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Michalis Georgiou

Showing results (11-20 of 96) with videos related to

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Ophthalmic Genetics|December 27, 2021
Photoaversion in inherited retinal diseases: clinical phenotypes, biological basis, and qualitative and quantitative assessmentSerena Zaman, Thomas Kane, Mohamed Katta, et al.
International Ophthalmology Clinics|September 29, 2021
Gene Therapy in X-linked Retinitis Pigmentosa Due to Defects in RPGRMichalis Georgiou, Shaima Awadh Hashem, Malena Daich Varela, et al.
Clinical Kidney Journal|March 29, 2021
Joubert syndrome diagnosed renally lateElizabeth Collard, Catherine Byrne, Michalis Georgiou, et al.
BMJ Open Ophthalmology|July 26, 2023
Multimorbidity due to novel pathogenic variants in the <i>WFS1/RP1/NOD2</i> genes: autosomal dominant congenital lamellar cataract, retinitis pigmentosa and Crohn's disease in a British familyVanita Berry, Alexander Ionides, Michalis Georgiou, et al.
International Journal of Retina and Vitreous|July 25, 2022
Outcomes of pars plana vitrectomy following ocular trauma at varying surgical time pointsMuhammad Z Chauhan, Michalis Georgiou, Hytham Al-Hindi, et al.
The British Journal of Ophthalmology|March 29, 2020
Inherited cataracts: molecular genetics, clinical features, disease mechanisms and novel therapeutic approachesVanita Berry, Michalis Georgiou, Kaoru Fujinami, et al.
The British Journal of Ophthalmology|March 20, 2021
Treatments for dry age-related macular degeneration: therapeutic avenues, clinical trials and future directionsThales Antonio Cabral de Guimaraes, Malena Daich Varela, Michalis Georgiou, et al.
Ophthalmic Genetics|May 23, 2020
<i>KCNV2</i> retinopathy: clinical features, molecular genetics and directions for future therapyThales A C De Guimaraes, Michalis Georgiou, Anthony G Robson, et al.
The British Journal of Ophthalmology|March 13, 2021
Leber congenital amaurosis/early-onset severe retinal dystrophy: current management and clinical trialsMalena Daich Varela, Thales Antonio Cabral de Guimaraes, Michalis Georgiou, et al.
The British Journal of Ophthalmology|January 26, 2019
Progressive cone and cone-rod dystrophies: clinical features, molecular genetics and prospects for therapyJasdeep S Gill, Michalis Georgiou, Angelos Kalitzeos, et al.
Pageof 10

Showing results (11-20 of 96) with videos related to

Sort By:
Pageof 10
Ophthalmic Genetics|December 27, 2021
Photoaversion in inherited retinal diseases: clinical phenotypes, biological basis, and qualitative and quantitative assessmentSerena Zaman, Thomas Kane, Mohamed Katta, et al.
International Ophthalmology Clinics|September 29, 2021
Gene Therapy in X-linked Retinitis Pigmentosa Due to Defects in RPGRMichalis Georgiou, Shaima Awadh Hashem, Malena Daich Varela, et al.
Clinical Kidney Journal|March 29, 2021
Joubert syndrome diagnosed renally lateElizabeth Collard, Catherine Byrne, Michalis Georgiou, et al.
BMJ Open Ophthalmology|July 26, 2023
Multimorbidity due to novel pathogenic variants in the <i>WFS1/RP1/NOD2</i> genes: autosomal dominant congenital lamellar cataract, retinitis pigmentosa and Crohn's disease in a British familyVanita Berry, Alexander Ionides, Michalis Georgiou, et al.
International Journal of Retina and Vitreous|July 25, 2022
Outcomes of pars plana vitrectomy following ocular trauma at varying surgical time pointsMuhammad Z Chauhan, Michalis Georgiou, Hytham Al-Hindi, et al.
The British Journal of Ophthalmology|March 29, 2020
Inherited cataracts: molecular genetics, clinical features, disease mechanisms and novel therapeutic approachesVanita Berry, Michalis Georgiou, Kaoru Fujinami, et al.
The British Journal of Ophthalmology|March 20, 2021
Treatments for dry age-related macular degeneration: therapeutic avenues, clinical trials and future directionsThales Antonio Cabral de Guimaraes, Malena Daich Varela, Michalis Georgiou, et al.
Ophthalmic Genetics|May 23, 2020
<i>KCNV2</i> retinopathy: clinical features, molecular genetics and directions for future therapyThales A C De Guimaraes, Michalis Georgiou, Anthony G Robson, et al.
The British Journal of Ophthalmology|March 13, 2021
Leber congenital amaurosis/early-onset severe retinal dystrophy: current management and clinical trialsMalena Daich Varela, Thales Antonio Cabral de Guimaraes, Michalis Georgiou, et al.
The British Journal of Ophthalmology|January 26, 2019
Progressive cone and cone-rod dystrophies: clinical features, molecular genetics and prospects for therapyJasdeep S Gill, Michalis Georgiou, Angelos Kalitzeos, et al.
Pageof 10