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Author Details
Full Name
Peter Charbel Issa
Affiliation
Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust
ORCID
Career Start Year
2000
Papers
205
H Index
46
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37739233
Developing a Continuous Severity Scale for Macular Telangiectasia Type 2 Using Deep Learning and Implications for Disease Grading.
Ophthalmology
2024
37806544
IMPG2-Related Maculopathy.
Am J Ophthalmol
2024
34670750
Inner retinal degeneration associated with optic nerve head drusen in pseudoxanthoma elasticum.
Br J Ophthalmol
2023
36592621
Current Management of Inherited Retinal Degeneration Patients in Europe: Results of a 2-Year Follow-Up Multinational Survey by the European Vision Institute Clinical Research Network - EVICR.net.
Ophthalmic Res
2023
36036427
MERTK missense variants in three patients with retinitis pigmentosa.
Ophthalmic Genet
2023
36260161
The retinal phenotype in primary hyperoxaluria type 2 and 3.
Pediatr Nephrol
2023
35948211
Tamoxifen Retinopathy and Macular Telangiectasia Type 2: Similarities and Differences on Multimodal Retinal Imaging.
Ophthalmol Retina
2023
34949787
Intravitreal injections as a leading cause of acute postoperative endophthalmitis-a regional survey in England.
Eye (Lond)
2023
32582926
Examination of the eye and retinal alterations in primary hyperoxaluria type 1.
Nephrol Dial Transplant
2022
36445968
Impaired glutamylation of RPGR<sup>ORF15</sup> underlies the cone-dominated phenotype associated with truncating distal ORF15 variants.
Proc Natl Acad Sci U S A
2022
36846105
Macular Telangiectasia Type 2: A Classification System Using MultiModal Imaging MacTel Project Report Number 10.
Ophthalmol Sci
2022
36314000
Novel imaging techniques for hydroxychloroquine retinopathy.
Front Med (Lausanne)
2022
33785507
North Carolina macular dystrophy shows a particular drusen phenotype and atrophy progression.
Br J Ophthalmol
2022
35066146
Retinal cadherins and the retinal cadherinopathies: Current concepts and future directions.
Prog Retin Eye Res
2022
35205358
<i>GUCY2D</i>-Related Retinal Dystrophy with Autosomal Dominant Inheritance-A Multicenter Case Series and Review of Reported Data.
Genes (Basel)
2022
34862446
The complexity of visual dysfunction in patients with pseudoxanthoma elasticum.
Eye (Lond)
2022
34673638
Structural Abnormalities of the Central Retina in Neurofibromatosis Type 2.
Ophthalmic Res
2022
34844251
Choriocapillaris Flow Signal Impairment in Sorsby Fundus Dystrophy.
Ophthalmologica
2022
34352251
Visual Dysfunction and Structural Correlates in Sorsby Fundus Dystrophy.
Am J Ophthalmol
2022
34167944
Morphological characteristics preceding exudative neovascularisation secondary to macular telangiectasia type 2.
Br J Ophthalmol
2022
34257060
Mitochondrial Retinopathy.
Ophthalmol Retina
2022
30808615
Right-angled vessels in macular telangiectasia type 2.
Br J Ophthalmol
2021
33549200
Retinopathy in McArdle Disease.
Ophthalmol Retina
2021
33784788
Diagnosis of Inherited Retinal Diseases.
Klin Monbl Augenheilkd
2021
35321786
An Anatomical Variant That May Save Vision-Widespread Cilioretinal Perfusion in Central Retinal Artery Occlusion.
Dtsch Arztebl Int
2021
34327688
Multiple Evanescent White Dot Syndrome (MEWDS) Associated with Progression of Lacquer Cracks in High Myopia.
Klin Monbl Augenheilkd
2021
33964272
Deep phenotyping of the Cdhr1<sup>-/-</sup> mouse validates its use in pre-clinical studies for human CDHR1-associated retinal degeneration.
Exp Eye Res
2021
34153329
NPHP1 gene-associated nephronophthisis is associated with an occult retinopathy.
Kidney Int
2021
34153144
Prevalence and phenotype associations of complement factor I mutations in geographic atrophy.
Hum Mutat
2021
33465056
Impaired complex I repair causes recessive Leber's hereditary optic neuropathy.
J Clin Invest
2021
32891696
Quantitative Fundus Autofluorescence in ABCA4-Related Retinopathy -Functional Relevance and Genotype-Phenotype Correlation.
Am J Ophthalmol
2021
32580956
Reduced vessel density in deep capillary plexus correlates with retinal layer thickness in choroideremia.
Br J Ophthalmol
2021
33005045
CDHR1-related late-onset macular dystrophy: further insights.
Eye (Lond)
2021
30923132
Retinal findings in carriers of monoallelic <i>ABCC6</i> mutations.
Br J Ophthalmol
2020
31863395
Aflibercept for choroidal neovascularizations secondary to pseudoxanthoma elasticum: a prospective study.
Graefes Arch Clin Exp Ophthalmol
2020
31834130
IMPAIRED DARK ADAPTATION ASSOCIATED WITH A DISEASED BRUCH MEMBRANE IN PSEUDOXANTHOMA ELASTICUM.
Retina
2020
31775146
Transcorneal Electrical Stimulation for the Treatment of Retinitis Pigmentosa: A Multicenter Safety Study of the OkuStim® System (TESOLA-Study).
Ophthalmic Res
2020
31800458
HYPERREFLECTIVE FOCI AS A PATHOGENETIC BIOMARKER IN CHOROIDEREMIA.
Retina
2020
31800456
DARK ADAPTATION IN MACULAR TELANGIECTASIA TYPE 2.
Retina
2020
33090206
Mesopic and Scotopic Light Sensitivity and Its Microstructural Correlates in Pseudoxanthoma Elasticum.
JAMA Ophthalmol
2020
33059378
Laser Pointer: A Possible Risk for the Retina.
Klin Monbl Augenheilkd
2020
33134916
Effect of smoking on macular function and retinal structure in retinitis pigmentosa.
Brain Commun
2020
32646556
Quantitative Fundus Autofluorescence and Genetic Associations in Macular, Cone, and Cone-Rod Dystrophies.
Ophthalmol Retina
2020
32644128
Pentosan Polysulfate Maculopathy-Prescribers Should Be Aware.
JAMA Ophthalmol
2020
32724727
Assessment of AAV Dual Vector Safety in the<i>Abca4</i><sup>-/-</sup> Mouse Model of Stargardt Disease.
Transl Vis Sci Technol
2020
32586743
Macular Telangiectasia Type 2: Visual Acuity, Disease End Stage, and the MacTel Area: MacTel Project Report Number 8.
Ophthalmology
2020
32442430
Late-onset Pseudoxanthoma Elasticum Associated with a Hypomorphic ABCC6 Variant.
Am J Ophthalmol
2020
32147488
Peripapillary Sparing in Autosomal Recessive Bestrophinopathy.
Ophthalmol Retina
2020
32398620
Central Retinal Artery Occlusion Following Prone Transcranial Surgery for Craniosynostosis and Discussion of Risk Factors.
J Craniofac Surg
2020
30466340
Electrophysiological verification of enhanced S-cone syndrome caused by a novel c.755T>C NR2E3 missense variant.
Ophthalmic Genet
2019
1 - 50 of 205
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Marcus Fruttiger
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Andrew R Webster
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Michel Michaelides
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