Zobrazeno 1 - 10
of 168
pro vyhledávání: '"Preising, M"'
Autor:
Petzold, A., Albrecht, P., Balcer, L., Bekkers, E., Brandt, A. U., Calabresi, P. A., Deborah, O. G., Graves, J. S., Green, A., Keane, P. A., Nij Bijvank, J. A., Sander, J. W., Paul, F., Saidha, S., Villoslada, P., Wagner, S. K., Yeh, E. A., Aktas, O., Antel, J., Asgari, N., Audo, I., Avasarala, J., Avril, D., Bagnato, F. R., Banwell, B., Bar-Or, A., Behbehani, R., Manterola, A. B., Bennett, J., Benson, L., Bernard, J., Bremond-Gignac, D., Britze, J., Burton, J., Calkwood, J., Carroll, W., Chandratheva, A., Cohen, J., Comi, G., Cordano, C., Costa, S., Costello, F., Courtney, A., Cruz-Herranz, A., Cutter, G., Crabb, D., Delott, L., De Seze, J., Diem, R., Dollfuss, H., El Ayoubi, N. K., Fasser, C., Finke, C., Fischer, D., Fitzgerald, K., Fonseca, P., Frederiksen, J. L., Frohman, E., Frohman, T., Fujihara, K., Cuellar, I. G., Galetta, S., Garcia-Martin, E., Giovannoni, G., Glebauskiene, B., Suarez, I. G., Jensen, G. P., Hamann, S., Hartung, H. -P., Havla, J., Hemmer, B., Huang, S. -C., Imitola, J., Jasinskas, V., Jiang, H., Kafieh, R., Kappos, L., Kardon, R., Keegan, D., Kildebeck, E., Kim, U. S., Klistorner, S., Knier, B., Kolbe, S., Korn, T., Krupp, L., Lagreze, W., Leocani, L., Levin, N., Liskova, P., Preiningerova, J. L., Lorenz, B., May, E., Miller, D., Mikolajczak, J., Said, S. M., Montalban, X., Morrow, M., Mowry, E., Murta, J., Navas, C., Nolan, R., Nowomiejska, K., Oertel, F. C., Oh, J., Oreja-Guevara, C., Orssaud, C., Osborne, B., Outteryck, O., Paiva, C., Palace, J., Papadopoulou, A., Patsopoulos, N., Pontikos, N., Preising, M., Prince, J., Reich, D., Rejdak, R., Ringelstein, M., Rodriguez de Antonio, L., Sahel, J. -A., Sanchez-Dalmau, B., Sastre-Garriga, J., Schippling, S., Schuman, J., Shindler, K., Shin, R., Shuey, N., Soelberg, K., Specovius, S., Suppiej, A., Thompson, A., Toosy, A., Torres, R., Touitou, V., Trauzettel-Klosinski, S., van der Walt, A., Vermersch, P., Vidal-Jordana, A., Waldman, A. T., Waters, C., Wheeler, R., White, O., Wilhelm, H., Winges, K. M., Wiegerinck, N., Wiehe, L., Wisnewski, T., Wong, S., Wurfel, J., Yaghi, S., You, Y., Yu, Z., Yu-Wai-Man, P., Zemaitien≐, R., Zimmermann, H.
Publikováno v:
Petzold, A, Albrecht, P, Balcer, L, Bekkers, E, Brandt, A U, Calabresi, P A, Deborah, O G, Graves, J S, Green, A, Keane, P A, Nij Bijvank, J A, Sander, J W, Paul, F, Saidha, S, Villoslada, P, Wagner, S K, Yeh, E A & the IMSVISUAL, ERN-EYE Consortium 2021, ' Artificial intelligence extension of the OSCAR-IB criteria ', Annals of Clinical and Translational Neurology, vol. 8, no. 7, pp. 1528-1542 . https://doi.org/10.1002/acn3.51320
the IMSVISUAL, ERN-EYE Consortium 2021, ' Artificial intelligence extension of the OSCAR-IB criteria ', Annals of Clinical and Translational Neurology, vol. 8, no. 7, pp. 1528-1542 . https://doi.org/10.1002/acn3.51320
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology, Vol 8, Iss 7, Pp 1528-1542 (2021)
the IMSVISUAL, ERN-EYE Consortium 2021, ' Artificial intelligence extension of the OSCAR-IB criteria ', Annals of Clinical and Translational Neurology, vol. 8, no. 7, pp. 1528-1542 . https://doi.org/10.1002/acn3.51320
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology, Vol 8, Iss 7, Pp 1528-1542 (2021)
Artificial intelligence (AI)‐based diagnostic algorithms have achieved ambitious aims through automated image pattern recognition. For neurological disorders, this includes neurodegeneration and inflammation. Scalable imaging technology for big dat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab75a15c7ed188859f7ddc8d47650216
https://openaccess.city.ac.uk/id/eprint/26361/1/acn3.51320.pdf
https://openaccess.city.ac.uk/id/eprint/26361/1/acn3.51320.pdf
Autor:
Holz, Frank G., Lorenz, B., Scholz, J.P., K��pper, K., Wirtz, L., Cavriani, N., Brinken, R., Preising, M., Herrmann, P.
Publikováno v:
184. Versammlung des Vereins Rheinisch-Westfälischer Augenärzte; 20220128-20220129; Bielefeld; DOC22rwa05 /20220128/
Ziel: Seit kurzem steht die subretinale Gentherapie mit Voretigen Neparvovec (VN, LuxturnaTM) bei Patienten mit IRD (Inherited Retinal Degeneration) durch biallelische Mutationen in RPE65 zur Verf��gung. Wir berichten ��ber die chirurgischen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c3725ba920bcd010db0bcb42cc9cf14
Publikováno v:
BioMed Research International. 5/23/2018, Vol. 2018, p1-11. 11p.
Akademický článek
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Akademický článek
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Autor:
Sergouniotis, Panagiotis I., Maxime, Emmanuel, Leroux, Dorothée, Olry, Annie, Thompson, Rachel, Rath, Ana, Robinson, Peter N., Dollfus, Hélèneashworth, Jl, Audo, I, Balciuniene, Vj, Banin, E, Black, Gc, Böhringer, D, Boon, Cjf, Bremond-Gignac, D, Calvas, P, Castela, G, Dagnelie, G, Dollfus, H, Downes, Sm, Fasolo, A, Fasser, C, Gelzinis, A, Goetz, K, Hamann, S, Héon, E, Iarossi, G, Kawasaki, A, Keegan, D, Kessel, L, Khan, K, Klett, A, Köhler, S, Leroux, D, Leroy, Bp, Lisch, W, Liskova, P, Lorenz, B, Maggi, R, Maxime, E, Meunier, I, Mohand-Said, S, Nowomiejska, K, Perdomo, Y, Petzold, A, Preising, M, Robinson, Pn, Scholl, Hpn, Sergouniotis, Pi, Sodi, A, Stingl, K, Studer, F, Suppiej, A, Thompson, R, Touitou, V, Traboulsi, E, Trumpaitis, J, Tuft, Sj, Vaclavik, V, Valeina, S, Van Cauwenbergh, C, Verloes, A, Vighetto, A, Wheeler, R, Wheeler-Schilling, T, Yu-Wai-Man, P, Zobor, D, Zrenner, E.
Publikováno v:
ERN-EYE Ontology Study Group 2019, ' An ontological foundation for ocular phenotypes and rare eye diseases ', Orphanet Journal of Rare Diseases, vol. 14, no. 1, pp. 8 . https://doi.org/10.1186/s13023-018-0980-6
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 14
Orphanet Journal of Rare Diseases, 2019, 14 (8), pp.1-5. ⟨10.1186/s13023-018-0980-6⟩
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-5 (2019)
Sergouniotis, P I, Maxime, E, Leroux, D, Olry, A, Thompson, R, Rath, A, Robinson, P N, Dollfus, H, ERN-EYE Ontology Study Group, Ashworth, J L, Audo, I, Balciuniene, V J, Hamann, S, Kessel, L, Yu-Wai-Man, P, Zobor, D & Zrenner, E 2019, ' An ontological foundation for ocular phenotypes and rare eye diseases ', Orphanet Journal of Rare Diseases, vol. 14, 8 . https://doi.org/10.1186/s13023-018-0980-6
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 14
Orphanet Journal of Rare Diseases, 2019, 14 (8), pp.1-5. ⟨10.1186/s13023-018-0980-6⟩
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-5 (2019)
Sergouniotis, P I, Maxime, E, Leroux, D, Olry, A, Thompson, R, Rath, A, Robinson, P N, Dollfus, H, ERN-EYE Ontology Study Group, Ashworth, J L, Audo, I, Balciuniene, V J, Hamann, S, Kessel, L, Yu-Wai-Man, P, Zobor, D & Zrenner, E 2019, ' An ontological foundation for ocular phenotypes and rare eye diseases ', Orphanet Journal of Rare Diseases, vol. 14, 8 . https://doi.org/10.1186/s13023-018-0980-6
Background The optical accessibility of the eye and technological advances in ophthalmic diagnostics have put ophthalmology at the forefront of data-driven medicine. The focus of this study is rare eye disorders, a group of conditions whose clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::840fa6905fa94a0e7ca88a0762068559
https://doi.org/10.1186/s13023-018-0980-6
https://doi.org/10.1186/s13023-018-0980-6
Publikováno v:
European Journal of Clinical Nutrition. Jun2016, Vol. 70 Issue 6, p656-661. 6p. 5 Charts.
Autor:
Leroux, D., Dollfus, H., Ashworth, J., Black, G., Bohringer, D., Boon, C.J., Cremers, F., Daly, A., Fasser, C., Fischer, D., Keegan, D., Khan, K., Larkin, F., Larsen, M., Leroy, B.P., Liskova, P., Lorenz, B., Martinho, C., Mohand-Said, S., Petzold, A., Preising, M., Reinhart, T., Wheeler-Schilling, T., Wong, S., Zrenner, E., All ERN-EYE Members
Publikováno v:
European Journal of Human Genetics, 26, 804-805
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a01daaedaa4b20cacf99748afcf8efff
http://hdl.handle.net/1887/96576
http://hdl.handle.net/1887/96576
Autor:
Valkenburg, D, Van Cauwenbergh, C, Lorenz, B, van Genderen, MM, Bertelsen, M, Pott, JWR, Coppieters, F, de Zaeytijd, J, Thiadens, Alberta, Klaver, Caroline, Kroes, HY, van Schooneveld, MJ, Preising, M, Hoyng, CB, Leroy, BP, van den Born, LI, Collin, RWJ
Publikováno v:
Investigative ophthalmology & visual science, 59(11), 4384-4391. ASSOC RESEARCH VISION OPHTHALMOLOGY INC
Investigative Ophthalmology & Visual Science, 59(11), 4384-4391. Association for Research in Vision and Ophthalmology Inc.
Investigative Ophthalmology & Visual Science, 59(11), 4384-4391. Association for Research in Vision and Ophthalmology Inc.
Purpose: To describe the phenotypic spectrum of retinal disease caused by the c.2991+1655A>G mutation in CEP290 and to compare disease severity between homozygous and compound heterozygous patients. Methods: Medical records were reviewed for best-cor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::429fee8cc61cdf454e20b62f3349544b
https://research.rug.nl/en/publications/f5244a69-f673-4271-b231-e90826dca1a6
https://research.rug.nl/en/publications/f5244a69-f673-4271-b231-e90826dca1a6
Autor:
Guerriero, S.1 silvanaguerriero@gmail.com, Preising, M. N.2, Ciccolella, N.1, Causio, F.3, Lorenz, B.2, Fischetto, R.4
Publikováno v:
Ophthalmologica. Apr2011, Vol. 225 Issue 4, p228-235. 8p. 1 Color Photograph, 1 Black and White Photograph, 1 Diagram, 1 Chart.