Genotype and Long-term Clinical Course of Bietti Crystalline Dystrophy in Korean and Japanese Patients
Year: 2021
Type: article
Study design: Observational Study
Source: Ophthalmology Retina
Authors: Yusuke Murakami, Yoshito Koyanagi, Masatoshi Fukushima, Marika Yoshimura, Kohta Fujiwara, Masato Akiyama, Yukihide Momozawa, Shinji Ueno, Hiroko Terasaki, Akio Oishi, Manabu Miyata, Hanako Ikeda, Akitaka Tsujikawa, Kei Mizobuchi, Takaaki Hayashi, Kaoru Fujinami, Kazushige Tsunoda, Jun Young Park, Jinu Han, Min Kim, Christopher Seungkyu Lee, Sang Jin Kim, Tae Kwann Park, Kwangsic Joo, Se Joon Woo, Yasuhiro Ikeda, Koh-Hei Sonoda
Institutions: Kyushu University, RIKEN Center for Integrative Medical Sciences, Nagoya University, Nagasaki University, Kyoto University, Jikei University School of Medicine, Tokyo Medical Center, National Hospital Organization, Seoul National University, Seoul National University Bundang Hospital, Yonsei University, Gangnam Severance Hospital, Severance Hospital, Samsung Medical Center, Soonchunhyang University Hospital Bucheon, University of Miyazaki
Language: English
Subfield: Ophthalmology
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
Funders: Pfizer, Novartis, Meso Scale Diagnostics, Cell Science Research Foundation, Japan Agency for Medical Research and Development, Nihon Pharmaceutical, Seoul National University Bundang Hospital, National Research Foundation of Korea, Eisai, Santen, Astellas Pharma, Otsuka Pharmaceutical, Ono Pharmaceutical, Ministry of Science and ICT, South Korea, Novartis Pharma, Bayer Yakuhin, Japan Society for the Promotion of Science, Japan Science and Technology Agency, Korea Centers for Disease Control and Prevention, Janssen Pharmaceuticals
Awards: G1413124473, Pathological clarification and development of novel treatment in neovascular age-related macular degeneration using adaptive-optics optical coherence tomography, G1888717735, G3558516005, Pathological clarification and development of novel treatment in age-related macular degeneration by a multiple approach, Comprehensive genetic screening and establishment of novel therapeutic method in retinitis pigmentosa, Lipid profiles of retinal pigment epithelial cells and the mechanism of Drusen formation., Whole exome sequencing and identification of disease phenotypes for the treatment of progressive inherited retinal disorders
OpenAlex ID: W3131645009