Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Masako Chen"'
Autor:
Carl S. Wilkins, Masako Chen, Gaurav Chandra, Thomas O. Muldoon, Paul A. Sidoti, C. Michael Samson, Richard B. Rosen
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 27, Iss , Pp 101572- (2022)
Purpose: To describe a case of late post-surgical sympathetic ophthalmia documented with multimodal imaging. Observations: A 74-year-old male presented to the urgent care of the New York Eye and Ear Infirmary with blurry vision and discomfort in his
Externí odkaz:
https://doaj.org/article/9b484adcd9b14202a2aa026ca88d05e5
Autor:
Sierra Jin, Tahsin Khundkar, Masako Chen, Charles G. Miller, Daniel J. Polla, Harsha S Reddy, Archana A Nair, Ethan K Sobol, Royce W.S. Chen, Carolina Adams, Jamie B. Rosenberg, Duaa Sharfi, Stephanie B Engelhard, Alcina Lidder, Sarah A. Avila
Publikováno v:
Current Opinion in Ophthalmology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fc3b5227542c41d13f1d059154a9dd0
https://pubmed.ncbi.nlm.nih.gov/32694269
https://pubmed.ncbi.nlm.nih.gov/32694269
Autor:
Russell R. Lonser, Roscoe O. Brady, Masako Chen, Donald Y. Ye, Chunzhang Yang, Zhengping Zhuang, Jie Lu
Publikováno v:
Proceedings of the National Academy of Sciences. 108:21200-21205
Gaucher disease (GD) is caused by a spectrum of genetic mutations within the gene encoding the lysosomal enzyme glucocerebrosidase (GCase). These mutations often lead to misfolded proteins that are recognized by the unfolded protein response system a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::938c3c1e19a88cb454f872a109d385ed
https://doi.org/10.1073/pnas.1119181109
https://doi.org/10.1073/pnas.1119181109
Autor:
Chunzhang Yang, Christine R. Kaneski, Russell R. Lonser, Richard J. Hodes, Jie Lu, Roscoe O. Brady, David S. Xu, Zhengping Zhuang, Eli Thompson, Masako Chen, Rajiv R. Iyer, Jeffrey Chiang
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 107(50)
Gaucher disease (GD), the most common lysosomal storage disorder of humans, is caused by mutations in the gene coding for the enzyme glucocerebrosidase (GCase). Clinical manifestations vary among patients with the three types of GD, and phenotypic he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31aae3cac4e0492159c4d5570d5e9ead
https://pubmed.ncbi.nlm.nih.gov/21098288
https://pubmed.ncbi.nlm.nih.gov/21098288
Autor:
Jie Lu, Chunzhang Yang, Masako Chen, Ye, Donald Y., Lonser, Russell R., Brady, Roscoe O., Zhengping Zhuang
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America; 12/27/2011, Vol. 108 Issue 52, p21200-21205, 6p