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Robert K Koenekoop

Showing results (11-20 of 122) with videos related to

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Ophthalmic Genetics|March 23, 2002
Visual improvement in Leber congenital amaurosis and the CRX genotypeRobert K Koenekoop, Magali Loyer, Olga Dembinska, et al.
Molecular Vision|April 20, 2004
A three base pair deletion encoding the amino acid (lysine-270) in the alpha-cone transducin geneAna Luisa Piña, Uwe Baumert, Magali Loyer, et al.
American Journal of Medical Genetics. Part A|August 8, 2019
Maternally inherited MAF variant associated with variable expression of Aymé-Gripp syndromeEbba Alkhunaizi, Robert K Koenekoop, Christine Saint-Martin, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|October 1, 2009
Optimal compliance for amblyopia therapy: occlusion with a translucent tape on the lensRaquel G Beneish, Robert C Polomeno, Michael E Flanders, et al.
Journal of Clinical Medicine|September 27, 2025
Neural Network Prediction of Keratoconus in AIPL1-Linked Leber Congenital Amaurosis: A Proof-of-Concept Pilot StudyDaniel R Chow, Raheem Remtulla, Glenda Vargas, et al.
Ophthalmology|February 5, 2005
Clinical phenotypes in carriers of Leber congenital amaurosis mutationsJennifer A Galvin, Gerald A Fishman, Edwin M Stone, et al.
Retina (Philadelphia, Pa.)|October 6, 2005
Evaluation of genotype-phenotype associations in leber congenital amaurosisJennifer A Galvin, Gerald A Fishman, Edwin M Stone, et al.
Frontiers in Aging Neuroscience|November 12, 2020
The Relationship Between Cognitive Status and Known Single Nucleotide Polymorphisms in Age-Related Macular DegenerationCaitlin Murphy, Aaron P Johnson, Robert K Koenekoop, et al.
Progress in Retinal and Eye Research|July 18, 2008
Leber congenital amaurosis: genes, proteins and disease mechanismsAnneke I den Hollander, Ronald Roepman, Robert K Koenekoop, et al.
Scientific Reports|January 3, 2025
Amblyopic binocular imbalance quantified by the dichoptic contrast ordering test and dichoptic letters testAlexandre Reynaud, Marie-Céline Lorenzini, Robert K Koenekoop, et al.
Pageof 13

Showing results (11-20 of 122) with videos related to

Sort By:
Pageof 13
Ophthalmic Genetics|March 23, 2002
Visual improvement in Leber congenital amaurosis and the CRX genotypeRobert K Koenekoop, Magali Loyer, Olga Dembinska, et al.
Molecular Vision|April 20, 2004
A three base pair deletion encoding the amino acid (lysine-270) in the alpha-cone transducin geneAna Luisa Piña, Uwe Baumert, Magali Loyer, et al.
American Journal of Medical Genetics. Part A|August 8, 2019
Maternally inherited MAF variant associated with variable expression of Aymé-Gripp syndromeEbba Alkhunaizi, Robert K Koenekoop, Christine Saint-Martin, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|October 1, 2009
Optimal compliance for amblyopia therapy: occlusion with a translucent tape on the lensRaquel G Beneish, Robert C Polomeno, Michael E Flanders, et al.
Journal of Clinical Medicine|September 27, 2025
Neural Network Prediction of Keratoconus in AIPL1-Linked Leber Congenital Amaurosis: A Proof-of-Concept Pilot StudyDaniel R Chow, Raheem Remtulla, Glenda Vargas, et al.
Ophthalmology|February 5, 2005
Clinical phenotypes in carriers of Leber congenital amaurosis mutationsJennifer A Galvin, Gerald A Fishman, Edwin M Stone, et al.
Retina (Philadelphia, Pa.)|October 6, 2005
Evaluation of genotype-phenotype associations in leber congenital amaurosisJennifer A Galvin, Gerald A Fishman, Edwin M Stone, et al.
Frontiers in Aging Neuroscience|November 12, 2020
The Relationship Between Cognitive Status and Known Single Nucleotide Polymorphisms in Age-Related Macular DegenerationCaitlin Murphy, Aaron P Johnson, Robert K Koenekoop, et al.
Progress in Retinal and Eye Research|July 18, 2008
Leber congenital amaurosis: genes, proteins and disease mechanismsAnneke I den Hollander, Ronald Roepman, Robert K Koenekoop, et al.
Scientific Reports|January 3, 2025
Amblyopic binocular imbalance quantified by the dichoptic contrast ordering test and dichoptic letters testAlexandre Reynaud, Marie-Céline Lorenzini, Robert K Koenekoop, et al.
Pageof 13