Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Preena Tanna"'
Autor:
Angelos Kalitzeos, Michel Michaelides, Thomas Kane, Navjit Singh, Preena Tanna, Rupert W. Strauss, Kaoru Fujinami, Zaina Bouzia, Michalis Georgiou
Publikováno v:
American Journal of Ophthalmology
Purpose To determine the reliability and repeatability of quantitative evaluation of areas of decreased autofluorescence (DAF) from fundus autofluorescence (FAF) images and track disease progression in children with Stargardt disease (STGD1), and to
Autor:
Michel Michaelides, Preena Tanna, Kaoru Fujinami, Naser Ali, Michalis Georgiou, Neruban Kumaran, Angelos Kalitzeos, Rupert W. Strauss
Publikováno v:
Translational Vision Science & Technology
Purpose To evaluate the reliability of ellipsoid zone (EZ) loss width and area measurements from spectral-domain optical coherence tomography (SD-OCT) images and track disease progression in childhood-onset Stargardt disease (STGD1). Methods Children
Publikováno v:
The British Journal of Ophthalmology
Stargardt disease (STGD1; MIM 248200) is the most prevalent inherited macular dystrophy and is associated with disease-causing sequence variants in the gene ABCA4. Significant advances have been made over the last 10 years in our understanding of bot
Autor:
Michel Michaelides, Jonathan Aboshiha, Neruban Kumaran, Richard G. Weleber, Rupert W. Strauss, Angelos Kalitzeos, Michalis Georgiou, Preena Tanna
Publikováno v:
Translational Vision Science & Technology
Purpose We assess cross-sectional and longitudinal microperimetry and full-field static perimetry-derived retinal sensitivity with conventional and volumetric indices of retinal function in childhood-onset Stargardt disease (STGD1). Methods Subjects
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:
Michel Michaelides, Alexis Visotcky, Melissa Kasilian, Sergey Tarima, James Tee, Joseph Carroll, Rupert W. Strauss, Angelos Kalitzeos, Preena Tanna, Alfredo Dubra
Publikováno v:
Investigative Ophthalmology & Visual Science
PURPOSE: To assess reliability and repeatability of cone density measurements by using confocal and (nonconfocal) split-detector adaptive optics scanning light ophthalmoscopy (AOSLO) imaging. It will be determined whether cone density values are sign
Publikováno v:
British Journal of Ophthalmology; Jan2017, Vol. 102 Issue 1, p25-30, 6p, 1 Color Photograph, 1 Diagram
Autor:
Hyeong-Gon Yu
This book presents the latest knowledge and expert guidance on all aspects of inherited retinal diseases, including molecular genetics, diagnosis, clinical features, general principles of treatment, novel treatment methods, and genetic counseling. Re
Autor:
Gyan Prakash, Takeshi Iwata
This second volume continues with a focus on the state of the art in genetic eye research in Asia and the Pacific. Though there has been an explosion of information on genetic eye research in western countries, more than sixty percent of the human ge