Ning G - Search Results

1

Characteristics of ectopic adrenocorticotropic hormone syndrome due to thymic carcinoid and analysis of the molecular mechanism.

Bi YF, Ye L, Chen YH, Ning G, Sun SY, Jiang L, Zhu N, Zhou WW, Wang WQ. Bi YF, et al. Among authors: ning g. Chin Med J (Engl). 2008 Apr 5;121(7):667-70. Chin Med J (Engl). 2008. PMID: 18466691 No abstract available.

2

[Fasting serum free fatty acid, insulin sensitivity index and serum lipid levels in individuals with different body mass index and glucose tolerance].

Zhang YF, Hong J, Gu WQ, Sun SY, Tang JF, Jiang L, Dai M, Zhao YJ, Ning G. Zhang YF, et al. Among authors: ning g. Zhonghua Nei Ke Za Zhi. 2003 Nov;42(11):793-6. Zhonghua Nei Ke Za Zhi. 2003. PMID: 14636469 Chinese.

3

Multiple endocrine neoplasia type 2B caused by a single point mutation in RET proto-oncogene in a Chinese patient.

Zhang YF, Hong J, Zhao YJ, Jiang L, Dai M, Jin XL, Chen JL, Ning G. Zhang YF, et al. Among authors: ning g. Chin Med J (Engl). 2004 Aug;117(8):1262-4. Chin Med J (Engl). 2004. PMID: 15361307 No abstract available.

4

Relationships between the changes of serum levels of OPG and RANKL with age, menopause, bone biochemical markers and bone mineral density in Chinese women aged 20-75.

Liu JM, Zhao HY, Ning G, Zhao YJ, Chen Y, Zhang Zh, Sun LH, Xu MY, Chen JL. Liu JM, et al. Among authors: ning g. Calcif Tissue Int. 2005 Jan;76(1):1-6. doi: 10.1007/s00223-004-0007-2. Epub 2004 Oct 7. Calcif Tissue Int. 2005. PMID: 15455183

5

Autosomal dominant neurohypophyseal diabetes insipidus with linkage to chromosome 20p13 but without mutations in the AVP-NPII gene.

Ye L, Li X, Chen Y, Sun H, Wang W, Su T, Jiang L, Cui B, Ning G. Ye L, et al. Among authors: ning g. J Clin Endocrinol Metab. 2005 Jul;90(7):4388-93. doi: 10.1210/jc.2004-2000. Epub 2005 Apr 5. J Clin Endocrinol Metab. 2005. PMID: 15811933

6

Hypomethylation in the promoter region of POMC gene correlates with ectopic overexpression in thymic carcinoids.

Ye L, Li X, Kong X, Wang W, Bi Y, Hu L, Cui B, Li X, Ning G. Ye L, et al. Among authors: ning g. J Endocrinol. 2005 May;185(2):337-43. doi: 10.1677/joe.1.05963. J Endocrinol. 2005. PMID: 15845926

7

[Changes of growth hormone and insulin-like growth factor axis in patients with anorexia nervosa and its clinical significance].

Lu JL, Zhao YJ, Liu JM, Tang JF, Jiang XH, Hong J, Wang S, Wang WQ, Ning G. Lu JL, et al. Among authors: ning g. Zhonghua Yi Xue Za Zhi. 2005 Jan 19;85(3):203-4. Zhonghua Yi Xue Za Zhi. 2005. PMID: 15854469 Chinese. No abstract available.

8

[SRY negative 46XX male syndrome--a case report].

Sun SY, Zhang W, Liu JM, Zhao YJ, Ning G, Li XY. Sun SY, et al. Among authors: ning g. Zhonghua Yi Xue Za Zhi. 2005 Feb 2;85(5):358-9. Zhonghua Yi Xue Za Zhi. 2005. PMID: 15854519 Chinese. No abstract available.

9

[Hereditary spinocerebellar ataxia--a family pedigree with SCA3 gene mutation].

Jiang XH, Ye L, Fu Y, Yu HZ, Yu GP, Zhao YJ, Ning G, Li XY. Jiang XH, et al. Among authors: ning g. Zhonghua Yi Xue Za Zhi. 2005 Mar 30;85(12):848-9. Zhonghua Yi Xue Za Zhi. 2005. PMID: 15949406 Chinese. No abstract available.

10

Mutation screening in Chinese hypokalemic periodic paralysis patients.

Wang W, Jiang L, Ye L, Zhu N, Su T, Guan L, Li X, Ning G. Wang W, et al. Among authors: ning g. Mol Genet Metab. 2006 Apr;87(4):359-63. doi: 10.1016/j.ymgme.2005.10.020. Epub 2006 Jan 4. Mol Genet Metab. 2006. PMID: 16386935

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