Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Allan E. Kreiger"'
Autor:
Andrew Clark, Erik A. Souverein, Daniel B. Rootman, Dong Yang, Allan E. Kreiger, Aaron Nagiel
Publikováno v:
RETINAL Cases & Brief Reports.
Autor:
Clémence, Bonnet, Ismael, Chehaibou, Colin A, McCannel, Tara A, McCannel, Pradeep S, Prasad, Allan E, Kreiger, Steven D, Schwartz, Anthony, Aldave, Jean-Pierre, Hubschman
Publikováno v:
Retina. 42:957-966
To evaluate the mid-term outcomes of pars plana vitrectomy performed for retinal detachment (RD) repair after Boston Type 1 keratoprosthesis (KPro) implantation.Retrospective review of medical records of KPro implanted at the Stein Eye Institute pres
Autor:
Clémence Bonnet, Ismael Chehaibou, Colin A. McCannel, Tara A. McCannel, Pradeep S. Prasad, Allan E. Kreiger, Steven D. Schwartz, Anthony Aldave, Jean-Pierre Hubschman
Publikováno v:
Retina. 43:e31-e32
Autor:
Jean-Pierre Hubschman, Ismael Chehaibou, Mercedes Rodriguez, Cameron Pole, Gilad Rabina, Steven D. Schwartz, Moritz Pettenkofer, Allan E. Kreiger
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology. 260:1509-1516
To determine the characteristics and appearance rate of epiretinal proliferation (ERP) on SD-OCT after surgery for rhegmatogenous retinal detachment (RRD) repair. One hundred eight eyes of 108 patients who underwent one or more surgeries for RRD were
Autor:
Kook Lee, Allan E. Kreiger, Elisha C Garg, David Sarraf, K. Bailey Freund, Suzanne Yzer, Yoichi Sakurada, Srinivas R. Sadda, Sandra Liakopoulos, Scott Eugene Pautler, Nopasak Phasukkijwatana, Atchara Amphornphruet, David Xu, Won Ki Lee
Publikováno v:
British Journal of Ophthalmology, 106, 576-581
British Journal of Ophthalmology, 106, 4, pp. 576-581
British Journal of Ophthalmology, 106, 4, pp. 576-581
Background/AimsTo analyse the long-term anatomic and visual outcomes of patients with peripapillary pachychoroid syndrome (PPS), a recently described entity in the pachychoroid disease spectrum.MethodsThis study retrospectively included patients from
Autor:
Moritz, Pettenkofer, Ismael, Chehaibou, Cameron, Pole, Mercedes, Rodriguez, Gilad, Rabina, Allan E, Kreiger, Steven D, Schwartz, Jean-Pierre, Hubschman
Publikováno v:
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie. 260(5)
To determine the characteristics and appearance rate of epiretinal proliferation (ERP) on SD-OCT after surgery for rhegmatogenous retinal detachment (RRD) repair.One hundred eight eyes of 108 patients who underwent one or more surgeries for RRD were
Autor:
Moritz Pettenkofer, Ismael Chehaibou, Cameron Pole, Mercedes Rodriguez, Gilad Rabina, Allan E. Kreiger, Steven D. Schwartz, Jean‑Pierre Hubschman
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology. 260:1429-1429
Autor:
K. Bailey Freund, Sandeep Randhawa, Won Ki Lee, Allan E. Kreiger, Qingyun Liu, Alex P. Hunyor, Jay M. Stewart, David Sarraf, Mansour Rahimi, Rosa Dolz-Marco, Catherine A Egan, Lee M. Jampol, Pearse A. Keane, Mayss Al-Sheikh, Nopasak Phasukkijwatana, Aaron Nagiel, Robert A. Lalane
Publikováno v:
Retina. 38:1652-1667
To describe the features of peripapillary pachychoroid syndrome (PPS), a novel pachychoroid disease spectrum (PDS) entity.Medical records of 31 eyes (16 patients) with choroidal thickening associated with intraretinal and/or subretinal fluid in the n
Autor:
Steven D. Schwartz, John D. Pitcher, Jean-Pierre Hubschman, Ehsan Rahimy, Allan E. Kreiger, Christopher J. Gee
Publikováno v:
Retina. 35:303-309
PURPOSE: To investigate anatomical and functional outcomes of vitreoretinal fellow-performed vitrectomy for tractional retinal detachment secondary to proliferative diabetic retinopathy in a county hospital system. METHODS: Consecutive retrospective
Publikováno v:
Retinal casesbrief reports. 12
Purpose The aim of this study was to investigate the presenting sign of retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations, a rare autosomal dominant condition caused by mutations in the TREX1 gene, and to explore the