Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Debbie S. Kuo"'
Autor:
Frank L. Brodie, Evan Kalin-Hajdu, Debbie S. Kuo, Kristin E. Hirabayashi, Reza Vagefi, Robert C. Kersten
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 1, Iss C, Pp 8-10 (2016)
Purpose: To describe a complication of retrobulbar amphotericin B injections in the treatment of invasive rhino-orbital asperigillosis. Observations: 27 year-old renal transplant recipient presented with a two-week history of headache, binocular dipl
Externí odkaz:
https://doaj.org/article/de6886100902492295a97aa25924f631
Autor:
Xueling Zhang, Weijia Dai, Xiuzhi Zhang, Lin Xie, Xiaoming Duan, Feng Wang, Yufang Su, Wei Liu, Xuemei Wang, Peng Lu, Jingmin Li, Guijun Xie, Liuzhi Zeng, Jianlu Gao, Aiping Zhao, Hongbo Qu, Ning Li, Ningli Wang, Jingni Yu, Yihua Zhu, Debbie S. Kuo, Min Zhu, Ping Liu, Xiang Ma, Junhong Zhao, Chunmei Zhao, Danyan Liu, Liang Liang, Li Tang, Jianping Hu, Jinqiang Yu, Sujie Fan, Hui Zhang, Hua Zhong, Kaijun Li, Liang Li, Jing Liang, Yanbing Qu, Hui Wang, Aiwu Fang, Gang Zhai, Hongying Cai, Haijun Li, Jing Song, Ying Su, Chunyan Qiao, Yong Zhang, Min Yu, Min Zhang, Bo Qu, Xuyang Liu, Guangxian Tang, Yuyan Zhang, Xiaobin Xie, Shaoping Ha, Yajuan Zheng, Hongbin Lyu, Xuanchu Duan, Zhihong Wu, Kai Cao, Hongyan Jia, Zuohong Wu, Yinong Zhang, Sumian Cheng, Fanglei Yu
Publikováno v:
Canadian Journal of Ophthalmology. 56:299-306
Objective To analyze the rates of blindness with the demographics and clinical characteristics of patients with primary angle-closure disease (PACD) to provide a comprehensive epidemiologic reference in China. Methods A retrospective analysis was con
Autor:
Debbie S Kuo, Jared T Sokol, Peter J Minogue, Viviana M Berthoud, Anne M Slavotinek, Eric C Beyer, Douglas B Gould
Publikováno v:
PLoS ONE, Vol 12, Iss 8, p e0183438 (2017)
Congenital cataracts occur in isolation in about 70% of cases or are associated with other abnormalities such as anterior segment dysgenesis and microphthalmia. We identified a three-generation family in the University of California San Francisco gla
Externí odkaz:
https://doaj.org/article/4bbde1caace64bfd879f29e94a35a995
Autor:
Sanjay Asrani, Debbie S. Kuo
Publikováno v:
Journal of glaucoma. 26(4)
Purpose Optical coherence tomography (OCT) has become an important tool in the diagnosis and management of glaucoma; however, there can be overlap in the OCT findings between glaucoma and other diseases. We describe the clinical examination finings a
Autor:
Peter J. Minogue, Eric C. Beyer, Jared T. Sokol, Debbie S. Kuo, Viviana M. Berthoud, Anne Slavotinek, Douglas B. Gould
Publikováno v:
PloS one, vol 12, iss 8
PLoS ONE
PLoS ONE, Vol 12, Iss 8, p e0183438 (2017)
PLoS ONE
PLoS ONE, Vol 12, Iss 8, p e0183438 (2017)
Author(s): Kuo, Debbie S; Sokol, Jared T; Minogue, Peter J; Berthoud, Viviana M; Slavotinek, Anne M; Beyer, Eric C; Gould, Douglas B | Abstract: PurposeCongenital cataracts occur in isolation in about 70% of cases or are associated with other abnorma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d57114f46b62253921bd3a0fe1006ed8
https://escholarship.org/uc/item/5x99q7m4
https://escholarship.org/uc/item/5x99q7m4
Publikováno v:
Experimental Eye Research. 111:17-26
A small percentage of retinal ganglion cells (RGCs) express melanopsin and are intrinsically photosensitive (ipRGCs). Whether light can affect the development of ipRGCs is not clear. In the rat retina, we found constant light exposure during the firs
Autor:
Jay M. Stewart, Robert B. Bhisitkul, Debbie S. Kuo, Bennie H. Jeng, Jacque L. Duncan, Yvonne Ou, Ying Han
Publikováno v:
Kuo, DS; Ou, Y; Jeng, BH; Bhisitkul, R; Stewart, JM; Duncan, JL; et al.(2014). Correlation of Serial Scleral and Corneal Pneumatonometry. Ophthalmology. doi: 10.1016/j.ophtha.2015.05.033. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/7n68v0gf
© 2015 American Academy of Ophthalmology. Purpose: To evaluate the usefulness of scleral pneumatonometry as an alternative for corneal measurements of intraocular pressure (IOP) over a broad range of IOPs. Design: Prospective, observational cohort s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c3a782a054115269775eb2657e33043
http://www.escholarship.org/uc/item/7n68v0gf
http://www.escholarship.org/uc/item/7n68v0gf
Autor:
Jack Favor, Mao Mao, Cassandre Labelle-Dumais, Jennifer M. Allen, Debbie S. Kuo, Douglas B. Gould, William B. Kauffman, Marion Jeanne
Publikováno v:
Hum. Mol. Genet. 23, 1709-1722 (2014)
Human Molecular Genetics
Human Molecular Genetics
Collagen type IV alpha 1 and 2 (COL4A1 and COL4A2) are present in nearly all basement membranes. COL4A1 and COL4A2 mutations are pleiotropic, affecting multiple organ systems to differing degrees, and both genetic-context and environmental factors in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a0af2df1338f7bb27f2154b2856cd2e
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=28953
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=28953
Publikováno v:
Human molecular genetics, vol 21, iss R1
Human Molecular Genetics
Kuo, DS; Labelle-Dumais, C; & Gould, DB. (2012). COL4A1 and COL4A2 mutations and disease: insights into pathogenic mechanisms and potential therapeutic targets. HUMAN MOLECULAR GENETICS, 21, R97-R110. doi: 10.1093/hmg/dds346. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/8586m9bx
Human Molecular Genetics
Kuo, DS; Labelle-Dumais, C; & Gould, DB. (2012). COL4A1 and COL4A2 mutations and disease: insights into pathogenic mechanisms and potential therapeutic targets. HUMAN MOLECULAR GENETICS, 21, R97-R110. doi: 10.1093/hmg/dds346. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/8586m9bx
Heterotrimers composed of collagen type IV alpha 1 (COL4A1) and alpha 2 (COL4A2) constitute one of the most abundant components of nearly all basement membranes. Accordingly, mutations in COL4A1 or COL4A2 are pleiotropic and contribute to a broad spe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20825ae1a5b81a23263b78ddd67ed3a3
https://escholarship.org/uc/item/8586m9bx
https://escholarship.org/uc/item/8586m9bx
Autor:
Jan C. den Hollander, Grazia M.S. Mancini, Elly Verbeek, Rachel Schot, René de Coo, Jeroen Dudink, Maarten H. Lequin, Cathryn J. Poulton, Frans W. Verheijen, Daniel J. Licht, Debbie S. Kuo, Renske Oegema, Douglas B. Gould, Marije E.C. Meuwissen, Dicky J. Halley, Paul Govaert
Publikováno v:
European Journal of Human Genetics, 20(8), 844-851. Nature Publishing Group
Familial porencephaly, leukoencephalopathy and small-vessel disease belong to the spectrum of disorders ascribed to dominant mutations in the gene encoding for type IV collagen alpha-1 (COL4A1). Mice harbouring mutations in either Col4a1 or Col4a2 su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc0033c65d161aa8341e7ac17720f2aa
https://pure.eur.nl/en/publications/a78483a2-8596-4c72-beb4-8e1dc0bc922f
https://pure.eur.nl/en/publications/a78483a2-8596-4c72-beb4-8e1dc0bc922f