Auswahl der wissenschaftlichen Literatur zum Thema „Geographic atrophy“
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Zeitschriftenartikel zum Thema "Geographic atrophy"
STAURENGHI, G. „Geographic atrophy“. Acta Ophthalmologica 90 (06.08.2012): 0. http://dx.doi.org/10.1111/j.1755-3768.2012.4212.x.
Der volle Inhalt der QuelleHolz, Frank G., Erich C. Strauss, Steffen Schmitz-Valckenberg und Menno van Lookeren Campagne. „Geographic Atrophy“. Ophthalmology 121, Nr. 5 (Mai 2014): 1079–91. http://dx.doi.org/10.1016/j.ophtha.2013.11.023.
Der volle Inhalt der QuelleSheikh, Ahmed Bilal, Andrew Lee, Adnan Mallick und Ronni M. Lieberman. „Geographic Atrophy“. Advances in Ophthalmology and Optometry 3, Nr. 1 (August 2018): 205–15. http://dx.doi.org/10.1016/j.yaoo.2018.04.011.
Der volle Inhalt der QuelleSchmitz-Valckenberg, Steffen, Srinivas Sadda, Giovanni Staurenghi, Emily Y. Chew, Monika Fleckenstein und Frank G. Holz. „GEOGRAPHIC ATROPHY“. Retina 36, Nr. 12 (Dezember 2016): 2250–64. http://dx.doi.org/10.1097/iae.0000000000001258.
Der volle Inhalt der QuelleBird, Alan C., Rachel L. Phillips und Gregory S. Hageman. „Geographic Atrophy“. JAMA Ophthalmology 132, Nr. 3 (01.03.2014): 338. http://dx.doi.org/10.1001/jamaophthalmol.2013.5799.
Der volle Inhalt der QuelleTakahashi, Ayako, Sotaro Ooto, Kenji Yamashiro, Hiroshi Tamura, Akio Oishi, Manabu Miyata, Masayuki Hata, Munemitsu Yoshikawa, Nagahisa Yoshimura und Akitaka Tsujikawa. „Pachychoroid Geographic Atrophy“. Ophthalmology Retina 2, Nr. 4 (April 2018): 295–305. http://dx.doi.org/10.1016/j.oret.2017.08.016.
Der volle Inhalt der QuelleGuymer, Robyn H. „Geographic Atrophy Trials“. Ophthalmology Retina 2, Nr. 6 (Juni 2018): 515–17. http://dx.doi.org/10.1016/j.oret.2018.03.004.
Der volle Inhalt der QuelleErgun, Erdem, Michael Stur und Wolfgang Drexler. „Geographic Atrophy Margins“. Ophthalmology 117, Nr. 5 (Mai 2010): 1051. http://dx.doi.org/10.1016/j.ophtha.2010.01.013.
Der volle Inhalt der QuelleNeroev, Vladimir V., Marina V. Zueva, Natalia V. Neroeva, Ludmila A. Katargina, Oksana A. Losanova, Marina V. Ryabina und Irina V. Tsapenko. „Clinical and Functional Characteristics of Secondary Geographic Atrophy Against the Background of Exudative Age-Related Macular Degeneration“. Annals of the Russian academy of medical sciences 76, Nr. 4 (22.10.2021): 384–93. http://dx.doi.org/10.15690/vramn1557.
Der volle Inhalt der QuelleSadda, SriniVas R., und David Sarraf. „Therapeutic Margin for Geographic Atrophy“. JAMA Ophthalmology 139, Nr. 7 (01.07.2021): 751. http://dx.doi.org/10.1001/jamaophthalmol.2021.1414.
Der volle Inhalt der QuelleDissertationen zum Thema "Geographic atrophy"
Takahashi, Ayako. „Photoreceptor Damage and Reduction of Retinal Sensitivity Surrounding Geographic Atrophy in Age-Related Macular Degeneration“. Kyoto University, 2018. http://hdl.handle.net/2433/232112.
Der volle Inhalt der QuelleBiarnés, Pérez Marc 1973. „Increased fundus autofluorescence, a biomarker of lipofuscin content, as a risk factor for the progression of geographic atrophy secondary to age-related macular degeneration“. Doctoral thesis, Universitat Pompeu Fabra, 2014. http://hdl.handle.net/10803/318157.
Der volle Inhalt der QuelleGeographic atrophy (GA) is the advanced form of dry age-related macular degeneration. It is characterized by large areas of retinal pigment epithelium (RPE) atrophy that grow progressively, with concomitant loss of photoreceptors and choriocapillaris. Currently, there is no treatment for this disorder. Lipofuscin build-up within the RPE, which is identifiable by fundus autofluorescence (FAF) as areas of increased autofluorescence, has been linked to GA progression in some studies. Actually, the distribution of hyperautofluorescence on FAF identified some patterns (“phenotypes”), which have been associated with specific rates of disease growth. We conducted a prospective clinical study to simplify the complex classification of FAF patterns and to determine the role of increased FAF, a biomarker of lipofuscin, in the progression of GA.
Sufian, Elfandi. „CLINICAL AND GENETIC CHARACTERISTICS OF JAPANESE PATIENTS WITH AGE-RELATED MACULAR DEGENERATION AND PSEUDODRUSEN“. Kyoto University, 2018. http://hdl.handle.net/2433/232120.
Der volle Inhalt der QuelleCherepanoff, Svetlana. „Age-related macular degeneration: histopathological and serum autoantibody studies“. University of Sydney, 2008. http://hdl.handle.net/2123/2464.
Der volle Inhalt der QuelleBACKGROUND: The accumulation of abnormal extracellular deposits beneath the retinal pigment epithelium characterises the pathology of early age-related macular degeneration. However, the histopathological threshold at which age-related changes become early AMD is not defined, and the effect of each of the deposits (basal laminar deposit and membranous debris) on disease progression is poorly understood. Evidence suggests that macrophages play a key role in the development of AMD lesions, but the influence of basal laminar deposit (BLamD) and membranous debris on the recruitment and programming of local macrophages has not been explored. Although evidence also suggests that inflammation and innate immunity are involved in AMD, the significance of anti-retinal autoantibodies to disesase pathogenesis is not known. AIMS: (i) To determine the histopathological threshold that distinguishes normal ageing from early AMD; (ii) to determine the influence of BLamD and membranous debris on disease progression; (iii) to examine whether distinct early AMD phenotypes exist based on clinicopathological evidence; (iv) to determine the histopathological context in which Bruch’s membrane macrophages first found; (v) to examine the relationship between Bruch’s membrane macrophages and subclinical neovascularisation; (vi) to determine if the progressive accumulation of BLamD and membranous debris alters the immunophenotype of Bruch’s membrane macrophages and/or resident choroidal macrophages; (vii) to determine if the anti-retinal autoantibody profile differs significantly between normal individuals and those with early AMD, neovascular AMD or geographic atrophy; (viii) to examine whether baseline anti-retinal autoantibodies can predict progression to advanced AMD in individuals with early AMD; and (ix) to examine whether baseline anti-retinal autoantibodies can predict vision loss in individuals with neovascular AMD. METHODS:Clinicopathological studies were performed to correlate progressive accumulation of BLamD and membranous debris to fundus characteristics and visual acuity, as well as to sub-macular Bruch’s membrane macrophage count. Immunohistochemical studies were perfomed to determine whether the presence of BLamD and membranous debris altered the programming of Bruch’s membrane or resident choroidal macrophages. The presence of serum anti-retinal autoantibodies was determined by western blotting, and the association with disease progression examined in early and neovascular AMD. RESULTS: The presence of both basal linear deposit (BLinD) and a continuous layer of BLamD represents threshold early AMD histopathologically, which was seen clinically as a normal fundus in the majority of cases. Membranous debris accumulation appeared to influence the pathway of progression from early AMD to advanced AMD. Bruch’s membrane macrophages were first noted when a continuous layer of BLamD and clinical evidence of early AMD were present, and increased with the amount of membranous debris in eyes with thin BLamD. Eyes with subclinical CNV had high macrophage counts and there was some evidence of altered resident choroidal macrophage programming in the presence of BLamD and membranous debris. Serum anti-retinal autoantibodies were found in a higher proportion of early AMD participants compared with both controls and participants with neovascular AMD, and in a higher proportion of individuals with atrophic AMD compared to those with neovascular AMD. The presence of baseline anti-retinal autoantibodies in participants with early AMD was not associated with progression to advanced AMD. Participants with neovascular AMD lost more vision over 24 months if they had IgG autoantibodies at baseline compared to autoantibody negative participants. CONCLUSIONS: The finding that eyes with threshold early AMD appear clinically normal underscores the need to utilise more sophisticated tests to enable earlier disease detection. Clinicopathological evidence suggests two distinct early AMD phenotypes, which follow two pathways of AMD progression. Macrophage recruitment and programming may be altered by the presence of BLamD and membranous debris, highlighting the need to further characterise the biology of human resident choroidal macropahges. Anti-retinal autoantibodies can be found in both control and AMD sera, and future approaches that allow the examination of subtle changes in complex repertoires will determine whether they are involved in AMD disease pathogenesis.
Cherepanoff, Svetlana. „Age-related macular degeneration: histopathological and serum autoantibody studies“. Thesis, The University of Sydney, 2007. http://hdl.handle.net/2123/2464.
Der volle Inhalt der QuelleTeixeira, Luís Miguel Xavier Alves de Castro. „Role of Choroidal Tickness and Cataract Surgery in the progression of Geographic Atrophy“. Master's thesis, 2014. https://repositorio-aberto.up.pt/handle/10216/72936.
Der volle Inhalt der QuelleTeixeira, Luís Miguel Xavier Alves de Castro. „Role of Choroidal Tickness and Cataract Surgery in the progression of Geographic Atrophy“. Dissertação, 2014. https://repositorio-aberto.up.pt/handle/10216/72936.
Der volle Inhalt der QuelleTavares, Samuel Oliveira Ferreira. „Papel dos anti-VEGF na atrofia macular: consequência do tratamento ou progressão natural da Degenerescência Macular da Idade?“ Master's thesis, 2021. http://hdl.handle.net/10316/98319.
Der volle Inhalt der QuelleDesde a introdução dos anti-VEGF como abordagem terapêutica para a DMI neovascular que estes se têm mantido como único tratamento manifestamente eficaz no combate à progressão da doença. A possibilidade de um maior desenvolvimento de atrofia macular nos olhos dos doentes tratados, porém, tem vindo a ser levantada. Atualmente, é ainda difícil estabelecer com segurança se a atrofia macular verificada neste contexto se deve, efetivamente, aos fármacos anti-VEGF, se, por outro lado, traduz somente a progressão natural da DMI atrófica. Com a elaboração deste trabalho, pretendeu-se avaliar os resultados dos principais estudos publicados sobre a temática e perceber a validade das principais hipóteses explicativas para a associação encontrada. Elaborou-se, para tal, uma pesquisa na base de dados online PubMed, selecionando-se os estudos de maior relevância. Posteriormente, procedeu-se a uma análise comparativa dos mesmos. A obtenção de uma resposta inequívoca não foi conseguida. Perceberam-se as limitações ao confronto dos diferentes estudos e exploraram-se os fatores envolvidos em potenciais conclusões discrepantes. Contudo, tornou-se claro que a evidência mais atual atesta a segurança dos fármacos anti-VEGF. A sua utilização é fortemente encorajada no contexto da DMI neovascular, e os potenciais riscos envolvidos são largamente suplantados pelos seus benefícios.
Since the introduction of anti-VEGF drugs as a therapeutical approach for neovascular AMD that this has remained the only clearly effective treatment to fight the progression of the disease. The possibility of a larger development of macular atrophy in the eyes of treated patients, however, has been raised in recent years. Nowadays, it is still difficult to assess clearly if the identified macular atrophy in this context is due, truly, to anti-VEGF drugs, or, on the other hand, if it merely reflects the natural progression of atrophic AMD. With the elaboration of this paper, it was intended for one to evaluate the results of the leading studies published on the subject, and to apprehend the validity of the main hypothesis that try to explain the verified association. To do that, a research using the online database PubMed was made, being selected the studies with the higher relevance. Subsequently, one proceeded to a comparative analysis of said studies.It was not possible to obtain an unequivocal answer on the proposed topic. The limitations in contrasting the different studies were ascertained, and the various factors involved in potentially discrepant conclusions were explored. Nonetheless, it has been made clear that the most recent scientifical evidence attests the safety of anti-VEGF drugs. Its use is strongly encouraged in the context of neovascular AMD, and any potentially existing risk is largely outweighed by its unmistakable benefits.
Buchteile zum Thema "Geographic atrophy"
Pilotto, Elisabetta, und Francesca Guidolin. „Geographic Atrophy“. In Microperimetry and Multimodal Retinal Imaging, 77–88. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-40300-2_8.
Der volle Inhalt der QuelleLindner, Moritz, Monika Fleckenstein, Steffen Schmitz-Valckenberg und Frank G. Holz. „Atrophy, Geographic“. In Encyclopedia of Ophthalmology, 1–3. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-35951-4_1125-1.
Der volle Inhalt der QuelleLindner, Moritz, Monika Fleckenstein, Steffen Schmitz-Valckenberg und Frank G. Holz. „Atrophy, Geographic“. In Encyclopedia of Ophthalmology, 207–9. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-540-69000-9_1125.
Der volle Inhalt der QuelleFleckenstein, M., S. Schmitz-Valckenberg, J. S. Sunness und F. G. Holz. „Geographic Atrophy“. In Age-related Macular Degeneration, 121–38. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-22107-1_8.
Der volle Inhalt der QuelleLindner, Moritz, Monika Fleckenstein, Julia Steinberg, Steffen Schmitz-Valckenberg und Frank G. Holz. „Geographic Atrophy Secondary to Age-Related Macular Degeneration“. In Spectral Domain Optical Coherence Tomography in Macular Diseases, 169–82. New Delhi: Springer India, 2016. http://dx.doi.org/10.1007/978-81-322-3610-8_14.
Der volle Inhalt der QuelleYang, Qi, Neha Anegondi, Verena Steffen, Simon S. Gao, Julia Cluceru, Christina Rabe, Jian Dai und Daniela Ferrara. „Uncertainty-Aware Geographic Atrophy Progression Prediction from Fundus Autofluorescence“. In Lecture Notes in Computer Science, 29–38. Cham: Springer Nature Switzerland, 2022. http://dx.doi.org/10.1007/978-3-031-17721-7_4.
Der volle Inhalt der QuelleMarmor, M. F. „Age-related geographic atrophy and pattern dystrophy of the RPE“. In Documenta Ophthalmologica Proceedings Series, 291–96. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5137-5_48.
Der volle Inhalt der QuelleBearelly, Srilaxmi, und Scott W. Cousins. „Fundus Autofluorescence Imaging in Age-Related Macular Degeneration and Geographic Atrophy“. In Retinal Degenerative Diseases, 395–402. New York, NY: Springer New York, 2009. http://dx.doi.org/10.1007/978-1-4419-1399-9_45.
Der volle Inhalt der QuelleJoussen, Antonia M., Jan van Meurs und Bernd Kirchhof. „Autologous Translocation of the Choroid and RPE in Patients with Geographic Atrophy“. In Essentials in Ophthalmology, 143–52. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-33670-9_12.
Der volle Inhalt der QuelleLi, Yuchun, Sijie Niu, Zexuan Ji und Qiang Chen. „Automated and Robust Geographic Atrophy Segmentation for Time Series SD-OCT Images“. In Pattern Recognition and Computer Vision, 249–61. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-03398-9_22.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Geographic atrophy"
Lee, Noah, R. Theodore Smith und Andrew F. Laine. „Interactive segmentation for geographic atrophy in retinal fundus images“. In 2008 42nd Asilomar Conference on Signals, Systems and Computers. IEEE, 2008. http://dx.doi.org/10.1109/acssc.2008.5074488.
Der volle Inhalt der QuelleHu, Zhihong, Ziyuan Wang und SriniVas Sadda. „Automated segmentation of geographic atrophy using deep convolutional neural networks“. In Computer-Aided Diagnosis, herausgegeben von Kensaku Mori und Nicholas Petrick. SPIE, 2018. http://dx.doi.org/10.1117/12.2287001.
Der volle Inhalt der QuelleHu, Zhihong, Gerard G. Medioni, Matthias Hernandez und SriniVas R. Sadda. „Supervised pixel classification for segmenting geographic atrophy in fundus autofluorescene images“. In SPIE Medical Imaging, herausgegeben von Stephen Aylward und Lubomir M. Hadjiiski. SPIE, 2014. http://dx.doi.org/10.1117/12.2043178.
Der volle Inhalt der QuelleDevisetti, K., T. P. Karnowski, L. Giancardo, Y. Li und E. Chaum. „Geographic atrophy segmentation in infrared and autofluorescent retina images using supervised learning“. In 2011 33rd Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2011. http://dx.doi.org/10.1109/iembs.2011.6090983.
Der volle Inhalt der QuelleAnegondi, Neha, Qi Yang, Michael Kawczynski, Verena Steffen und Simon S. Gao. „Predicting geographic atrophy growth rate from fundus autofluorescence images using deep neural networks“. In Multimodal Biomedical Imaging XVI, herausgegeben von Fred S. Azar, Xavier Intes und Qianqian Fang. SPIE, 2021. http://dx.doi.org/10.1117/12.2575898.
Der volle Inhalt der QuellePeralta-Ildefonso, Martha J., Ernesto Moya-Albor, Jorge Brieva, Esmeralda Lira-Romero, Andric C. Perez-Ortiz, Ramon Coral-Vazquez und Francisco J. Estrada-Mena. „Nuclear density analysis in microscopic images for the characterization of retinal geographic atrophy“. In 15th International Symposium on Medical Information Processing and Analysis, herausgegeben von Jorge Brieva, Eduardo Romero und Natasha Lepore. SPIE, 2020. http://dx.doi.org/10.1117/12.2542061.
Der volle Inhalt der QuelleDong, Jiwen, Junting Chen, Xizhan Gao, Rongbin Xu und Sijie Niu. „Automated geographic atrophy segmentation with multi-loss for SD-OCT images based on patient independent“. In Twelfth International Conference on Graphics and Image Processing, herausgegeben von Zhigeng Pan und Xinhong Hei. SPIE, 2021. http://dx.doi.org/10.1117/12.2589371.
Der volle Inhalt der QuelleLee, Noah, Andrew F. Laine und R. Theodore Smith. „A hybrid segmentation approach for geographic atrophy in fundus auto-fluorescence images for diagnosis of age-related macular degeneration“. In 2007 29th Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2007. http://dx.doi.org/10.1109/iembs.2007.4353455.
Der volle Inhalt der QuelleZhang, Yuhan, Zexuan Ji, Sijie Niu, Theodore Leng, Daniel L. Rubin und Qiang Chen. „A Multi-Scale Deep Convolutional Neural Network For Joint Segmentation And Prediction Of Geographic Atrophy In SD-OCT Images“. In 2019 IEEE 16th International Symposium on Biomedical Imaging (ISBI). IEEE, 2019. http://dx.doi.org/10.1109/isbi.2019.8759253.
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