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The Journal of Clinical Investigation
|
May 25, 2011
The human visual cortex responds to gene therapy-mediated recovery of retinal function
Manzar Ashtari, Laura L Cyckowski, Justin F Monroe, et al.
Clinical Ophthalmology (Auckland, N.Z.)
|
March 10, 2021
A Virtual Reality Orientation and Mobility Test for Inherited Retinal Degenerations: Testing a Proof-of-Concept After Gene Therapy
Tomas S Aleman, Alexander J Miller, Katherine H Maguire, et al.
Ophthalmology
|
April 2, 2021
Durability of Voretigene Neparvovec for Biallelic RPE65-Mediated Inherited Retinal Disease: Phase 3 Results at 3 and 4 Years
Albert M Maguire, Stephen Russell, Daniel C Chung, et al.
Molecular Vision
|
April 3, 2010
A detailed phenotypic assessment of individuals affected by MFRP-related oculopathy
Rajarshi Mukhopadhyay, Panagiotis I Sergouniotis, Donna S Mackay, et al.
Clinical Genetics
|
November 14, 2019
Functional characterization of novel MFSD8 pathogenic variants anticipates neurological involvement in juvenile isolated maculopathy
Miriam Bauwens, Stephan Storch, Nicole Weisschuh, et al.
Revue Neurologique
|
July 23, 2004
[Congenital myasthenic syndromes due to mutations in the rapsyn gene]
B Eymard, C Ioos, A Barois, et al.
The Journal of Investigative Dermatology
|
November 18, 2006
Pseudoxanthoma elasticum-like phenotype with cutis laxa and multiple coagulation factor deficiency represents a separate genetic entity
Olivier M Vanakker, Ludovic Martin, Dealba Gheduzzi, et al.
Experimental Eye Research
|
September 25, 2021
Broad locations of antigenic regions for anti-TRPM1 autoantibodies in paraneoplastic retinopathy with retinal ON bipolar cell dysfunction
Daichi Gyoten, Shinji Ueno, Satoshi Okado, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 9, 2016
arrEYE: a customized platform for high-resolution copy number analysis of coding and noncoding regions of known and candidate retinal dystrophy genes and retinal noncoding RNAs
Caroline Van Cauwenbergh, Kristof Van Schil, Robrecht Cannoodt, et al.
Investigative Ophthalmology & Visual Science
|
April 28, 2025
Progression of Atrophy as a Function of ABCA4 Variants and Age of Onset in Stargardt Disease
Jeroen A A H Pas, Catherina H Z Li, Filip Van den Broeck, et al.
Page
of 44
Search research articles
Search
Showing results (311-320 of 438) with videos related to
Sort By:
Page
of 44
The Journal of Clinical Investigation
|
May 25, 2011
The human visual cortex responds to gene therapy-mediated recovery of retinal function
Manzar Ashtari, Laura L Cyckowski, Justin F Monroe, et al.
Clinical Ophthalmology (Auckland, N.Z.)
|
March 10, 2021
A Virtual Reality Orientation and Mobility Test for Inherited Retinal Degenerations: Testing a Proof-of-Concept After Gene Therapy
Tomas S Aleman, Alexander J Miller, Katherine H Maguire, et al.
Ophthalmology
|
April 2, 2021
Durability of Voretigene Neparvovec for Biallelic RPE65-Mediated Inherited Retinal Disease: Phase 3 Results at 3 and 4 Years
Albert M Maguire, Stephen Russell, Daniel C Chung, et al.
Molecular Vision
|
April 3, 2010
A detailed phenotypic assessment of individuals affected by MFRP-related oculopathy
Rajarshi Mukhopadhyay, Panagiotis I Sergouniotis, Donna S Mackay, et al.
Clinical Genetics
|
November 14, 2019
Functional characterization of novel MFSD8 pathogenic variants anticipates neurological involvement in juvenile isolated maculopathy
Miriam Bauwens, Stephan Storch, Nicole Weisschuh, et al.
Revue Neurologique
|
July 23, 2004
[Congenital myasthenic syndromes due to mutations in the rapsyn gene]
B Eymard, C Ioos, A Barois, et al.
The Journal of Investigative Dermatology
|
November 18, 2006
Pseudoxanthoma elasticum-like phenotype with cutis laxa and multiple coagulation factor deficiency represents a separate genetic entity
Olivier M Vanakker, Ludovic Martin, Dealba Gheduzzi, et al.
Experimental Eye Research
|
September 25, 2021
Broad locations of antigenic regions for anti-TRPM1 autoantibodies in paraneoplastic retinopathy with retinal ON bipolar cell dysfunction
Daichi Gyoten, Shinji Ueno, Satoshi Okado, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 9, 2016
arrEYE: a customized platform for high-resolution copy number analysis of coding and noncoding regions of known and candidate retinal dystrophy genes and retinal noncoding RNAs
Caroline Van Cauwenbergh, Kristof Van Schil, Robrecht Cannoodt, et al.
Investigative Ophthalmology & Visual Science
|
April 28, 2025
Progression of Atrophy as a Function of ABCA4 Variants and Age of Onset in Stargardt Disease
Jeroen A A H Pas, Catherina H Z Li, Filip Van den Broeck, et al.
Page
of 44