المؤلفون: Aung, Tin, Ozaki, Mineo, Lee, Mei, Schlötzer-Schrehardt, Ursula, Thorleifsson, Gudmar, Mizoguchi, Takanori, Igo, Robert, Haripriya, Aravind, Williams, Susan, Astakhov, Yury, Orr, Andrew, Burdon, Kathryn, Nakano, Satoko, Mori, Kazuhiko, Abu-Amero, Khaled, Hauser, Michael, Li, Zheng, Prakadeeswari, Gopalakrishnan, Bailey, Jessica, Cherecheanu, Alina, Kang, Jae, Nelson, Sarah, Hayashi, Ken, Manabe, Shin-Ichi, Kazama, Shigeyasu, Zarnowski, Tomasz, Inoue, Kenji, Irkec, Murat, Coca-Prados, Miguel, Sugiyama, Kazuhisa, Järvelä, Irma, Schlottmann, Patricio, Lerner, S, Lamari, Hasnaa, Nilgün, Yildirim, Bikbov, Mukharram, Park, Ki, Cha, Soon, Yamashiro, Kenji, Zenteno, Juan, Jonas, Jost, Kumar, Rajesh, Perera, Shamira, Chan, Anita, Kobakhidze, Nino, George, Ronnie, Vijaya, Lingam, Do, Tan, Edward, Deepak, de Juan Marcos, Lourdes, Pakravan, Mohammad, Moghimi, Sasan, Ideta, Ryuichi, Bach-Holm, Daniella, Kappelgaard, Per, Wirostko, Barbara, Thomas, Samuel, Gaston, Daniel, Bedard, Karen, Greer, Wenda, Yang, Zhenglin, Chen, Xueyi, Huang, Lulin, Sang, Jinghong, Jia, Hongyan, Jia, Liyun, Qiao, Chunyan, Zhang, Hui, Liu, Xuyang, Zhao, Bowen, Wang, Ya-Xing, Xu, Liang, Leruez, Stéphanie, Reynier, Pascal, Chichua, George, Tabagari, Sergo, Uebe, Steffen, Zenkel, Matthias, Berner, Daniel, Mossböck, Georg, Weisschuh, Nicole, Hoja, Ursula, Welge-Luessen, Ulrich-Christoph, Mardin, Christian, Founti, Panayiota, Chatzikyriakidou, Anthi, Pappas, Theofanis, Anastasopoulos, Eleftherios, Lambropoulos, Alexandros, Ghosh, Arkasubhra, Shetty, Rohit, Porporato, Natalia, Saravanan, Vijayan, Venkatesh, Rengaraj, Shivkumar, Chandrashekaran, Kalpana, Narendran, Sarangapani, Sripriya, Kanavi, Mozhgan, Beni, Afsaneh, Yazdani, Shahin

المصدر: Nature Genetics. 49(7)

مصطلحات موضوعية: Aged, 80 and over, Alleles, Amino Acid Oxidoreductases, Amino Acid Substitution, Asian People, Calcium Channels, Cell Adhesion, Exfoliation Syndrome, Extracellular Matrix, Eye, Female, Gene Expression Profiling, Genetic Predisposition to Disease, Genome-Wide Association Study, Haplotypes, Humans, Male, Molecular Chaperones, Mutation, Missense, Point Mutation, RNA, Messenger, Spheroids, Cellular

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/8v79f9zk

المؤلفون: Brynskov, Troels, Bach‐Holm, Daniella, Kappelgaard, Per, Siersma, Volkert, Pedersen, Karen Bjerg, Kessel, Line

المصدر: Acta Ophthalmologica (1755375X); Mar2024, Vol. 102 Issue 2, p228-237, 10p

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المؤلفون: Kappelgaard, Per, Hansen, Katrine B., Vilsbøll, Tina, Knop, Filip K., Larsen, Michael

المصدر: Documenta Ophthalmologica: The Journal of Clinical Electrophysiology and Vision - The Official Journal of the International Society for Clinical Electrophysiology and Vision. February 2012 124(1):49-57

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المؤلفون: Kessel, Line, Pedersen, Karen Bjerg, Siersma, Volkert, Kappelgaard, Per, Bach‐Holm, Daniella

المصدر: Acta Ophthalmologica (1755375X); Jun2021, Vol. 99 Issue 4, p362-368, 7p

مصطلحات موضوعية: CONGENITAL glaucoma, TRABECULECTOMY, OPERATIVE surgery, INTRAOCULAR pressure, SURGICAL diagnosis

مصطلحات جغرافية: DENMARK

المؤلفون: Kappelgaard, Per, Wolfram, Frauke, Hamann, Steffen

المصدر: Neuro-Ophthalmology; Feb2020, Vol. 44 Issue 1, p24-27, 4p

مصطلحات موضوعية: CAROTID artery dissections, HORNER syndrome, FETOFETAL transfusion, TWINS

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