Publications by authors named "Fatima Shawkat"

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A Rare Case of CLN3-associated Isolated Retinal Degeneration with Macular Oedema.
Dimitrios Kalogeropoulos, Samir Khandhadia, Fatima Shawkat, Andrew John Lotery

Klin Monbl Augenheilkd· November 2025

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Diagnosis and treatment of autoimmune retinopathy: review of current approaches.
Dimitrios Kalogeropoulos, Andrew John Lotery, Carlos Pavesio, Chris Kalogeropoulos, Panagiotis Kanavaros, Fatima Shawkat

Int Ophthalmol· August 2025

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Can a Portable Flash Visual Evoked Potential (VEP) Device Identify Chiasmal Decussation Anomalies in Albinism?
Eloise Keeling, Perry Carter, Abdi Malik Musa, Fatima Shawkat, Helena Lee

Diagnostics (Basel)· May 2025

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Could a hand-held, visual electrophysiology device theoretically reduce diagnostic waiting times for complex eye conditions in the NHS? A Discrete Event Simulation (DES) modelling study.
Steffen Bayer, Daniel Garillo, Marion Penn, Maria Chorozoglou, Sally Brailsford, Fatima Shawkat

BMC Health Serv Res· March 2025

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Crocodile Skin Retinal Appearance: Miliary Distribution of Bilateral Idiopathic Multifocal Retinal Pigment Epithelial Detachments.
Alexandros Chatzirallis, Dimitrios Kalogeropoulos, Fatima Shawkat, Anna M Roszkowska, Rino Frisina

Ophthalmic Surg Lasers Imaging Retina· February 2025

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Eyetracking-enhanced VEP for nystagmus.
Matt J Dunn, Perry Carter, Jay Self, Helena Lee, Fatima Shawkat

Sci Rep· December 2023

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Correction: Comparison of the handheld RETeval ERG system with a routine ERG system in healthy adults and in paediatric patients.
Perry Carter, Arabella Gordon-Reid, Fatima Shawkat, Jay E Self

Eye (Lond)· October 2021

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Comparison of the handheld RETeval ERG system with a routine ERG system in healthy adults and in paediatric patients.
Perry Carter, Arabella Gordon-Reid, Fatima Shawkat, Jay E Self

Eye (Lond)· August 2021

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A small gene sequencing panel realises a high diagnostic rate in patients with congenital nystagmus following basic phenotyping.
Luke O'Gorman, Chelsea S Norman, Luke Michaels, Tutte Newall, Andrew H Crosby, Fatima Shawkat

Sci Rep· September 2019

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Long term follow-up of a family with dominant cone dystrophy.
Georgios Tsokolas, Hussein Almuhtaseb, Helen Griffiths, Fatima Shawkat, Reuben J Pengelly

Int J Ophthalmol· December 2018

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Retinitis pigmentosa and bilateral cystoid macular oedema in a patient heterozygous for the RIM1 mutation previously associated with cone-rod dystrophy 7.
Alasdair N Warwick, Fatima Shawkat, Andrew J Lotery

Ophthalmic Genet· November 2017

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Identification of a functionally significant tri-allelic genotype in the Tyrosinase gene (TYR) causing hypomorphic oculocutaneous albinism (OCA1B).
Chelsea S Norman, Luke O'Gorman, Jane Gibson, Reuben J Pengelly, Diana Baralle, Fatima Shawkat

Sci Rep· June 2017

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Common spectral domain OCT and electrophysiological findings in different pattern dystrophies.
Shabeeba Rashed Hannan, Gabriella de Salvo, Alina Stinghe, Fatima Shawkat, Andrew J Lotery

Br J Ophthalmol· May 2013

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Allelic variation of the FRMD7 gene in congenital idiopathic nystagmus.
James E Self, Fatima Shawkat, Crispin T Malpas, N Simon Thomas, Christopher M Harris

Arch Ophthalmol· September 2007

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Fine mapping of the X-linked recessive congenital idiopathic nystagmus locus at Xq24-q26.3.
James Edward Self, Sarah Ennis, Andrew Collins, Fatima Shawkat, Christopher Mark Harris

Mol Vis· October 2006

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Joubert syndrome: long-term follow-up.
Peter R Hodgkins, Christopher M Harris, Fatima S Shawkat, Dorothy A Thompson, Kling Chong

Dev Med Child Neurol· October 2004

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