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Showing results (61-70 of 85) with videos related to

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JIMD Reports|December 8, 2017
Effect of Storage Conditions on Stability of Ophthalmological Compounded Cysteamine Eye DropsAhmed Reda, Ann Van Schepdael, Erwin Adams, et al.
Eye (London, England)|August 1, 2019
Retinopathy of prematurity in Rwanda: a prospective multi-centre study following introduction of screening and treatment servicesFrancis Mutangana, Charles Muhizi, Godelieve Mudereva, et al.
Eye (London, England)|September 6, 2019
Correction: Retinopathy of prematurity in Rwanda: a prospective multi-centre study following introduction of screening and treatment servicesFrancis Mutangana, Charles Muhizi, Godelieve Mudereva, et al.
Journal of Clinical Immunology|May 5, 2021
Hematopoietic Stem Cell Transplantation Cures Chronic Aichi Virus Infection in a Patient with X-linked AgammaglobulinemiaGiorgia Bucciol, Thomas Tousseyn, Katrien Jansen, et al.
American Journal of Medical Genetics. Part A|January 31, 2014
Sclerocornea in a patient with van den Ende-Gupta syndrome homozygous for a SCARF2 microdeletionMichele P Migliavacca, Nara L M Sobreira, Graziela P M Antonialli, et al.
Investigative Ophthalmology & Visual Science|September 27, 2014
Nature of the visual loss in observers with Leber's congenital amaurosis caused by specific mutations in RPE65Caterina Ripamonti, G Bruce Henning, Robin R Ali, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 15, 2014
Identity-by-descent-guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophyFrauke Coppieters, Kristof Van Schil, Miriam Bauwens, et al.
Journal of Vision|November 26, 2015
Spectral sensitivity measurements reveal partial success in restoring missing rod function with gene therapyCaterina Ripamonti, G Bruce Henning, Scott J Robbie, et al.
Plos One|January 12, 2017
Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian FamiliesCaroline Van Cauwenbergh, Frauke Coppieters, Dimitri Roels, et al.
American Journal of Human Genetics|January 9, 2008
Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16Irina Balikova, Kevin Martens, Cindy Melotte, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
JIMD Reports|December 8, 2017
Effect of Storage Conditions on Stability of Ophthalmological Compounded Cysteamine Eye DropsAhmed Reda, Ann Van Schepdael, Erwin Adams, et al.
Eye (London, England)|August 1, 2019
Retinopathy of prematurity in Rwanda: a prospective multi-centre study following introduction of screening and treatment servicesFrancis Mutangana, Charles Muhizi, Godelieve Mudereva, et al.
Eye (London, England)|September 6, 2019
Correction: Retinopathy of prematurity in Rwanda: a prospective multi-centre study following introduction of screening and treatment servicesFrancis Mutangana, Charles Muhizi, Godelieve Mudereva, et al.
Journal of Clinical Immunology|May 5, 2021
Hematopoietic Stem Cell Transplantation Cures Chronic Aichi Virus Infection in a Patient with X-linked AgammaglobulinemiaGiorgia Bucciol, Thomas Tousseyn, Katrien Jansen, et al.
American Journal of Medical Genetics. Part A|January 31, 2014
Sclerocornea in a patient with van den Ende-Gupta syndrome homozygous for a SCARF2 microdeletionMichele P Migliavacca, Nara L M Sobreira, Graziela P M Antonialli, et al.
Investigative Ophthalmology & Visual Science|September 27, 2014
Nature of the visual loss in observers with Leber's congenital amaurosis caused by specific mutations in RPE65Caterina Ripamonti, G Bruce Henning, Robin R Ali, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 15, 2014
Identity-by-descent-guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophyFrauke Coppieters, Kristof Van Schil, Miriam Bauwens, et al.
Journal of Vision|November 26, 2015
Spectral sensitivity measurements reveal partial success in restoring missing rod function with gene therapyCaterina Ripamonti, G Bruce Henning, Scott J Robbie, et al.
Plos One|January 12, 2017
Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian FamiliesCaroline Van Cauwenbergh, Frauke Coppieters, Dimitri Roels, et al.
American Journal of Human Genetics|January 9, 2008
Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16Irina Balikova, Kevin Martens, Cindy Melotte, et al.
Pageof 9