Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Stanley Lambertus"'
Autor:
Michel M Teussink, Stanley Lambertus, Frits F de Mul, Malgorzata B Rozanowska, Carel B Hoyng, B Jeroen Klevering, Thomas Theelen
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0172635 (2017)
PURPOSE:Current standards and guidelines aimed at preventing retinal phototoxicity during intentional exposures do not specifically evaluate the contribution of endogenous photosensitizers. However, certain retinal diseases are characterized by abnor
Externí odkaz:
https://doaj.org/article/37dcd162444f462fb546e28801f0259f
Autor:
Stanley Lambertus, Nathalie M Bax, Ana Fakin, Joannes M M Groenewoud, B Jeroen Klevering, Anthony T Moore, Michel Michaelides, Andrew R Webster, Gert Jan van der Wilt, Carel B Hoyng
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0174020 (2017)
BACKGROUND:Each inherited retinal disorder is rare, but together, they affect millions of people worldwide. No treatment is currently available for these blinding diseases, but promising new options-including gene therapy-are emerging. Arguably, the
Externí odkaz:
https://doaj.org/article/dad376ea3c914a80810bffc3ef0ac508
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology, 257, 6, pp. 1147-1157
Graefe's Archive for Clinical and Experimental Ophthalmology, 257, 1147-1157
Graefe's Archive for Clinical and Experimental Ophthalmology, 257, 1147-1157
To raise awareness of Stargardt disease (STGD1) patients without fundus abnormalities. Medical records were evaluated for age at onset, initial symptoms and diagnosis, reason for delay of diagnosis, age at STGD1 diagnosis, best-corrected visual acuit
Autor:
Rob J Teunisse, B. Jeroen Klevering, Stanley Lambertus, Nathalie M. Bax, Carel B. Hoyng, Patty P.A. Dhooge, Johannes R.M. Cruysberg, Bart Liefers
Publikováno v:
British Journal of Ophthalmology, 107, 2, pp. 248-253
British Journal of Ophthalmology, 107, 248-253
British Journal of Ophthalmology, 107, 248-253
AimsTo describe the prevalence of the Charles Bonnet syndrome (CBS) and search for potential CBS risk factors in a Dutch Stargardt disease (STGD1) cohort.MethodsEighty-three patients with STGD1 were screened for CBS. They underwent a full eye examina
Autor:
J.M.M. Groenewoud, Patty P.A. Dhooge, Nathalie M. Bax, B. Jeroen Klevering, Esmee H. Runhart, Stanley Lambertus, Carel B. Hoyng
Publikováno v:
Translational Vision Science & Technology, 10, 3
Translational Vision Science & Technology, 10
Translational Vision Science & Technology
Translational Vision Science & Technology, 10
Translational Vision Science & Technology
Purpose The purpose of this study was to evaluate the functional relevance of longitudinal changes in hyperautofluorescent areas and flecks in Stargardt disease (STGD1) using short-wavelength autofluorescence (SW-AF) imaging. Methods In this prospect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2d8a23cbe378a9bb2c9b0939814c42c
https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/232889
https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/232889
Autor:
Laurence H M Pierrache, Reinier O. Schlingemann, Jan Willem R. Pott, Clasien J. Oomen, Jan Roelof Polling, Michelle Hendriks, Hester Y. Kroes, Wendy A. G. van Zelst-Stams, Albert Hofman, Frans P.M. Cremers, Mary J. van Schooneveld, Redmer van Leeuwen, Ramon A. C. van Huet, F. Nienke Boonstra, Mies M. van Genderen, Caroline C W Klaver, Carel B. Hoyng, Maarten Kamermans, Camiel J. F. Boon, Magda A. Meester-Smoor, L. Ingeborgh van den Born, Nathalie M. Bax, Stanley Lambertus, Virginie J. M. Verhoeven, Yvonne de Jong-Hesse, Arthur A.B. Bergen, J Schuil, Astrid S. Plomp, Gabriëlle H.S. Buitendijk, B Jeroen Klevering
Publikováno v:
American Journal of Ophthalmology, 182, 81-89. Elsevier Inc.
Hendriks, M, Verhoeven, V J M, Buitendijk, G H S, Polling, J R, Meester-Smoor, M A, Hofman, A, Kamermans, M, Ingeborgh van den Born, L, Klaver, C C W & RD5000 Consortium 2017, ' Development of Refractive Errors—What Can We Learn From Inherited Retinal Dystrophies? ', American Journal of Ophthalmology, vol. 182, pp. 81-89 . https://doi.org/10.1016/j.ajo.2017.07.008
American Journal of Ophthalmology, 182, 81-89
American Journal of Ophthalmology, 182, 81-89. Elsevier USA
American Journal of Ophthalmology, 182, pp. 81-89
American Journal of Ophthalmology, 182, 81. Elsevier USA
American Journal of Ophthalmology
American journal of ophthalmology, 182, 81-89. Elsevier USA
Hendriks, M, Verhoeven, V J M, Buitendijk, G H S, Polling, J R, Meester-Smoor, M A, Hofman, A, Kamermans, M, Ingeborgh van den Born, L, Klaver, C C W & RD5000 Consortium 2017, ' Development of Refractive Errors—What Can We Learn From Inherited Retinal Dystrophies? ', American Journal of Ophthalmology, vol. 182, pp. 81-89 . https://doi.org/10.1016/j.ajo.2017.07.008
American Journal of Ophthalmology, 182, 81-89
American Journal of Ophthalmology, 182, 81-89. Elsevier USA
American Journal of Ophthalmology, 182, pp. 81-89
American Journal of Ophthalmology, 182, 81. Elsevier USA
American Journal of Ophthalmology
American journal of ophthalmology, 182, 81-89. Elsevier USA
PURPOSE: It is unknown which retinal cells are involved in the retina-to-sclera signaling cascade causing myopia. As inherited retinal dystrophies (IRD) are characterized by dysfunction of a single retinal cell type and have a high risk of refractive
Autor:
Dyon Valkenburg, Boon Cjf., Stanley Lambertus, Carel B. Hoyng, B. J. Klevering, Moritz Lindner, Nathalie M. Bax, Monika Fleckenstein, Frank G. Holz, Cremers Fpm
Publikováno v:
Investigative Ophthalmology & Visual Science, 60(10), 3456-3467
Investigative Ophthalmology and Visual Science, 60, 3456-3467
Investigative ophthalmology & visual science, 60(10), 3456-3467. Association for Research in Vision and Ophthalmology Inc.
Investigative Ophthalmology and Visual Science, 60, 10, pp. 3456-3467
Investigative Ophthalmology and Visual Science, 60, 3456-3467
Investigative ophthalmology & visual science, 60(10), 3456-3467. Association for Research in Vision and Ophthalmology Inc.
Investigative Ophthalmology and Visual Science, 60, 10, pp. 3456-3467
Purpose: To describe foveal sparing (FS) in central retinal dystrophies (RD). Methods: Participants for this retrospective study were identified from the retinal dystrophy database of the Department of Ophthalmology at Radboud University Medical Cent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::828a15fc8dae4d031a91266a0dcdfdf7
http://hdl.handle.net/1887/121069
http://hdl.handle.net/1887/121069
Autor:
Nathalie M. Bax, Esmee H. Runhart, Stanley Lambertus, Frans P.M. Cremers, Dyon Valkenburg, Bart Liefers, Carel B. Hoyng, Clara I. Sánchez
Publikováno v:
Ophthalmology, 126, 1712-1721
Ophthalmology, 126, 12, pp. 1712-1721
Ophthalmology, 126, 12, pp. 1712-1721
Purpose To investigate intersibling phenotypic concordance in Stargardt disease (STGD1). Design Retrospective cohort study. Participants Siblings with genetically confirmed STGD1 and at least 1 available fundus autofluorescence (FAF) image of both ey
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd5e26a6172b8dd7fb388d5ef2791dfd
https://doi.org/10.1016/j.ophtha.2019.07.010
https://doi.org/10.1016/j.ophtha.2019.07.010
Autor:
B. Jeroen Klevering, Lies H. Hoefsloot, Camiel J. F. Boon, Frans P.M. Cremers, Nathalie M. Bax, Stanley Lambertus, Ramon A. C. van Huet, Carel B. Hoyng
Publikováno v:
Ophthalmology: Journal of The American Academy of Ophthalmology
Objective To describe the phenotype and genotype of patients with early-onset Stargardt disease. Design Retrospective cohort study. Participants Fifty-one Stargardt patients with age at onset ≤10 years. Methods We reviewed patient medical records f
Publikováno v:
Macular Dystrophies ISBN: 9783319266190
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61b0eebebc1f6159ed0dc31661f38483
https://doi.org/10.1007/978-3-319-26621-3_3
https://doi.org/10.1007/978-3-319-26621-3_3