Zobrazeno 1 - 10
of 930
pro vyhledávání: '"FAF, fundus autofluorescence"'
Autor:
Nikolas Pontikos, Kamron N. Khan, Genevieve A. Wright, Michalis Georgiou, Monica Armengol, Giuseppe Casalino, Michel Michaelides, Parampal S. Grewal, Andrew R. Webster, Anthony G. Robson
Publikováno v:
Ophthalmology
Purpose To investigate the clinical course, genetic findings, and phenotypic spectrum of autosomal recessive bestrophinopathy (ARB) in a large cohort of children and adults. Design Retrospective case series. Participants Patients with a detailed clin
Autor:
Camiel J. F. Boon, Emanuel R. de Carvalho, Michel Michaelides, Anthony G. Robson, Andrew A. Webster, Gavin Arno
Publikováno v:
Ophthalmology. Retina
Purpose To describe the detailed phenotype, long-term clinical course, clinical variability, and genotype of patients with enhanced S-cone syndrome (ESCS). Design Retrospective case series. Participants Fifty-six patients with ESCS. Methods Clinical
Autor:
Konstantinou, Eleni K.1,2 (AUTHOR), Shaikh, Noreen1,3 (AUTHOR), Ramsey, David J.1,2 (AUTHOR) David.J.Ramsey@lahey.org
Publikováno v:
Ophthalmic Genetics. Apr2023, Vol. 44 Issue 2, p175-181. 7p.
Autor:
Melanie A. Schmitt, James N. Ver Hoeve, Elizabeth R. Kellom, Tyler Etheridge, Rachel M. Sullivan
Publikováno v:
American Journal of Ophthalmology Case Reports
American Journal of Ophthalmology Case Reports, Vol 20, Iss, Pp 100873-(2020)
American Journal of Ophthalmology Case Reports, Vol 20, Iss, Pp 100873-(2020)
Purpose We present 3 cases of Alstrom syndrome (ALMS) that highlight the importance of the ophthalmic exam, as well as the diagnostic challenges and management considerations of this ultra-rare disease. Observations The first case is of a 2-year-old
Autor:
Mehat, Manjit S, Sundaram, Venki, Ripamonti, Caterina, Robson, Anthony G, Smith, Alexander J, Borooah, Shyamanga, Robinson, Martha, Rosenthal, Adam N, Innes, William, Weleber, Richard G, Lee, Richard W J, Crossland, Michael, Rubin, Gary S, Dhillon, Baljean, Steel, David H W, Anglade, Eddy, Lanza, Robert P, Ali, Robin R, Michaelides, Michel, Bainbridge, James W B
Publikováno v:
Ophthalmology
Mehat, M S, Sundaram, V, Ripamonti, C, Robson, A G, Smith, A J, Borooah, S, Robinson, M, Rosenthal, A N, Innes, W, Weleber, R G, Lee, R W J, Crossland, M, Rubin, G S, Dhillon, B, Steel, D H W, Anglade, E, Lanza, R P, Ali, R R, Michaelides, M & Bainbridge, J W B 2018, ' Transplantation of Human Embryonic Stem Cell-Derived Retinal Pigment Epithelial Cells in Macular Degeneration ', Ophthalmology: Journal of The American Academy of Ophthalmology . https://doi.org/10.1016/j.ophtha.2018.04.037
Mehat, M S, Sundaram, V, Ripamonti, C, Robson, A G, Smith, A J, Borooah, S, Robinson, M, Rosenthal, A N, Innes, W, Weleber, R G, Lee, R W J, Crossland, M, Rubin, G S, Dhillon, B, Steel, D H W, Anglade, E, Lanza, R P, Ali, R R, Michaelides, M & Bainbridge, J W B 2018, ' Transplantation of Human Embryonic Stem Cell-Derived Retinal Pigment Epithelial Cells in Macular Degeneration ', Ophthalmology: Journal of The American Academy of Ophthalmology . https://doi.org/10.1016/j.ophtha.2018.04.037
PURPOSE: Transplantation of human embryonic stem cell (hESC)-derived retinal pigment epithelial (RPE) cells offers the potential for benefit in macular degeneration. Previous trials have reported improved visual acuity (VA), but lacked detailed analy
Autor:
Leo, Sheck, Wayne I L, Davies, Phillip, Moradi, Anthony G, Robson, Neruban, Kumaran, Alki C, Liasis, Andrew R, Webster, Anthony T, Moore, Michel, Michaelides
Publikováno v:
Ophthalmology
Purpose To investigate and describe in detail the demographics, functional and anatomic characteristics, and clinical course of Leber congenital amaurosis (LCA) associated with mutations in the CEP290 gene (LCA-CEP290) in a large cohort of adults and
Autor:
Kamron N, Khan, Melissa, Kasilian, Omar A R, Mahroo, Preena, Tanna, Angelos, Kalitzeos, Anthony G, Robson, Kazushige, Tsunoda, Takeshi, Iwata, Anthony T, Moore, Kaoru, Fujinami, Michel, Michaelides
Publikováno v:
Ophthalmology
Purpose To describe the earliest features of ABCA4-associated retinopathy. Design Case series. Participants Children with a clinical and molecular diagnosis of ABCA4-associated retinopathy without evidence of macular atrophy. Methods The retinal phen
Autor:
Papasavvas, Ioannis1,2 (AUTHOR) i.s.papasavvas@gmail.com, Tucker, William R.2 (AUTHOR), Mantovani, Alessandro3 (AUTHOR), Fabozzi, Lorenzo2 (AUTHOR), Herbort Jr, Carl P.1 (AUTHOR) cph@herbortuveitis.ch
Publikováno v:
Journal of Ophthalmic Inflammation & Infection. 12/4/2024, Vol. 14 Issue 1, p1-36. 36p.
Autor:
Zhang, Sairi1 (AUTHOR), Rickels, Kaersti L.1 (AUTHOR), Krishnan, Vignesh1 (AUTHOR), Uwaydat, Sami H.2 (AUTHOR) SHUwaydat@uams.edu
Publikováno v:
Journal of Ophthalmic Inflammation & Infection. 10/18/2024, Vol. 14 Issue 1, p1-9. 9p.
Autor:
Karaca, Cagatay1, Ozer, Furkan2, Sevim, Duygu Gulmez1 duygugsevim@gmail.com, Erdoğan, Osman1, Unlu, Metin1
Publikováno v:
Journal of Clinical Practice & Research. Sep2024, Vol. 46 Issue 5, p507-512. 9p.