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American Journal of Ophthalmology
|
May 4, 2020
Choroidal Anatomic Alterations After Photodynamic Therapy for Chronic Central Serous Chorioretinopathy: A Multicenter Study
Claudio Iovino, Adrian Au, Jay Chhablani, et al.
Scientific Reports
|
October 3, 2024
Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy
Cansu de Muijnck, Lonneke Haer-Wigman, Judith A M van Everdingen, et al.
Journal of Inherited Metabolic Disease
|
January 6, 2025
Novel Insights Into Gyrate Atrophy of the Choroid and Retina (GACR): A Cohort Study
Berith M Balfoort, Filip Van den Broeck, Camiel J F Boon, et al.
JAMA Ophthalmology
|
October 15, 2020
Clinical Phenotype and Course of PDE6A-Associated Retinitis Pigmentosa Disease, Characterized in Preparation for a Gene Supplementation Trial
Laura Kuehlewein, Ditta Zobor, Sten Olof Andreasson, et al.
Acta Ophthalmologica
|
April 7, 2022
Clinical impact of the worldwide shortage of verteporfin (Visudyne®) on ophthalmic care
Marc J Sirks, Elon H C van Dijk, Noa Rosenberg, et al.
Progress in Retinal and Eye Research
|
July 19, 2019
Central serous chorioretinopathy: Towards an evidence-based treatment guideline
Thomas J van Rijssen, Elon H C van Dijk, Suzanne Yzer, et al.
Investigative Ophthalmology & Visual Science
|
August 15, 2018
The Spectrum of Structural and Functional Abnormalities in Female Carriers of Pathogenic Variants in the RPGR Gene
Mays Talib, Mary J van Schooneveld, Caroline Van Cauwenbergh, et al.
American Journal of Ophthalmology
|
July 28, 2021
CRB1-Associated Retinal Dystrophies: A Prospective Natural History Study in Anticipation of Future Clinical Trials
Xuan-Thanh-An Nguyen, Mays Talib, Mary J van Schooneveld, et al.
Investigative Ophthalmology & Visual Science
|
July 5, 2018
The Common ABCA4 Variant p.Asn1868Ile Shows Nonpenetrance and Variable Expression of Stargardt Disease When Present in trans With Severe Variants
Esmee H Runhart, Riccardo Sangermano, Stéphanie S Cornelis, et al.
Ophthalmology
|
January 24, 2012
Clinical course, genetic etiology, and visual outcome in cone and cone-rod dystrophy
Alberta A H J Thiadens, T My Lan Phan, Renate C Zekveld-Vroon, et al.
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of 30
Search research articles
Search
Showing results (261-270 of 293) with videos related to
Sort By:
Page
of 30
American Journal of Ophthalmology
|
May 4, 2020
Choroidal Anatomic Alterations After Photodynamic Therapy for Chronic Central Serous Chorioretinopathy: A Multicenter Study
Claudio Iovino, Adrian Au, Jay Chhablani, et al.
Scientific Reports
|
October 3, 2024
Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy
Cansu de Muijnck, Lonneke Haer-Wigman, Judith A M van Everdingen, et al.
Journal of Inherited Metabolic Disease
|
January 6, 2025
Novel Insights Into Gyrate Atrophy of the Choroid and Retina (GACR): A Cohort Study
Berith M Balfoort, Filip Van den Broeck, Camiel J F Boon, et al.
JAMA Ophthalmology
|
October 15, 2020
Clinical Phenotype and Course of PDE6A-Associated Retinitis Pigmentosa Disease, Characterized in Preparation for a Gene Supplementation Trial
Laura Kuehlewein, Ditta Zobor, Sten Olof Andreasson, et al.
Acta Ophthalmologica
|
April 7, 2022
Clinical impact of the worldwide shortage of verteporfin (Visudyne®) on ophthalmic care
Marc J Sirks, Elon H C van Dijk, Noa Rosenberg, et al.
Progress in Retinal and Eye Research
|
July 19, 2019
Central serous chorioretinopathy: Towards an evidence-based treatment guideline
Thomas J van Rijssen, Elon H C van Dijk, Suzanne Yzer, et al.
Investigative Ophthalmology & Visual Science
|
August 15, 2018
The Spectrum of Structural and Functional Abnormalities in Female Carriers of Pathogenic Variants in the RPGR Gene
Mays Talib, Mary J van Schooneveld, Caroline Van Cauwenbergh, et al.
American Journal of Ophthalmology
|
July 28, 2021
CRB1-Associated Retinal Dystrophies: A Prospective Natural History Study in Anticipation of Future Clinical Trials
Xuan-Thanh-An Nguyen, Mays Talib, Mary J van Schooneveld, et al.
Investigative Ophthalmology & Visual Science
|
July 5, 2018
The Common ABCA4 Variant p.Asn1868Ile Shows Nonpenetrance and Variable Expression of Stargardt Disease When Present in trans With Severe Variants
Esmee H Runhart, Riccardo Sangermano, Stéphanie S Cornelis, et al.
Ophthalmology
|
January 24, 2012
Clinical course, genetic etiology, and visual outcome in cone and cone-rod dystrophy
Alberta A H J Thiadens, T My Lan Phan, Renate C Zekveld-Vroon, et al.
Page
of 30