Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Minzhuang Lin"'
Autor:
Ruiming Cai, Minzhuang Lin, Zhiyong Chen, Yongtong Lai, Xianen Huang, Guozhi Zhao, Xuekun Guo, Zhongtang Xiong, Juan Chen, Hui Chen, Qingping Jiang, Shaoyan Liu, Yuexin Yang, Weixiang Liang, Minhui Zou, Tao Liu, Wenfang Chen, Hongzhou Liu, Juan Peng
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-11 (2019)
Abstract Background Primary hyperoxaluria (PH) is a rare inborn disorder of the metabolism of glyoxylate, which causes the hallmark production oxalate and forms insoluble calcium oxalate crystals that accumulate in the kidney and other organs. Since
Externí odkaz:
https://doaj.org/article/2dba2769d63542628d3ad7342834b28c
Autor:
Wenfang Chen, Juan Chen, Guozhi Zhao, Xuekun Guo, Minzhuang Lin, Qingping Jiang, Hongzhou Liu, Yongtong Lai, Hui Chen, Yuexin Yang, Weixiang Liang, Tao Liu, Shaoyan Liu, Minhui Zou, Xianen Huang, Juan Peng, Zhongtang Xiong, Ruiming Cai, Zhiyong Chen
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-11 (2019)
BMC Nephrology
BMC Nephrology
Background Primary hyperoxaluria (PH) is a rare inborn disorder of the metabolism of glyoxylate, which causes the hallmark production oxalate and forms insoluble calcium oxalate crystals that accumulate in the kidney and other organs. Since the manif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f15f3d2d51fada52b5c940c4ef32e0b
http://link.springer.com/article/10.1186/s12882-019-1402-2
http://link.springer.com/article/10.1186/s12882-019-1402-2