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Medrxiv : the Preprint Server for Health Sciences
|
June 30, 2025
Genome-Wide Insights into the Genes and Pathways Shaping Human Foveal Development
Callum Hunt, Ha-Jun Yoon, Alvin Lirio, et al.
Eye (London, England)
|
November 30, 2021
Patterns of attendances to the hospital emergency eye care service: a multicentre study in England
Ian De Silva, Mervyn G Thomas, Amy-Lee Shirodkar, et al.
Scientific Reports
|
July 10, 2025
Identifying biomarkers for papilledema and pseudopapilledema
Rishi Sekhri, Helen J Kuht, Zhanhan Tu, et al.
Scientific Reports
|
April 14, 2026
Artificial intelligence-driven virtual reality eye-tracking for the objective measurement of MRD1 and MRD2 in blepharoptosis
Reenette Savant, Swati Parida, Callum Hunt, et al.
Brain : a Journal of Neurology
|
February 10, 2011
The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus
Mervyn G Thomas, Moira Crosier, Susan Lindsay, et al.
Research Square
|
March 30, 2023
Eye movement defects in KO zebrafish reveals <i>SRPK3</i> as a causative gene for an X-linked intellectual disability
Yu-Ri Lee, Mervyn G Thomas, Arkaprava Roychaudhury, et al.
Diagnostics (Basel, Switzerland)
|
March 28, 2025
Foveal Hypoplasia Grading with Optical Coherence Tomography: Agreement and Challenges Across Experience Levels
Riddhi Shenoy, Gail D E Maconachie, Swati Parida, et al.
Investigative Ophthalmology & Visual Science
|
September 9, 2025
Genome-Wide Insights Into the Genes and Pathways Shaping Human Foveal Development: Redefining the Genetic Landscape of Foveal Hypoplasia
Callum Hunt, Ha-Jun Yoon, Alvin Lirio, et al.
Biorxiv : the Preprint Server for Biology
|
June 5, 2026
Targeting melanosome pH is an effective method for the treatment of oculocutaneous albinism
Samuel J Grondin, Daniela St Pierre, David J Green, et al.
JHEP Reports : Innovation in Hepatology
|
July 24, 2023
Identification and characterisation of a rare <i>MTTP</i> variant underlying hereditary non-alcoholic fatty liver disease
Jane I Grove, Peggy C K Lo, Nick Shrine, et al.
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of 8
Search research articles
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Showing results (61-70 of 74) with videos related to
Sort By:
Page
of 8
Medrxiv : the Preprint Server for Health Sciences
|
June 30, 2025
Genome-Wide Insights into the Genes and Pathways Shaping Human Foveal Development
Callum Hunt, Ha-Jun Yoon, Alvin Lirio, et al.
Eye (London, England)
|
November 30, 2021
Patterns of attendances to the hospital emergency eye care service: a multicentre study in England
Ian De Silva, Mervyn G Thomas, Amy-Lee Shirodkar, et al.
Scientific Reports
|
July 10, 2025
Identifying biomarkers for papilledema and pseudopapilledema
Rishi Sekhri, Helen J Kuht, Zhanhan Tu, et al.
Scientific Reports
|
April 14, 2026
Artificial intelligence-driven virtual reality eye-tracking for the objective measurement of MRD1 and MRD2 in blepharoptosis
Reenette Savant, Swati Parida, Callum Hunt, et al.
Brain : a Journal of Neurology
|
February 10, 2011
The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus
Mervyn G Thomas, Moira Crosier, Susan Lindsay, et al.
Research Square
|
March 30, 2023
Eye movement defects in KO zebrafish reveals <i>SRPK3</i> as a causative gene for an X-linked intellectual disability
Yu-Ri Lee, Mervyn G Thomas, Arkaprava Roychaudhury, et al.
Diagnostics (Basel, Switzerland)
|
March 28, 2025
Foveal Hypoplasia Grading with Optical Coherence Tomography: Agreement and Challenges Across Experience Levels
Riddhi Shenoy, Gail D E Maconachie, Swati Parida, et al.
Investigative Ophthalmology & Visual Science
|
September 9, 2025
Genome-Wide Insights Into the Genes and Pathways Shaping Human Foveal Development: Redefining the Genetic Landscape of Foveal Hypoplasia
Callum Hunt, Ha-Jun Yoon, Alvin Lirio, et al.
Biorxiv : the Preprint Server for Biology
|
June 5, 2026
Targeting melanosome pH is an effective method for the treatment of oculocutaneous albinism
Samuel J Grondin, Daniela St Pierre, David J Green, et al.
JHEP Reports : Innovation in Hepatology
|
July 24, 2023
Identification and characterisation of a rare <i>MTTP</i> variant underlying hereditary non-alcoholic fatty liver disease
Jane I Grove, Peggy C K Lo, Nick Shrine, et al.
Page
of 8