Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Cai-ni Fan"'
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 10, Iss 2, Pp 253-256 (2010)
DOI:10.3969/j.issn.1672-6731.2010.02.022
Externí odkaz:
https://doaj.org/article/a3c39d880c4f41b0a0a539d661d2ec26
Publikováno v:
Clinical Hypertension
Clinical Hypertension, Vol 25, Iss 1, Pp 1-9 (2019)
Clinical Hypertension, Vol 25, Iss 1, Pp 1-9 (2019)
Background 17α-hydroxylase deficiency is a rare autosomal recessive disorder caused by mutations in the cytochrome P450 family 17 subfamily A member 1 gene. The major clinical presentation includes hypertension, hypokalemia, male pseudohermaphroditi
Publikováno v:
RSC advances. 9(58)
PtPd nanoflowers (PtPd NFs) exhibit intrinsic peroxidase-like activity as nanozymes, but the nanozymes lack substrate specificity and have low catalytic activity. Herein, a molecularly imprinted nanogel on PtPd NFs was prepared by using 3,3′,5,5′
Publikováno v:
American Journal of Hypertension. 33:581-581
Background To study the correlation between blood pressure variability (BPV) and plasma renin activity (PRA), angiotensin II (AngII), aldosterone levels in patients with essential hypertension. Methods A total of 300 patients with mild to moderate es
Autor:
Man He-lian, Dan-dan Tian, Shan-shan Wang, Hai-ying Zhao, Ling Jiang, Fan-shen Meng, Cai-ni Fan, Xin-yu Wang, Wang Meng-lin, Shu-xian Cui, Min Liu, Hao Wang, Ling Li
Publikováno v:
Journal of Hypertension. 36:e181
Autor:
Cai-ni Fan, Min Liu, Ling Li, Man He-lian, Dan-dan Tian, Fan-shen Meng, Hai-ying Zhao, Meng-lin Wang, Guang-zhi Liu, Jian-qin Gu, Shan-shan Wang, Ling Jiang, Wang Hao, Shu-xian Cui
Publikováno v:
Journal of Hypertension. 36:e306
Autor:
Cai-ni Fan, Yan-Yan Song, Jianqing Ding, Jian-Fang Ma, Guo-Yuan Yang, Xiao-Yu Xin, Sheng-Di Chen
Publikováno v:
Thrombosis Research. 124:619-624
Introduction Genetic studies restricted to young adult ischemic stroke patients may help in excluding the potentially confounding variables encountered with advanced age; thus, allowing a more precise risk evaluation derived from the inherited mutati