Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Adam M. Hanif"'
Autor:
Adam M. Hanif, Benjamin K. Young
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 36, Iss , Pp 102113- (2024)
Externí odkaz:
https://doaj.org/article/9458d74911234bbeb6ef653fb027dc7a
Autor:
Jieming Fu, Moe H. Aung, Megan C. Prunty, Adam M. Hanif, Lauren M. Hutson, Jeffrey H. Boatright, Machelle T. Pardue
Publikováno v:
Pharmaceutics, Vol 13, Iss 8, p 1154 (2021)
Purpose: Previous studies demonstrated that systemic treatment with tauroursodeoxycholic acid (TUDCA) is protective in in vivo mouse models of retinal degeneration and in culture models of hyperglycemia. This study tested the hypothesis that TUDCA wi
Externí odkaz:
https://doaj.org/article/d222b24439ae45188e9941f27910997b
Autor:
Benjamin I. Meyer, G. Baker Hubbard, Phoebe D. Lenhart, Adam M. Hanif, Nieraj Jain, Parker J. Williams
Publikováno v:
RETINAL Cases & Brief Reports. 16:762-765
PURPOSE Adams-Oliver syndrome is a rare, inherited disorder of embryologic development that affects multiple systems. Ocular manifestations have been poorly characterized due to the low prevalence and high mortality of the disease when it is associat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65c6b444002dd131142c0a55b14f1396
https://doi.org/10.1097/icb.0000000000001073
https://doi.org/10.1097/icb.0000000000001073
Publikováno v:
Survey of Ophthalmology. 67:83-96
Pentosan polysulfate sodium (PPS), a semisynthetic sulfated polysaccharide, is the only FDA-approved oral therapy for interstitial cystitis. Recent studies have described a progressive, vision-threatening macular condition associated with long-term P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a12ed85bfab1fe5df48804695d9e1cc
https://doi.org/10.1016/j.survophthal.2021.05.005
https://doi.org/10.1016/j.survophthal.2021.05.005
Publikováno v:
Ophthalmology Retina. 4:1196-1201
Purpose To evaluate whether pentosan polysulfate (PPS) maculopathy manifests distinctive characteristics that permit differentiation from hereditary maculopathies with multimodal fundus imaging. Design Retrospective review. Participants Emory Eye Cen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0fb85c1f606961f1b3a9d44b7890269
https://doi.org/10.1016/j.oret.2020.05.008
https://doi.org/10.1016/j.oret.2020.05.008
Publikováno v:
International Ophthalmology Clinics. 59:173-194
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36408051b11658fdddaaac0f9b7cf59c
https://doi.org/10.1097/iio.0000000000000262
https://doi.org/10.1097/iio.0000000000000262
Publikováno v:
Ophthalmology. Retina. 4(12)
To evaluate whether pentosan polysulfate (PPS) maculopathy manifests distinctive characteristics that permit differentiation from hereditary maculopathies with multimodal fundus imaging.Retrospective review.Emory Eye Center databases were queried for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c09d5972b2257028ec07e50fdc2049ab
https://pubmed.ncbi.nlm.nih.gov/32446908
https://pubmed.ncbi.nlm.nih.gov/32446908
Publikováno v:
Ocular Immunology and Inflammation. 27:706-708
Autosomal dominant neovascular inflammatory vitreoretinopathy (ADNIV) is a rare autoimmune condition that typically presents as progressive uveitis and vitreoretinal degeneration between the second and third decades of life. Though traditionally attr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34e838ae43d0df3d330ce62d96006720
https://doi.org/10.1080/09273948.2019.1582783
https://doi.org/10.1080/09273948.2019.1582783
Publikováno v:
Journal of American Association for Pediatric Ophthalmology and Strabismus. 25:e60
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f66b91a7f18378390a33cc1af889a513
https://doi.org/10.1016/j.jaapos.2021.08.227
https://doi.org/10.1016/j.jaapos.2021.08.227
Autor:
Nieraj Jain, Adam M. Hanif
Publikováno v:
Ophthalmic Surgery, Lasers and Imaging Retina. 50
A patient with a family history of molecularly confirmed Sorsby fundus dystrophy (SFD) presented with 9 years of progressive, bilateral central vision loss. Specific mutation analysis of the TIMP3 gene confirmed SFD, identifying a pathogenic mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e055b5f57b1701423bc624bbacc8672
https://doi.org/10.3928/23258160-20190806-15
https://doi.org/10.3928/23258160-20190806-15