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic associationMichael F Marmor, Christina Zeitz
JAMA Ophthalmology|October 28, 2021
Challenges of Phenotype-Genotype Correlations in Rare Diseases-ReplyVasily M Smirnov, Christina Zeitz, Isabelle Audo
Progress in Retinal and Eye Research|October 14, 2014
Congenital stationary night blindness: an analysis and update of genotype-phenotype correlations and pathogenic mechanismsChristina Zeitz, Anthony G Robson, Isabelle Audo
Methods in Molecular Biology (Clifton, N.J.)|January 9, 2013
Arrayed primer extension microarray for the analysis of genes associated with congenital stationary night blindnessKadri Vaidla, Janne Uksti, Christina Zeitz, et al.
Cold Spring Harbor Perspectives in Medicine|August 21, 2023
The Extraordinary Phenotypic and Genetic Variability of Retinal and Macular Degenerations: The Relevance to Therapeutic DevelopmentsIsabelle Audo, Marco Nassisi, Christina Zeitz, et al.
Medecine Sciences : M/S|March 30, 2010
[TRPM1, a new gene implicated in congenital stationary night blindness]Isabelle Audo, José-Alain Sahel, Shomi Bhattacharya, et al.
Klinische Monatsblatter Fur Augenheilkunde|February 2, 2018
[Overview of Congenital Stationary Night Blindness with Predominantly Normal Fundus Appearance]Christina Zeitz, Christoph Friedburg, Markus N Preising, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|March 12, 2018
Retinal findings in a patient of French ancestry with CABP4-related retinal diseaseVasily Mikhaïlovitch Smirnov, Christina Zeitz, Nagasamy Soumittra, et al.
Human Mutation|April 4, 2007
Identification and characterization of a novel RPGR isoform in human retinaJohn Neidhardt, Esther Glaus, Daniel Barthelmes, et al.
Genes|April 17, 2018
Special Issue Introduction: Inherited Retinal Disease: Novel Candidate Genes, Genotype-Phenotype Correlations, and Inheritance ModelsFrans P M Cremers, Camiel J F Boon, Kinga Bujakowska, et al.
Pageof 16

Showing results (1-10 of 155) with videos related to

Sort By:
Pageof 16
Documenta Ophthalmologica. Advances in Ophthalmology|July 28, 2018
Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic associationMichael F Marmor, Christina Zeitz
JAMA Ophthalmology|October 28, 2021
Challenges of Phenotype-Genotype Correlations in Rare Diseases-ReplyVasily M Smirnov, Christina Zeitz, Isabelle Audo
Progress in Retinal and Eye Research|October 14, 2014
Congenital stationary night blindness: an analysis and update of genotype-phenotype correlations and pathogenic mechanismsChristina Zeitz, Anthony G Robson, Isabelle Audo
Methods in Molecular Biology (Clifton, N.J.)|January 9, 2013
Arrayed primer extension microarray for the analysis of genes associated with congenital stationary night blindnessKadri Vaidla, Janne Uksti, Christina Zeitz, et al.
Cold Spring Harbor Perspectives in Medicine|August 21, 2023
The Extraordinary Phenotypic and Genetic Variability of Retinal and Macular Degenerations: The Relevance to Therapeutic DevelopmentsIsabelle Audo, Marco Nassisi, Christina Zeitz, et al.
Medecine Sciences : M/S|March 30, 2010
[TRPM1, a new gene implicated in congenital stationary night blindness]Isabelle Audo, José-Alain Sahel, Shomi Bhattacharya, et al.
Klinische Monatsblatter Fur Augenheilkunde|February 2, 2018
[Overview of Congenital Stationary Night Blindness with Predominantly Normal Fundus Appearance]Christina Zeitz, Christoph Friedburg, Markus N Preising, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|March 12, 2018
Retinal findings in a patient of French ancestry with CABP4-related retinal diseaseVasily Mikhaïlovitch Smirnov, Christina Zeitz, Nagasamy Soumittra, et al.
Human Mutation|April 4, 2007
Identification and characterization of a novel RPGR isoform in human retinaJohn Neidhardt, Esther Glaus, Daniel Barthelmes, et al.
Genes|April 17, 2018
Special Issue Introduction: Inherited Retinal Disease: Novel Candidate Genes, Genotype-Phenotype Correlations, and Inheritance ModelsFrans P M Cremers, Camiel J F Boon, Kinga Bujakowska, et al.
Pageof 16