Omar AR Mahroo, M.D., Ph.D.

University of Cambridge, Cambridge, England, United Kingdom 
"Omar Mahroo"
Mean distance: 16.1 (cluster 11)
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Jiang X, Mahroo OA. (2022) Human retinal dark adaptation tracked in vivo with the electroretinogram: insights into processes underlying recovery of cone- and rod-mediated vision. The Journal of Physiology
De Silva SR, Arno G, Robson AG, et al. (2020) The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapies. Progress in Retinal and Eye Research. 100898
Khan KN, Borooah S, Lando L, et al. (2020) Quantifying the Separation Between the Retinal Pigment Epithelium and Bruch's Membrane using Optical Coherence Tomography in Patients with Inherited Macular Degeneration. Translational Vision Science & Technology. 9: 26
Schiff ER, Varela MD, Robson AG, et al. (2020) A genetic and clinical study of individuals with nonsyndromic retinopathy consequent upon sequence variants in HGSNAT, the gene associated with Sanfilippo C mucopolysaccharidosis. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
Pontikos N, Arno G, Jurkute N, et al. (2020) Genetic Basis of Inherited Retinal Disease in a Molecularly Characterized Cohort of More Than 3000 Families from the United Kingdom. Ophthalmology
Brigell M, Jeffrey BG, Mahroo OA, et al. (2020) ISCEV extended protocol for derivation and analysis of the strong flash rod-isolated ERG a-wave. Documenta Ophthalmologica. Advances in Ophthalmology
Afshar F, Arno G, Ba-Abbad R, et al. (2019) Awareness of olfactory impairment in a cohort of patients with CNGB1-associated retinitis pigmentosa. Eye (London, England)
Pekacka A, Hobby A, Chow I, et al. (2019) Comparison of peak times of photopic flicker electroretinogram responses recorded using conventional and portable systems in Birdshot chorioretinopathy Acta Ophthalmologica. 97
Lim WS, Magan T, Mahroo OA, et al. (2018) Retinal thickness measurements in sickle cell patients with HbSS and HbSC genotype. Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie. 53: 420-424
Mahroo OA, Fujinami K, Moore AT, et al. (2018) Retinal findings in a patient with mutations in ABCC6 and ABCA4. Eye (London, England)
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