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Christina Zeitz

Showing results (11-20 of 155) with videos related to

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Documenta Ophthalmologica. Advances in Ophthalmology|March 21, 2015
Aripiprazole-induced chorioretinopathy: multimodal imaging and electrophysiological featuresCéline Faure, Isabelle Audo, Christina Zeitz, et al.
Biomed Research International|June 1, 2018
A Novel Heterozygous Missense Mutation in <i>GNAT1</i> Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night BlindnessChristina Zeitz, Cécile Méjécase, Mathilde Stévenard, et al.
European Journal of Human Genetics : EJHG|November 14, 2020
The genetics of rod-cone dystrophy in Arab countries: a systematic reviewLama Jaffal, Hawraa Joumaa, Zamzam Mrad, et al.
Retinal Cases & Brief Reports|September 22, 2025
Idiopathic Acute Exudative Polymorphous Vitelliform Maculopathy: A five-year follow-upRémi Pyra, Isabelle Audo, Hajar Jebrane, et al.
Investigative Ophthalmology & Visual Science|September 26, 2003
NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface proteinChristina Zeitz, Harry Scherthan, Susanne Freier, et al.
Orphanet Journal of Rare Diseases|April 24, 2022
The research output of rod-cone dystrophy geneticsLama Jaffal, Zamzam Mrad, Mariam Ibrahim, et al.
Ophthalmic Genetics|October 23, 2025
Identification of a novel <i>CABP4</i> frameshift variant and a secondary <i>USH2A</i> missense variant in congenital cone-rod synaptic disorderZahraa Mousawi, Alain Chebly, Joseph Nehme, et al.
Acta Ophthalmologica|June 24, 2025
Genetic analysis of congenital stationary night blindness and Oguchi disease in an Indian cohortSrilekha Sundaramurthy, Sivasankar Malaichamy, Parveen Sen, et al.
Retina (Philadelphia, Pa.)|January 26, 2018
AUTOSOMAL DOMINANT VITREORETINOCHOROIDOPATHY: When Molecular Genetic Testing Helps Clinical DiagnosisElise Boulanger-Scemama, Jose-Alain Sahel, Saddek Mohand-Said, et al.
Molecular Vision|March 12, 2005
Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindnessChristina Zeitz, Roberta Minotti, Silke Feil, et al.
Pageof 16

Showing results (11-20 of 155) with videos related to

Sort By:
Pageof 16
Documenta Ophthalmologica. Advances in Ophthalmology|March 21, 2015
Aripiprazole-induced chorioretinopathy: multimodal imaging and electrophysiological featuresCéline Faure, Isabelle Audo, Christina Zeitz, et al.
Biomed Research International|June 1, 2018
A Novel Heterozygous Missense Mutation in <i>GNAT1</i> Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night BlindnessChristina Zeitz, Cécile Méjécase, Mathilde Stévenard, et al.
European Journal of Human Genetics : EJHG|November 14, 2020
The genetics of rod-cone dystrophy in Arab countries: a systematic reviewLama Jaffal, Hawraa Joumaa, Zamzam Mrad, et al.
Retinal Cases & Brief Reports|September 22, 2025
Idiopathic Acute Exudative Polymorphous Vitelliform Maculopathy: A five-year follow-upRémi Pyra, Isabelle Audo, Hajar Jebrane, et al.
Investigative Ophthalmology & Visual Science|September 26, 2003
NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface proteinChristina Zeitz, Harry Scherthan, Susanne Freier, et al.
Orphanet Journal of Rare Diseases|April 24, 2022
The research output of rod-cone dystrophy geneticsLama Jaffal, Zamzam Mrad, Mariam Ibrahim, et al.
Ophthalmic Genetics|October 23, 2025
Identification of a novel <i>CABP4</i> frameshift variant and a secondary <i>USH2A</i> missense variant in congenital cone-rod synaptic disorderZahraa Mousawi, Alain Chebly, Joseph Nehme, et al.
Acta Ophthalmologica|June 24, 2025
Genetic analysis of congenital stationary night blindness and Oguchi disease in an Indian cohortSrilekha Sundaramurthy, Sivasankar Malaichamy, Parveen Sen, et al.
Retina (Philadelphia, Pa.)|January 26, 2018
AUTOSOMAL DOMINANT VITREORETINOCHOROIDOPATHY: When Molecular Genetic Testing Helps Clinical DiagnosisElise Boulanger-Scemama, Jose-Alain Sahel, Saddek Mohand-Said, et al.
Molecular Vision|March 12, 2005
Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindnessChristina Zeitz, Roberta Minotti, Silke Feil, et al.
Pageof 16