Liu HC - Search Results

1

[Association of calcium-sensing receptor gene polymorphism with serum calcium level in healthy young Han women in Beijing].

Wang O, Meng XW, Xing XP, Xia WB, Li M, Xu L, Zhou XY, Jiao J, Hu YY, Liu HC. Wang O, et al. Among authors: liu hc. Zhonghua Nei Ke Za Zhi. 2007 Jan;46(1):43-7. Zhonghua Nei Ke Za Zhi. 2007. PMID: 17331389 Chinese.

2

Clinical phenotypes of Chinese primary hyperparathyroidism patients are associated with the calcium-sensing receptor gene R990G polymorphism.

Han G, Wang O, Nie M, Zhu Y, Meng X, Hu Y, Liu H, Xing X. Han G, et al. Eur J Endocrinol. 2013 Oct 1;169(5):629-38. doi: 10.1530/EJE-13-0441. Print 2013 Nov. Eur J Endocrinol. 2013. PMID: 23946278

3

[The effects of continuous stimulation with different doses of parathyroid hormone 1-34 fragment on human SaoS-2 cells].

Li M, Meng XW, Zhou XY, Xing XP, Liu HC. Li M, et al. Among authors: liu hc. Zhonghua Nei Ke Za Zhi. 2003 Mar;42(3):177-80. Zhonghua Nei Ke Za Zhi. 2003. PMID: 12816700 Chinese.

4

[Skeletal biomechanical properties improvement in ovariectomized osteoporotic rats of teriparatide was retarded by alendronate].

Li M, Jiao J, Meng XW, Zhou XY, Xing XP, Xia WB, Wang O, Jiang Y, Liu HC, Hu YY. Li M, et al. Among authors: liu hc. Zhonghua Nei Ke Za Zhi. 2006 Feb;45(2):104-7. Zhonghua Nei Ke Za Zhi. 2006. PMID: 16624115 Chinese.

5

[The efficacy and safety of intravenous bisphosphonates in the treatment of primary hyperparathyroidism complicated by hypercalcemia crisis].

Han GY, Wang O, Xing XP, Meng XW, Lian XL, Guan H, Ye W, Xia WB, Li M, Jiang Y, Hu YY, Liu HC, Cui QC. Han GY, et al. Among authors: liu hc. Zhonghua Nei Ke Za Zhi. 2009 Sep;48(9):729-33. Zhonghua Nei Ke Za Zhi. 2009. PMID: 20079207 Chinese.

6

Germinal mosaicism of GATA3 in a family with HDR syndrome.

Sun Y, Xia W, Xing X, Li M, Wang O, Jiang Y, Pei Y, Ye P, Liu H, Hu Y, Meng X, Zhou X. Sun Y, et al. Am J Med Genet A. 2009 Feb 15;149A(4):776-8. doi: 10.1002/ajmg.a.32706. Am J Med Genet A. 2009. PMID: 19253381 No abstract available.

7

A recurrent mutation c.617G>A in the ACVR1 gene causes fibrodysplasia ossificans progressiva in two Chinese patients.

Sun Y, Xia W, Jiang Y, Xing X, Li M, Wang O, Zhang H, Hu Y, Liu H, Meng X, Zhou X. Sun Y, et al. Calcif Tissue Int. 2009 May;84(5):361-5. doi: 10.1007/s00223-009-9235-9. Epub 2009 Mar 20. Calcif Tissue Int. 2009. PMID: 19300893

8

FGF23 analysis of a Chinese family with autosomal dominant hypophosphatemic rickets.

Sun Y, Wang O, Xia W, Jiang Y, Li M, Xing X, Hu Y, Liu H, Meng X, Zhou X. Sun Y, et al. J Bone Miner Metab. 2012 Jan;30(1):78-84. doi: 10.1007/s00774-011-0285-5. Epub 2011 Jun 28. J Bone Miner Metab. 2012. PMID: 21710177

9

Novel mutations of CYP27B1 gene lead to reduced activity of 1α-hydroxylase in Chinese patients.

Cui N, Xia W, Su H, Pang L, Jiang Y, Sun Y, Nie M, Xing X, Li M, Wang O, Yuan T, Chi Y, Hu Y, Liu H, Meng X, Zhou X. Cui N, et al. Bone. 2012 Sep;51(3):563-9. doi: 10.1016/j.bone.2012.05.006. Epub 2012 May 12. Bone. 2012. PMID: 22588163

10

[Evaluation of bone architecture and biomechanic properties by peripheral quantitative computed tomography in rats].

Xing XP, Xia WB, Meng XW, Zhou XY, Hu YY, Liu HC. Xing XP, et al. Among authors: liu hc. Zhonghua Yi Xue Za Zhi. 2003 May 10;83(9):791-5. Zhonghua Yi Xue Za Zhi. 2003. PMID: 12899761 Chinese.

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