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Page 1
Identification and characterisation of a rare MTTP variant underlying hereditary non-alcoholic fatty liver disease.
Grove JI, Lo PCK, Shrine N, Barwell J, Wain LV, Tobin MD, Salter AM, Borkar AN, Cuevas-Ocaña S, Bennett N, John C, Ntalla I, Jones GE, Neal CP, Thomas MG, Kuht H, Gupta P, Vemala VM, Grant A, Adewoye AB, Shenoy KT, Balakumaran LK, Hollox EJ, Hannan NRF, Aithal GP. Grove JI, et al. Among authors: thomas mg. JHEP Rep. 2023 Apr 23;5(8):100764. doi: 10.1016/j.jhepr.2023.100764. eCollection 2023 Aug. JHEP Rep. 2023. PMID: 37484212 Free PMC article.
Congenital monocular elevation deficiency associated with a novel TUBB3 gene variant.
Thomas MG, Maconachie GDE, Constantinescu CS, Chan WM, Barry B, Hisaund M, Sheth V, Kuht HJ, Dineen RA, Harieaswar S, Engle EC, Gottlob I. Thomas MG, et al. Br J Ophthalmol. 2020 Apr;104(4):547-550. doi: 10.1136/bjophthalmol-2019-314293. Epub 2019 Jul 13. Br J Ophthalmol. 2020. PMID: 31302631 Free PMC article.
Impact of COVID-19 pandemic and lockdown on retinal detachments.
Poyser A, Deol SS, Osman L, Sivagnanasithiyar T, Kuht HJ, Manrique R, Okafor LO, Sharpe D, Savant V, Sarodia U, Sarvananthan N, Chaudhuri R, Banerjee S, Burns J, Thomas MG. Poyser A, et al. Among authors: thomas mg. Eye (Lond). 2021 Aug;35(8):2322-2323. doi: 10.1038/s41433-020-01137-x. Epub 2020 Aug 18. Eye (Lond). 2021. PMID: 32811997 Free PMC article. No abstract available.
Current and emerging treatments for albinism.
Liu S, Kuht HJ, Moon EH, Maconachie GDE, Thomas MG. Liu S, et al. Among authors: thomas mg. Surv Ophthalmol. 2021 Mar-Apr;66(2):362-377. doi: 10.1016/j.survophthal.2020.10.007. Epub 2020 Oct 29. Surv Ophthalmol. 2021. PMID: 33129801 Review.
Normal and abnormal foveal development.
Thomas MG, Papageorgiou E, Kuht HJ, Gottlob I. Thomas MG, et al. Br J Ophthalmol. 2022 May;106(5):593-599. doi: 10.1136/bjophthalmol-2020-316348. Epub 2020 Nov 4. Br J Ophthalmol. 2022. PMID: 33148537 Review.
Impact of COVID-19 pandemic and lockdown on eye emergencies.
Poyser A, Deol SS, Osman L, Kuht HJ, Sivagnanasithiyar T, Manrique R, Okafor LO, DeSilva I, Sharpe D, Savant V, Sarodia U, Sarvananthan N, Chaudhuri R, Banerjee S, Burns J, Thomas MG. Poyser A, et al. Among authors: thomas mg. Eur J Ophthalmol. 2021 Nov;31(6):2894-2900. doi: 10.1177/1120672120974944. Epub 2020 Nov 19. Eur J Ophthalmol. 2021. PMID: 33213198 Free PMC article.
Discordant phenotypes in twins with infantile nystagmus.
Aamir A, Kuht HJ, McLean RJ, Maconachie GDE, Sheth V, Dawar B, Purohit R, Sylvius N, Hisaund M, Zubcov-Iwantscheff A, Proudlock FA, Gottlob I, Thomas MG. Aamir A, et al. Among authors: thomas mg. Sci Rep. 2021 Feb 2;11(1):2826. doi: 10.1038/s41598-021-82368-0. Sci Rep. 2021. PMID: 33531592 Free PMC article.
Clinical utility gene card for FRMD7-related infantile nystagmus.
Dawar B, Kuht HJ, Han J, Maconachie GDE, Thomas MG. Dawar B, et al. Among authors: thomas mg. Eur J Hum Genet. 2021 Oct;29(10):1584-1588. doi: 10.1038/s41431-021-00826-9. Epub 2021 Feb 25. Eur J Hum Genet. 2021. PMID: 33633368 Free PMC article. No abstract available.
638 results