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Showing results (271-280 of 293) with videos related to

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JAMA Ophthalmology|July 6, 2023
Association of Risk Variants in the CFH Gene With Elevated Levels of Coagulation and Complement Factors in Idiopathic Multifocal ChoroiditisEvianne L de Groot, Jeannette Ossewaarde-van Norel, Joke H de Boer, et al.
JAMA Ophthalmology|April 20, 2023
Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular DegenerationJoel T Rämö, Erik Abner, Elon H C van Dijk, et al.
Retina (Philadelphia, Pa.)|April 18, 2020
CLINICAL CHARACTERISTICS AND NATURAL HISTORY OF RHO-ASSOCIATED RETINITIS PIGMENTOSA: A Long-Term Follow-Up StudyXuan-Thanh-An Nguyen, Mays Talib, Caroline van Cauwenbergh, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|October 17, 2025
International consensuses and guidelines on central serous chorioretinopathy (CSC) by the Asia Pacific Vitreo-retina Society (APVRS), the Academy of Asia-Pacific Professors of Ophthalmology (AAPPO) and the Academia Retina Internationalis (ARI)Nishant V Radke, Elon H C van Dijk, Richard F Spaide, et al.
Nature Genetics|December 23, 2015
Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrityNicole T M Saksens, Mark P Krebs, Frederieke E Schoenmaker-Koller, et al.
Investigative Ophthalmology & Visual Science|August 27, 2024
Frequency and Genetic Spectrum of Inherited Retinal Dystrophies in a Large Dutch Pediatric Cohort: The RD5000 ConsortiumPam A T Heutinck, L Ingeborgh van den Born, Maikel Vermeer, et al.
Nature Genetics|May 21, 2013
A functional variant in the CFI gene confers a high risk of age-related macular degenerationJohannes P H van de Ven, Sara C Nilsson, Perciliz L Tan, et al.
Communications Biology|December 25, 2019
Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathyYoshikatsu Hosoda, Masahiro Miyake, Rosa L Schellevis, et al.
Ophthalmology|October 8, 2021
X-Linked Retinoschisis: Novel Clinical Observations and Genetic Spectrum in 340 PatientsLeo C Hahn, Mary J van Schooneveld, Nieneke L Wesseling, et al.
Scientific Reports|March 18, 2025
Genome-wide association and multi-omics analyses provide insights into the disease mechanisms of central serous chorioretinopathyYuki Mori, Elon H C van Dijk, Masahiro Miyake, et al.
Pageof 30

Showing results (271-280 of 293) with videos related to

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Pageof 30
JAMA Ophthalmology|July 6, 2023
Association of Risk Variants in the CFH Gene With Elevated Levels of Coagulation and Complement Factors in Idiopathic Multifocal ChoroiditisEvianne L de Groot, Jeannette Ossewaarde-van Norel, Joke H de Boer, et al.
JAMA Ophthalmology|April 20, 2023
Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular DegenerationJoel T Rämö, Erik Abner, Elon H C van Dijk, et al.
Retina (Philadelphia, Pa.)|April 18, 2020
CLINICAL CHARACTERISTICS AND NATURAL HISTORY OF RHO-ASSOCIATED RETINITIS PIGMENTOSA: A Long-Term Follow-Up StudyXuan-Thanh-An Nguyen, Mays Talib, Caroline van Cauwenbergh, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|October 17, 2025
International consensuses and guidelines on central serous chorioretinopathy (CSC) by the Asia Pacific Vitreo-retina Society (APVRS), the Academy of Asia-Pacific Professors of Ophthalmology (AAPPO) and the Academia Retina Internationalis (ARI)Nishant V Radke, Elon H C van Dijk, Richard F Spaide, et al.
Nature Genetics|December 23, 2015
Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrityNicole T M Saksens, Mark P Krebs, Frederieke E Schoenmaker-Koller, et al.
Investigative Ophthalmology & Visual Science|August 27, 2024
Frequency and Genetic Spectrum of Inherited Retinal Dystrophies in a Large Dutch Pediatric Cohort: The RD5000 ConsortiumPam A T Heutinck, L Ingeborgh van den Born, Maikel Vermeer, et al.
Nature Genetics|May 21, 2013
A functional variant in the CFI gene confers a high risk of age-related macular degenerationJohannes P H van de Ven, Sara C Nilsson, Perciliz L Tan, et al.
Communications Biology|December 25, 2019
Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathyYoshikatsu Hosoda, Masahiro Miyake, Rosa L Schellevis, et al.
Ophthalmology|October 8, 2021
X-Linked Retinoschisis: Novel Clinical Observations and Genetic Spectrum in 340 PatientsLeo C Hahn, Mary J van Schooneveld, Nieneke L Wesseling, et al.
Scientific Reports|March 18, 2025
Genome-wide association and multi-omics analyses provide insights into the disease mechanisms of central serous chorioretinopathyYuki Mori, Elon H C van Dijk, Masahiro Miyake, et al.
Pageof 30