Publications by authors named "E Averbukh"

Article Synopsis
  • - Gene augmentation therapy shows promise for treating incurable inherited retinal diseases, with intravitreal delivery being explored as a safer method compared to subretinal injections, using Adeno-Associated Viruses (AAV) as delivery vectors.
  • - A study on sheep with CNGA3 achromatopsia assessed the impact of pre-existing neutralizing antibodies (NABs) against AAV on the safety and effectiveness of AAV2.7m8 injections, finding that 21.4% of sheep had pre-operative NABs, mostly affected by age.
  • - Results indicated that while pre-existing NABs did not affect post-operative NAB levels, they significantly heightened the risk of inflammation in the eyes, suggesting important considerations for managing
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Purpose: To evaluate the divergence between the neodymium-doped yttrium aluminum garnet (Nd:YAG) surgical laser and the aiming diode laser beams foci.

Design: Optical analysis and measurements were performed using a Volk Goldmann 3-mirror lens with a Nidek YC-1800 Nd:YAG laser apparatus.

Subjects: None.

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This report describes a case of central serous chorioretinopathy (CSCR) occurring following cessation of terbinafine treatment. A 51-year-old man presented for a routine ophthalmic examination. He was treated with oral terbinafine for onychomycosis up to 3 months before the presentation.

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Sheep carrying a mutated CNGA3 gene exhibit diminished cone function and provide a naturally occurring large animal model of achromatopsia. Subretinal injection of a vector carrying the CNGA3 transgene resulted in long-term recovery of cone function and photopic vision in these sheep. Research is underway to develop efficacious vectors that would enable safer transgene delivery, while avoiding potential drawbacks of subretinal injections.

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The ability of the adult human brain to develop function following correction of congenital deafferentation is controversial. Specifically, cases of recovery from congenital visual deficits are rare. -achromatopsia is a congenital hereditary disease caused by cone-photoreceptor dysfunction, leading to impaired acuity, photoaversion, and complete color blindness.

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