Publications

Moradi Publications
 

An eye surgeon can write new reports or original eye research, known as publications, to inform other eye surgeons and eye professionals. This advances the science and practice of eye care, or ophthalmology. These publications are in the peer reviewed medical literature, written by Mr Moradi with his co-authors.


Comment on: 'Patients with unexplained neurological symptoms and signs should be screened for vitamin B12 deficiency regardless of haemoglobin levels'.

Bobat H, Akyol M, Moradi P. Eye (Lond). 2023 Jan;37(1):191-192.

doi: 10.1038/s41433-022-02162-8. PMID: 35780189

Emergency eye colour change.

Bobat H, Lochhead J, Moradi P. Emerg Med J. 2022 Feb;39(2):123-131. doi: 10.1136/emermed-2021-211834. PMID: 35058290.


Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies.

Sheck L, Davies WL, Moradi P, Robson AG, Kumaran N, Liasis AC, Webster AR, Moore AT, Michaelides M.Ophthalmology. 2018 Jun;125(6):894-903. doi: 10.1016/j.ophtha.2017.12.013. Epub 2018 Feb 3.PMID: 29398085


Sudden pseudoproptosis.

Moradi P, Krishnanandan S, Verity D.Emerg Med J. 2014 Aug;31(8):624. doi: 10.1136/emermed-2013-203249. Epub 2013 Oct 17.PMID: 24136120


Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic study.

Dev Borman A, Ocaka LA, Mackay DS, Ripamonti C, Henderson RH, Moradi P, Hall G, Black GC, Robson AG, Holder GE, Webster AR, Fitzke F, Stockman A, Moore AT.Invest Ophthalmol Vis Sci. 2012 Jun 22;53(7):3927-38. doi: 10.1167/iovs.12-9548.PMID: 22570351



Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy.

Tan MH, Mackay DS, Cowing J, Tran HV, Smith AJ, Wright GA, Dev-Borman A, Henderson RH, Moradi P, Russell-Eggitt I, MacLaren RE, Robson AG, Cheetham ME, Thompson DA, Webster AR, Michaelides M, Ali RR, Moore AT.PLoS One. 2012;7(3):e32330. doi: 10.1371/journal.pone.0032330. Epub 2012 Mar 6.PMID: 22412862



Epibulbar molluscum contagiosum lesions in multiple myeloma.

Moradi P, Bhogal M, Thaung C, Dart J.Cornea. 2011 Aug;30(8):910-1. doi: 10.1097/ICO.0b013e3181f234bf. PMID: 21448067



Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations.

Mackay DS, Ocaka LA, Borman AD, Sergouniotis PI, Henderson RH, Moradi P, Robson AG, Thompson DA, Webster AR, Moore AT.Invest Ophthalmol Vis Sci. 2011 May 9;52(6):3032-8. doi: 10.1167/iovs.10-7025.PMID: 21310915



RDH12 retinopathy: novel mutations and phenotypic description.

Mackay DS, Dev Borman A, Moradi P, Henderson RH, Li Z, Wright GA, Waseem N, Gandra M, Thompson DA, Bhattacharya SS, Holder GE, Webster AR, Moore AT. Mol Vis. 2011;17:2706-16. Epub 2011 Oct 19. PMID: 22065924



Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.

Henderson RH, Mackay DS, Li Z, Moradi P, Sergouniotis P, Russell-Eggitt I, Thompson DA, Robson AG, Holder GE, Webster AR, Moore AT.Br J Ophthalmol. 2011 Jun;95(6):811-7. doi: 10.1136/bjo.2010.186882. Epub 2010 Oct 17. PMID: 20956273



Focus on molecules: centrosomal protein 290 (CEP290).

Moradi P, Davies WL, Mackay DS, Cheetham ME, Moore AT.Exp Eye Res. 2011 May;92(5):316-7. doi: 10.1016/j.exer.2010.05.009. Epub 2010 May 20.PMID: 20493186



 Novel mutations in MERTK associated with childhood onset rod-cone dystrophy.

Mackay DS, Henderson RH, Sergouniotis PI, Li Z, Moradi P, Holder GE, Waseem N, Bhattacharya SS, Aldahmesh MA, Alkuraya FS, Meyer B, Webster AR, Moore AT.Mol Vis. 2010 Mar 9;16:369-77.PMID: 20300561 



Mutational analysis of patients with early onset retinal dystrophies

Mackay DS, Moradi P, Henderson RHH, Webster RA, Moore AT Journal of Medical Genetics September 2007. Conference: British Human Genetics Conference. Volume 44.



Emergency retinal pallor.

Moradi P, Chandra A, Islam N.Emerg Med J. 2010 Mar;27(3):198. doi: 10.1136/emj.2009.073320. PMID: 20304884



Eye drop compliance in religious fasting.

Moradi P. Ophthalmology. 2008 Aug;115(8):1440; author reply 1440-1. doi: 10.1016/j.ophtha.2008.05.011. PMID: 18675710



Focus on molecules: retinol dehydrogenase 12 (RDH12).

Moradi P, Mackay D, Hunt DM, Moore AT.Exp Eye Res. 2008 Sep;87(3):160-1. doi: 10.1016/j.exer.2008.05.013. Epub 2008 Jul 2. PMID: 18599039



Electrophysiological monitoring in a patient with an optic nerve glioma.

Moradi P, Robson AG, Rose GE, Holder GE.Doc Ophthalmol. 2008 Sep;117(2):171-4. doi: 10.1007/s10633-008-9118-9. Epub 2008 Feb 27. PMID: 18301934



Molecular genetics of infantile-onset retinal dystrophies.

Moradi P, Moore AT. Eye (Lond). 2007 Oct;21(10):1344-51. doi: 10.1038/sj.eye.6702843. PMID: 17914438



Technical note: the effect of refractive blur on colour vision evaluated using the Cambridge Colour Test, the Ishihara Pseudoisochromatic Plates and the Farnsworth Munsell 100 Hue Test.

Thyagarajan S, Moradi P, Membrey L, Alistair D, Laidlaw H. Ophthalmic Physiol Opt. 2007 May;27(3):315-9. doi: 10.1111/j.1475-1313.2007.00469.x. PMID: 17470246



Teenagers' perceptions of blindness related to smoking: a novel message to a vulnerable group.

Moradi P, Thornton J, Edwards R, Harrison RA, Washington SJ, Kelly SP.Br J Ophthalmol. 2007 May;91(5):605-7. doi: 10.1136/bjo.2006.108191. Epub 2007 Feb 6. PMID: 17284473



Report of a novel lobular chorioretinal dystrophy.

Moradi P, Lotery A.Eye (Lond). 2006 Dec;20(12):1390-2. doi: 10.1038/sj.eye.6702233. Epub 2006 Feb 3. PMID: 16456598



HACEK endocarditis causing endogenous endophthalmitis and a metastatic abscess.

Moradi P, Roberton B, Osborne R, Muhtaseb M, Graham EM, Klein J, Stanford MR.Eye (Lond). 2006 Feb;20(2):254-5. doi: 10.1038/sj.eye.6701832. PMID: 15688044



Can patients self-assess their requirement for cataract surgery?

Moradi P, Shute N, Whitefield L.J Cataract Refract Surg. 2006 Apr;32(4):692. doi: 10.1016/j.jcrs.2006.01.043.PMID: 16698501



Degree, duration, and causes of visual loss in uveitis.

Durrani OM, Tehrani NN, Marr JE, Moradi P, Stavrou P, Murray PI.Br J Ophthalmol. 2004 Sep;88(9):1159-62. doi: 10.1136/bjo.2003.037226. PMID: 15317708



Whither hospital linen? Two centre observational study of alien hospital linen.

Moradi P, Rowe J, Washington S.BMJ. 1999 Dec 18-25;319(7225):1614. doi: 10.1136/bmj.319.7225.1614. PMID: 10600962 



 Immunodetection of 11 beta-hydroxysteroid dehydrogenase type 2 in human mineralocorticoid target tissues: evidence for nuclear localization.Shimojo M, Ricketts ML, Petrelli MD, Moradi P, Johnson GD, Bradwell AR, Hewison M, Howie AJ, Stewart PM.Endocrinology. 1997 Mar;138(3):1305-11. doi: 10.1210/endo.138.3.4994. PMID: 9048640