Michalis Georgiou, MD, PhD
@GeoMichalis
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Inherited Retinal Diseases and more | Aspiring Retina Specialist @dukeeyecenter | PhD @moorfields | https://t.co/10ZO18dbOF
Little Rock, AR
Joined March 2013
After 6 years of med school and 4 years of ophthalmology research, intern year, a PhD, 40+ papers, 400+ citations, 3 countries and 2 continents, it’s real. Let me examine your eyes 👀 . #ophthalmology #residency #medtwitter
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RT @NEIDirector: Next-generation phenotyping of inherited retinal diseases: Eye2Gene (AI-driven algorithm). Better-than-expert accuracy for….
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Excited to see advancements in retinal research for X-linked retinitis pigmentosa. The community urges Johnson & Johnson to seek approval for its XLRP gene therapy, offering hope to patients. @MichelMichaelid @UCL_Retina.
fightingblindness.org
Patients have reported life-changing vision improvements after treatment in the Phase 3 LUMEOS trial.
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RT @UKEyeGenetics: Happy #RareDiseaseDay2025! 👁️🧬. Let's make this another unbelievable year of discovery for rare eye diseases!. @MariyaMo….
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🗞️🚨I am incredibly grateful and humbled to be a part of this remarkable team @MichelMichaelid @UCL_Retina that delivered such a meaningful project. It has truly been life-changing and has had a positive impact on the children and their families.
lnkd.in
This link will take you to a page that’s not on LinkedIn
Gene therapy in children with AIPL1-associated severe retinal dystrophy: an open-label, first-in-human interventional study
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Pleasure to see our PDE6A study feature at @AAOjournal @MichelMichaelid.
In patients with PDE6A-retinitis pigmentosa, despite the presence of cystoid macular edema, there was relative stability in macular parameters. @GeoMichalis @MichelMichaelid .
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New Publication @ARVOiovs 👁️. We expand on our previous work on CNGA3-Achromatopsia, longitudinally assessing the foveal cone mosaic preservation with adaptive optics. Kudos to Mohamed and the whole team! @UCL_Retina @AOIPLab @MichelMichaelid .
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RT @dukeeyecenter: It is an honor to host Joseph Carroll, PhD, .Richard O. Shultz, MD & Ruth Works Professor in Ophthalmology from @Medic….
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New in Ophthalmology Retina, our comprehensive analysis of PDE6A-retinopathy. @MichelMichaelid leading and an amazing team of co-authors. This study details the natural history of PDE6A-retinopathy in one of the largest cohort to date.
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New @AJOphthalmology 🚨🧬👁️.Peer review data of one of the most promising trials in IRDs. Proud to be among an amazing group of collaborators! @MichelMichaelid @UCLeye @Moorfields .Safe and well-tolerated, and showed improvements in efficacy assessments.
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Case report 🦄. Diagnosed RP in a patient with albinism, now confirmed for PDE6A-RP and TYR-albinism. Age-matched controls included. Out at AJO Case Reports. #RetinitisPigmentosa #Albinism #Genetics 👁️@MichelMichaelid . Link:.
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Ophthalmology Advocacy Day: Team Arkansas advocating for access to quality eye care, safety, research funding, and a sustainable profession. 👁️. @eyeadvocacy @aao_ophth #myf2024 #Advocacy #EyeCare #ResearchFunding #Arkansas
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New Publication Alert! . Retinal structure in CSNB is stationary and no specific genotype - structure correlates were identified. VA appears to be relatively stable, with rare instances of progression. @MichelMichaelid @tacguimaraes .
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Great pleasure to see our comprehensive review out! @MichelMichaelid.
PRER article from @MichelMichaelid and collaborators who provide expert insight into genetics and imaging of photoreceptor degeneration #RetinaAwarenessMonth #retina #RP @MoorfieldsBRC.@UCLeye @Wills_Eye features https://www.sciencedirect.com/science/article/pii/S1350946224000090
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RT @Alanretina: PRER article from @MichelMichaelid and collaborators who provide expert insight into genetics and imaging of photoreceptor….
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We report the genetic findings, clinical spectrum and natural history of Best vitelliform macular dystrophy (BVMD) in a cohort of 222 children and adults. @MichelMichaelid @Moorfields @UCL_Retina Kudos to Yannik Laich and an amazing group of co-authors!.
Best vitelliform macular dystrophy is a slowly progressive disease and phenotype- genotype correlations can be used for more accurate prognostication and counseling in this phenotypically diverse disorder.
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Fresh off the press @AJOphthalmology our comprehensive analysis of PDE6B-retinopathy. @MichelMichaelid , Shaima Hashem and an amazing team of co-authors. This study details the natural history of PDE6B-retinopathy in one of the largest cohort to date.
ajo.com
To analyze the clinical characteristics, natural history, and genetics of PDE6B-associated retinal dystrophy.
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Fresh off the press at @AJOphthalmology our comperative analysis study for cataract surgical outcomes in eye with retinitis pigmentosa. @ShakarchiAhmed @MichelMichaelid . *Early Surgery .*Safe Surgery.*Good Outcomes.*More CME and PCO.
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New in "Progress in Retina and Eye Research" - a comprehensive review on the incredible work of our IRD community over the past two decades. A milestone mid-career review for @MichelMichaelid (>350 publications) and an early career highlight for me (>70)
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New publication @AAOjournal We analyse @MichelMichaelid @UCL_Retina @Moorfields @UCLeye, the genetic findings, clinical spectrum and natural history of Best vitelliform macular dystrophy (BVMD) in a cohort of 222 children and adults. Report 1:
aaojournal.org
To analyze the genetic findings, clinical spectrum, and natural history of Best vitelliform macular dystrophy (BVMD) in a cohort of 222 children and adults.
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I am thrilled that I will join the Medical Retina Fellowship at Duke Eye Center @dukeeyecenter July 2024! The interview trail was incredible, connecting with so many brilliant individuals. I am deeply grateful to my family, friends, and mentors, especially @MichelMichaelid !
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