Michel Michaelides
Overview
Explore the profile of Michel Michaelides including associated specialties, affiliations and a list of published articles.
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401
Citations
8850
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Recent Articles
1.
Laich Y, Georgiou M, Fujinami K, Varela M, Fujinami-Yokokawa Y, Hashem S, et al.
Ophthalmol Retina
. 2025 Mar;
PMID: 40086732
Purpose: To analyze the retinal imaging findings and natural history of Best vitelliform macular dystrophy (BVMD). Design: Single-center retrospective, consecutive, observational study. Participants: Patients with a clinical diagnosis of BVMD,...
2.
Gandhewar R, Guimaraes T, Sen S, Pontikos N, Moghul I, Empeslidis T, et al.
Graefes Arch Clin Exp Ophthalmol
. 2025 Mar;
PMID: 40059223
Macular fibrosis is an end-stage complication of neovascular Age-related Macular Degeneration (nAMD) with a complex and multifactorial pathophysiology that can lead to significant visual impairment. Despite the success of anti-vascular...
3.
Duncan J, Liang W, Maguire M, Audo I, Ayala A, Birch D, et al.
Am J Ophthalmol
. 2025 Mar;
PMID: 40057408
No abstract available.
4.
Michaelides M, Laich Y, Wong S, Oluonye N, Zaman S, Kumaran N, et al.
Lancet
. 2025 Feb;
405(10479):648-657.
PMID: 39986747
Background: Retinal dystrophy caused by genetic deficiency of AIPL1 causes severe and rapidly progressive impairment of sight from birth. We sought to evaluate whether early intervention by gene supplementation therapy...
5.
Allon G, Lin S, Robson A, Arno G, Neveu M, Hysi P, et al.
Invest Ophthalmol Vis Sci
. 2025 Feb;
66(2):50.
PMID: 39969478
Purpose: To report findings in GUCA1A-associated retinopathy, a rare autosomal-dominant retinopathy. Methods: Clinical features and investigations from molecularly confirmed patients at a large referral center were analyzed (retrospective cohort study)....
6.
Branham K, Samarakoon L, Audo I, Ayala A, Cheetham J, Daiger S, et al.
Invest Ophthalmol Vis Sci
. 2025 Feb;
66(2):12.
PMID: 39908130
Purpose: The Foundation Fighting Blindness (FFB) Consortium is a collaboration of 41 international clinical centers that manage patients affected with inherited retinal diseases (IRDs). The annual Consortium gene poll was...
7.
Woof W, de Guimaraes T, Al-Khuzaei S, Varela M, Sen S, Bagga P, et al.
Ophthalmol Sci
. 2025 Feb;
5(2):100652.
PMID: 39896422
Purpose: To quantify relevant fundus autofluorescence (FAF) features cross-sectionally and longitudinally in a large cohort of patients with inherited retinal diseases (IRDs). Design: Retrospective study of imaging data. Participants: Patients...
8.
Gardner J, Jovanovic K, Ottaviani D, Melo U, Jackson J, Guarascio R, et al.
Am J Hum Genet
. 2025 Feb;
112(3):523-536.
PMID: 39892393
In two unrelated families with X-linked inherited retinal dystrophy, identification of the causative variants was elusive. Interrogation of the next-generation sequencing (NGS) data revealed a "dark" intergenic region on Xq27.1...
9.
Vanzara A, Schiff E, Lin S, Pulido J, Michaelides M, Webster A, et al.
Eye (Lond)
. 2025 Jan;
PMID: 39875726
No abstract available.
10.
Quinodoz M, Rodenburg K, Cvackova Z, Kaminska K, de Bruijn S, Iglesias-Romero A, et al.
medRxiv
. 2025 Jan;
PMID: 39830270
The U4 small nuclear RNA (snRNA) forms a duplex with the U6 snRNA and, together with U5 and ~30 proteins, is part of the U4/U6.U5 tri-snRNP complex, located at the...