Brian Ballios's guest appearances

Brian Ballios

The Retina Channel Podcast

BroadEye: An Ophthalmology Podcast

OwlTail

Dr. Ballios discusses his group's findings on novel mutations in the RCBTB1 gene that can cuase late-onset non-syndromic retinal dystrophies mimicking macular degeneration. Full article: Catomeris AJ, Ballios BG, Sangermano R, Wagner NE, Comander JI, Pierce EA, Place EM, Bujakowska KM, Huckfeldt RM. Novel RCBTB1 variants causing later-onset non-syndromic retinal dystrophy with macular chorioretinal atrophy. Ophthalmic Genet. 2022 Jan 20:1-8. doi: 10.1080/13816810.2021.2023196. Epub ahead of print. PMID: 35057699.

Dr. Ballios discusses his group's findings on novel mutations in the RCBTB1 gene that can cuase late-onset non-syndromic retinal dystrophies mimicking macular degeneration. Full article: Catomeris AJ, Ballios BG, Sangermano R, Wagner NE, Comander JI, Pierce EA, Place EM, Bujakowska KM, Huckfeldt RM. Novel RCBTB1 variants causing later-onset non-syndromic retinal dystrophy with macular chorioretinal atrophy. Ophthalmic Genet. 2022 Jan 20:1-8. doi: 10.1080/13816810.2021.2023196. Epub ahead of print. PMID: 35057699.

E59-Novel RCBTB1 variants and late-onset retinal dystrophy- Dr. Brian Ballios

Ophthalmologist and vision science researcher Dr. Brian Ballios provides an overview of stem cell therapies for inherited retinal diseases, including Retinitis Pigmentosa. Dr. Ballios further discusses the importance of genetic testing, highlighting that knowledge of a patient's underlying mutation is often required to access clinical trials and approved therapies. 

Ophthalmologist and vision science researcher Dr. Brian Ballios provides an overview of stem cell therapies for inherited retinal diseases, including Retinitis Pigmentosa. Dr. Ballios further discusses the importance of genetic testing, highlighting that knowledge of a patient's underlying mutation is often required to access clinical trials and approved therapies.