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Ophthalmic Plastic and Reconstructive Surgery
|
July 12, 2011
Endoscopic endonasal retrieval of a nasolacrimal duct stone via the valve of Hasner in the inferior meatus
Ran Ben Cnaan, Mariya Moosajee, Catherine J Heatley, et al.
Genes
|
February 24, 2024
Inherited Optic Neuropathies: Real-World Experience in the Paediatric Neuro-Ophthalmology Clinic
Michael James Gilhooley, Naz Raoof, Patrick Yu-Wai-Man, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 20, 2023
Successful large gene augmentation of USH2A with non-viral episomal vectors
Maria Toms, Lyes Toualbi, Patrick V Almeida, et al.
Research Involvement and Engagement
|
November 3, 2018
Overcoming barriers to the involvement of deafblind people in conversations about research: recommendations from individuals with Usher syndrome
Andrew Skilton, Emma Boswell, Kevin Prince, et al.
Genes
|
January 27, 2021
From Transcriptomics to Treatment in Inherited Optic Neuropathies
Michael James Gilhooley, Nicholas Owen, Mariya Moosajee, et al.
Healthcare (Basel, Switzerland)
|
January 8, 2025
User-Centred Design and Development of a Smartphone Application (<i>OverSight</i>) for Digital Phenotyping in Ophthalmology
Kishan Devraj, Lee Jones, Bethany Higgins, et al.
Ophthalmic Surgery, Lasers & Imaging Retina
|
September 14, 2017
Quantitative and Qualitative Features of Spectral-Domain Optical Coherence Tomography Provide Prognostic Indicators for Visual Acuity in Patients With Choroideremia
Alessandro Abbouda, Wei Sing Lim, Lina Sprogyte, et al.
NPJ Digital Medicine
|
May 29, 2026
Feasibility of smartphone-based digital phenotyping to measure visual function and mental health outcomes in patients with inherited retinal diseases
Lee Jones, Bethany Higgins, Kishan Devraj, et al.
Experimental Eye Research
|
January 10, 2017
Mechanism and evidence of nonsense suppression therapy for genetic eye disorders
Rose Richardson, Matthew Smart, Dhani Tracey-White, et al.
Genes
|
June 27, 2024
Identification of a Novel Frameshift Variant in <i>MYF5</i> Leading to External Ophthalmoplegia with Rib and Vertebral Anomalies
Paulina Ocieczek, Ngozi Oluonye, Cécile Méjécase, et al.
Page
of 18
Search research articles
Search
Showing results (71-80 of 176) with videos related to
Sort By:
Page
of 18
Ophthalmic Plastic and Reconstructive Surgery
|
July 12, 2011
Endoscopic endonasal retrieval of a nasolacrimal duct stone via the valve of Hasner in the inferior meatus
Ran Ben Cnaan, Mariya Moosajee, Catherine J Heatley, et al.
Genes
|
February 24, 2024
Inherited Optic Neuropathies: Real-World Experience in the Paediatric Neuro-Ophthalmology Clinic
Michael James Gilhooley, Naz Raoof, Patrick Yu-Wai-Man, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 20, 2023
Successful large gene augmentation of USH2A with non-viral episomal vectors
Maria Toms, Lyes Toualbi, Patrick V Almeida, et al.
Research Involvement and Engagement
|
November 3, 2018
Overcoming barriers to the involvement of deafblind people in conversations about research: recommendations from individuals with Usher syndrome
Andrew Skilton, Emma Boswell, Kevin Prince, et al.
Genes
|
January 27, 2021
From Transcriptomics to Treatment in Inherited Optic Neuropathies
Michael James Gilhooley, Nicholas Owen, Mariya Moosajee, et al.
Healthcare (Basel, Switzerland)
|
January 8, 2025
User-Centred Design and Development of a Smartphone Application (<i>OverSight</i>) for Digital Phenotyping in Ophthalmology
Kishan Devraj, Lee Jones, Bethany Higgins, et al.
Ophthalmic Surgery, Lasers & Imaging Retina
|
September 14, 2017
Quantitative and Qualitative Features of Spectral-Domain Optical Coherence Tomography Provide Prognostic Indicators for Visual Acuity in Patients With Choroideremia
Alessandro Abbouda, Wei Sing Lim, Lina Sprogyte, et al.
NPJ Digital Medicine
|
May 29, 2026
Feasibility of smartphone-based digital phenotyping to measure visual function and mental health outcomes in patients with inherited retinal diseases
Lee Jones, Bethany Higgins, Kishan Devraj, et al.
Experimental Eye Research
|
January 10, 2017
Mechanism and evidence of nonsense suppression therapy for genetic eye disorders
Rose Richardson, Matthew Smart, Dhani Tracey-White, et al.
Genes
|
June 27, 2024
Identification of a Novel Frameshift Variant in <i>MYF5</i> Leading to External Ophthalmoplegia with Rib and Vertebral Anomalies
Paulina Ocieczek, Ngozi Oluonye, Cécile Méjécase, et al.
Page
of 18