Jiang L - Search Results

1

Mutation analysis of SCNN1B in a family with Liddle's syndrome.

Wang W, Zhou W, Jiang L, Cui B, Ye L, Su T, Wang J, Li X, Ning G. Wang W, et al. Among authors: jiang l. Endocrine. 2006 Jun;29(3):385-90. doi: 10.1385/ENDO:29:3:385. Endocrine. 2006. PMID: 16943574

2

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: jiang l. 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

3

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: jiang l. 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

4

[Leprechaunism: an inherited insulin resistance syndrome caused by the defect of insulin receptor].

Jiang L, Liu C, Wang WQ, Ye L, Zhu N, Zhou WW, Su TW, Li XY, Ning G. Jiang L, et al. Zhonghua Nei Ke Za Zhi. 2006 Sep;45(9):730-3. Zhonghua Nei Ke Za Zhi. 2006. PMID: 17166446 Chinese.

5

LOH on chromosome 11q, but not SDHD and Men1 mutations was frequently detectable in Chinese patients with pheochromocytoma and paraganglioma.

Sun HY, Cui B, Su DW, Jin XL, Sun FK, Zu Y, Jiang L, Wang WQ, Ning G. Sun HY, et al. Among authors: jiang l. Endocrine. 2006 Dec;30(3):307-12. doi: 10.1007/s12020-006-0009-0. Endocrine. 2006. PMID: 17526943

6

Overexpression of ERBB-2 was more frequently detected in malignant than benign pheochromocytomas by multiplex ligation-dependent probe amplification and immunohistochemistry.

Yuan W, Wang W, Cui B, Su T, Ge Y, Jiang L, Zhou W, Ning G. Yuan W, et al. Among authors: jiang l. Endocr Relat Cancer. 2008 Mar;15(1):343-50. doi: 10.1677/ERC-07-0188. Endocr Relat Cancer. 2008. PMID: 18310300 Free PMC article.

7

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: jiang l. Chin Med J (Engl). 2008 Apr 5;121(7):667-70. Chin Med J (Engl). 2008. PMID: 18466691 No abstract available.

8

Gene expression profiles of thymic neuroendocrine tumors (carcinoids) with ectopic ACTH syndrome reveal novel molecular mechanism.

Bi YF, Liu RX, Ye L, Fang H, Li XY, Wang WQ, Zhang J, Wang KK, Jiang L, Su TW, Chen ZY, Ning G. Bi YF, et al. Among authors: jiang l. Endocr Relat Cancer. 2009 Dec;16(4):1273-82. doi: 10.1677/ERC-08-0325. Epub 2009 Jul 22. Endocr Relat Cancer. 2009. PMID: 19625467

9

Diagnostic value of ACTH stimulation test in determining the subtypes of primary aldosteronism.

Jiang Y, Zhang C, Wang W, Su T, Zhou W, Jiang L, Zhu W, Xie J, Ning G. Jiang Y, et al. Among authors: jiang l. J Clin Endocrinol Metab. 2015 May;100(5):1837-44. doi: 10.1210/jc.2014-3551. Epub 2015 Feb 19. J Clin Endocrinol Metab. 2015. PMID: 25695882

10

Relationship between pituitary stalk (PS) visibility and the severity of hormone deficiencies: PS interruption syndrome revisited.

Wang W, Wang S, Jiang Y, Yan F, Su T, Zhou W, Jiang L, Zhang Y, Ning G. Wang W, et al. Among authors: jiang l, jiang y. Clin Endocrinol (Oxf). 2015 Sep;83(3):369-76. doi: 10.1111/cen.12788. Epub 2015 May 7. Clin Endocrinol (Oxf). 2015. PMID: 25845766

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