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Mervyn G Thomas

Showing results (51-60 of 74) with videos related to

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Nature Communications|August 8, 2024
Single cell dual-omic atlas of the human developing retinaZhen Zuo, Xuesen Cheng, Salma Ferdous, et al.
International Journal of Molecular Sciences|April 3, 2021
Optic Nerve Head and Retinal Abnormalities Associated with Congenital Fibrosis of the Extraocular MusclesMervyn G Thomas, Gail D E Maconachie, Helen J Kuht, et al.
European Journal of Ophthalmology|November 20, 2020
Impact of COVID-19 pandemic and lockdown on eye emergenciesAlicia Poyser, Sundeep S Deol, Lina Osman, et al.
Ophthalmic Genetics|June 16, 2021
Diagnostic yield of targeted next-generation sequencing in infantile nystagmus syndromeJae-Hwan Choi, Su-Jin Kim, Mervyn G Thomas, et al.
Eye (London, England)|January 13, 2022
Feasibility and clinical utility of handheld fundus cameras for retinal imagingSusmit Das, Helen J Kuht, Ian De Silva, et al.
Eye (London, England)|May 25, 2022
Correction: Feasibility and clinical utility of handheld fundus cameras for retinal imagingSusmit Das, Helen J Kuht, Ian De Silva, et al.
Human Molecular Genetics|August 4, 2020
SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specializationHelen J Kuht, Jinu Han, Gail D E Maconachie, et al.
American Journal of Ophthalmology|August 29, 2024
Optic Nerve Head Morphological Variation in Craniosynostosis: A Cohort StudySohaib R Rufai, Mervyn G Thomas, Oliver R Marmoy, et al.
Brain Communications|March 13, 2026
<i>CACNB3</i> defects are associated with infantile idiopathic nystagmusChristoph Jüschke, Kira Linsel, Marta Owczarek-Lipska, et al.
Brain : a Journal of Neurology|April 23, 2019
Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmusAnja K Mayer, Muhammad Mahajnah, Mervyn G Thomas, et al.
Pageof 8

Showing results (51-60 of 74) with videos related to

Sort By:
Pageof 8
Nature Communications|August 8, 2024
Single cell dual-omic atlas of the human developing retinaZhen Zuo, Xuesen Cheng, Salma Ferdous, et al.
International Journal of Molecular Sciences|April 3, 2021
Optic Nerve Head and Retinal Abnormalities Associated with Congenital Fibrosis of the Extraocular MusclesMervyn G Thomas, Gail D E Maconachie, Helen J Kuht, et al.
European Journal of Ophthalmology|November 20, 2020
Impact of COVID-19 pandemic and lockdown on eye emergenciesAlicia Poyser, Sundeep S Deol, Lina Osman, et al.
Ophthalmic Genetics|June 16, 2021
Diagnostic yield of targeted next-generation sequencing in infantile nystagmus syndromeJae-Hwan Choi, Su-Jin Kim, Mervyn G Thomas, et al.
Eye (London, England)|January 13, 2022
Feasibility and clinical utility of handheld fundus cameras for retinal imagingSusmit Das, Helen J Kuht, Ian De Silva, et al.
Eye (London, England)|May 25, 2022
Correction: Feasibility and clinical utility of handheld fundus cameras for retinal imagingSusmit Das, Helen J Kuht, Ian De Silva, et al.
Human Molecular Genetics|August 4, 2020
SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specializationHelen J Kuht, Jinu Han, Gail D E Maconachie, et al.
American Journal of Ophthalmology|August 29, 2024
Optic Nerve Head Morphological Variation in Craniosynostosis: A Cohort StudySohaib R Rufai, Mervyn G Thomas, Oliver R Marmoy, et al.
Brain Communications|March 13, 2026
<i>CACNB3</i> defects are associated with infantile idiopathic nystagmusChristoph Jüschke, Kira Linsel, Marta Owczarek-Lipska, et al.
Brain : a Journal of Neurology|April 23, 2019
Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmusAnja K Mayer, Muhammad Mahajnah, Mervyn G Thomas, et al.
Pageof 8