Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Hong-wen Zhou"'
Publikováno v:
BMC Nephrology, Vol 18, Iss 1, Pp 1-10 (2017)
Abstract Background Association between metabolic syndrome (MS) and mildly reduced estimated glomerular filtration rates (eGFRs) remains unclear. Therefore, we aimed to evaluate the association between MS and a mildly reduced eGFR in Chinese adults.
Externí odkaz:
https://doaj.org/article/044d2711b8b4468a94a3556b318cbe3f
Autor:
Hong-Qi Fan, Wei Tang, Zhi-Xiao Wang, Su-Juan Wang, Yue-Hua Qin, Qi Fu, Yuan Gao, Min Sun, Mei Zhang, Hong-Wen Zhou, Tao Yang
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e67759 (2013)
ObjectiveTo examine whether serum uric acid (SUA) is associated with 2-hour postload glucose (2-h PG) in Chinese with impaired fasting plasma glucose (IFG) and/or HbA1c (IA1C).Research design and methodsAnthropometric and biochemical examinations, su
Externí odkaz:
https://doaj.org/article/a27cac1a90354147a559903c1e34a2de
Publikováno v:
Yi chuan = Hereditas. 44(10)
Congenital generalized lipodystrophy (CGL) is an extremely rare genetic disease mainly characterized by absence of whole-body adipose tissue and metabolic dysfunctions such as insulin resistance, diabetes mellitus, hypertriglyceridemia, hepatic steat
Publikováno v:
Yi chuan = Hereditas. 44(10)
Glucose metabolism plays a central role in energy supply and metabolism regulation in various tissues and organs. Besides, insulin is the sole hormone lowering blood glucose in the body, and islet function and insulin sensitivity are the key steps mo
Publikováno v:
Yi chuan = Hereditas. 44(9)
Congenital hyperinsulinemia (CHI) is a disease phenotype characterized by persistent or recurrent hypoglycemia due to abnormal secretion of insulin by β cells of the pancreas. CHI induced by activation mutation of a single allele of glucokinase (GCK
Publikováno v:
Clinical endocrinologyREFERENCES. 97(6)
A direct evaluation of insulin sensitivity on pituitary response to gonadotropin relasing hormone (GnRH) has not been shown in congenital hypogonadotropic hypogonadism (CHH), despite a growing body of evidence in the association of testosterone conce
Autor:
Wan-Zi, Jiang, Li-Wen, Zhang, Cai-Hong, He, Mei-Hua, Ruan, Yong, Ji, Jian-Rong, Yu, Hong-Wen, Zhou
Publikováno v:
Yi chuan = Hereditas. 43(11)
Familial hypercholesterolemia (FH) is an autosomal inherited disease characterized by a significant increase in low density lipoprotein cholesterol (LDL-C), tendon xanthoma and premature coronary artery disease (PCAD). In this paper, we analyze the c
Publikováno v:
Yi chuan = Hereditas. 43(6)
Rare diseases refer to diseases with low incidence. Currently, there are over 8000 rare diseases in the world. Effective prevention and treatment of rare diseases is an important part of 'healthy China'. In this paper, status and drug development of
Publikováno v:
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
BACKGROUND Clinical cases of nonmedullary thyroid carcinoma (NMTC) in combination with primary hyperparathyroidism (PHPT) have been reported occasionally. However, the clinical characteristics and risk factors of concomitant NMTC in PHPT patients rem
Publikováno v:
Applied Mechanics and Materials. :756-760
The multi-hazard, wide-covered, complex factors during the large complex underground construction process pose severe challenges to the construction project. With the help of successful forecast cases, typical geological interpretation signs, optimiz