Zhang MN - Search Results

1

A novel missense mutation, GGC(Arg454) --> TGC(Cys), of CYP11B1 gene identified in a Chinese family with steroid 11beta-hydroxylase deficiency.

Ye ZQ, Zhang MN, Zhang HJ, Jiang JJ, Li XY, Zhang KQ. Ye ZQ, et al. Among authors: zhang kq, zhang hj, zhang mn. Chin Med J (Engl). 2010 May 20;123(10):1264-8. Chin Med J (Engl). 2010. PMID: 20529578

2

Variations in the promoter of CYP21A2 gene identified in a Chinese patient with simple virilizing form of 21-hydroxylase deficiency.

Zhang HJ, Yang J, Zhang MN, Zhang W, Liu JM, Wang WQ, Ning G, Li XY. Zhang HJ, et al. Among authors: zhang w, zhang mn. Clin Endocrinol (Oxf). 2009 Feb;70(2):201-7. doi: 10.1111/j.1365-2265.2008.03356.x. Epub 2008 Aug 13. Clin Endocrinol (Oxf). 2009. PMID: 18702679

3

Seven novel DAX1 mutations with loss of function identified in Chinese patients with congenital adrenal hypoplasia.

Li N, Liu R, Zhang H, Yang J, Sun S, Zhang M, Liu Y, Lu Y, Wang W, Mu Y, Ning G, Li X. Li N, et al. J Clin Endocrinol Metab. 2010 Sep;95(9):E104-11. doi: 10.1210/jc.2009-2408. Epub 2010 Jun 23. J Clin Endocrinol Metab. 2010. PMID: 20573681

4

Metabolic disorders in newly diagnosed young adult female patients with simple virilizing 21-hydroxylase deficiency.

Zhang HJ, Yang J, Zhang MN, Liu CQ, Xu M, Li XJ, Yang SY, Li XY. Zhang HJ, et al. Among authors: zhang mn. Endocrine. 2010 Oct;38(2):260-5. doi: 10.1007/s12020-010-9382-9. Epub 2010 Oct 27. Endocrine. 2010. PMID: 20978868

5

A novel SRD5A2 mutation with loss of function identified in Chinese patients with hypospadias.

Zhang M, Yang J, Zhang H, Ning G, Li X, Sun S. Zhang M, et al. Horm Res Paediatr. 2011;76(1):44-9. doi: 10.1159/000324692. Epub 2011 May 3. Horm Res Paediatr. 2011. PMID: 21540559

6

[Clinical and genetic analysis of 11β-hydroxylase deficiency].

Sun SY, Zhang MN, Yang J, Zhang HJ, Liu JM, Hong J, Ning G, Li XY. Sun SY, et al. Among authors: zhang hj, zhang mn. Zhonghua Yi Xue Za Zhi. 2011 Nov 15;91(42):2999-3002. Zhonghua Yi Xue Za Zhi. 2011. PMID: 22333028 Chinese.

7

A prevalent and three novel mutations in CYP11B1 gene identified in Chinese patients with 11-beta hydroxylase deficiency.

Zhang M, Liu Y, Sun S, Zhang H, Wang W, Ning G, Li X. Zhang M, et al. J Steroid Biochem Mol Biol. 2013 Jan;133:25-9. doi: 10.1016/j.jsbmb.2012.08.011. Epub 2012 Sep 3. J Steroid Biochem Mol Biol. 2013. PMID: 22964742

8

New, recurrent, and prevalent mutations: Clinical and molecular characterization of 26 Chinese patients with 17alpha-hydroxylase/17,20-lyase deficiency.

Zhang M, Sun S, Liu Y, Zhang H, Jiao Y, Wang W, Li X. Zhang M, et al. J Steroid Biochem Mol Biol. 2015 Jun;150:11-6. doi: 10.1016/j.jsbmb.2015.02.007. Epub 2015 Feb 16. J Steroid Biochem Mol Biol. 2015. PMID: 25697092

9

Sequential Versus Continual Purified Urinary FSH/hCG in Men With Idiopathic Hypogonadotropic Hypogonadism.

Zhang M, Tong G, Liu Y, Mu Y, Weng J, Xue Y, Luo Z, Xue Y, Shi L, Wu X, Sun S, Zhu Y, Cao Y, Zhang J, Huang H, Niu B, Li H, Guo Q, Gao Y, Li Z, Ning G, Zhu D, Li X; HHIS Study Group. Zhang M, et al. J Clin Endocrinol Metab. 2015 Jun;100(6):2449-55. doi: 10.1210/jc.2014-3802. Epub 2015 Mar 31. J Clin Endocrinol Metab. 2015. PMID: 25825944 Clinical Trial.

10

The effectiveness of zinc supplementation in men with isolated hypogonadotropic hypogonadism.

Liu YL, Zhang MN, Tong GY, Sun SY, Zhu YH, Cao Y, Zhang J, Huang H, Niu B, Li H, Guo QH, Gao Y, Zhu DL, Li XY; Hypogonadotropic Hypogonadism Intervention Study (HHIS) Group. Liu YL, et al. Among authors: zhang j, zhang mn. Asian J Androl. 2017 May-Jun;19(3):280-285. doi: 10.4103/1008-682X.189621. Asian J Androl. 2017. PMID: 27768007 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

177 results

Search Page

Filters