Tomas Aleman et al. @ScheieEye@ChildrensPhila@cideciya study Retinal Degeneration Associated With Biallelic RDH12 Variants: Longitudinal Evaluation of Retinal Structure and Visual Function in Pediatric Patients, https://t.co/hBSaSAFv8S.
New research out in @TheLancet demonstrates the safety & efficacy of ATSN-101 gene therapy for improving vision in patients with Leber congenital amaurosis caused by GUCY2D mutations ft. @cideciya & Tomas Aleman (@ScheieEye) https://t.co/YQ0aqpxkGW
CHRD co-directors Dr. Cideciyan & Dr. Aleman led a gene therapy trial for LCA1, a rare retinal disease, achieving 100x sight improvement sustained for 1 year. The trial focused on ATSN-101, a subretinal gene therapy. #GeneTherapy#PennMedicine#Ophthalmology#Research#Innovation
Artur V. Cideciyan @cideciya et al. @ScheieEye describe a treatment strategy with gene editing for late-onset retinal degeneration caused by a founder variant in C1QTNF5.
https://t.co/cJTpB64I7b
A first-in-human clinical trial to treat NPHP5 Retinal Degeneration, led by Tomas Aleman, MD, Artur Cideciyan, PhD, Gustavo Aguirre, VMD, PhD & William Beltran, DVM, PhD, was selected for the BGTC Clinical Trial Portfolio, announced at @ASGCTherapy annual meeting. @ScheieEye
Artur Cideciyan @cideciya et al @ScheieEye evaluate rod and cone function and outer retinal structure in macular lesions and surrounding extralesional areas of patients with autosomal dominant Best vitelliform macular dystrophy caused by BEST1 mutations
https://t.co/mXVAbeOxd2
Retina Conference 2021: have you registered yet? Visit https://t.co/oAuVM1ZuI3 and register for free for our Scientific Day, 5th of November. Our wonderful speakers include @edelmurphy2, Bo Chen, Prof @cideciya and more. #Retina21#conference#Retina21
Ocular theranostics at #ARVO2021 today 3:30pm EDT.
I will present gene-based therapies in patients with CEP290-LCA and in dogs with NPHP5-LCA.
Robert Zawadzki, Jennifer Kang-Mieler, Karl Csaky, Ursula Schmidt-Erfurth, Valeria Cant…https://t.co/iY96uqLY7H https://t.co/0vWVGXP7qj
Night vision in the RP macula – slow progress towards platform-independent measurements. Today at #ARVO2021, please visit poster by Arun Kumar Krishnan, post-doctoral fellow in my lab, describing rod function in retinitis pigmentosa obtained with MP-1S an…https://t.co/hWnyACzKGV
A @PennMedicine patient w/ Leber congenital amaurosis- which causes genetic childhood #blindness- demonstrated sustained improvement of vision 15 mos after 1 interocular injection of #sepofarsen ft. @cideciya, Samuel Jacobson & Joan O'Brien (@ScheieEye) https://t.co/ZZvoevzjrb
Post hoc analyses and follow-up of a patient with Leber congenital amaurosis treated with the antisense oligonucleotide sepofarsen indicate sustained improvement of vision 15 months after receiving a single dose of the drug. @cideciya#ASO https://t.co/t9wGTwcf2q