Chang GY - Search Results

1

[Analysis of clinical manifestations and genetic mutations in a child with Laron syndrome].

Chang GY, Chen SK, Gu XF, Gong ZW, Zhang QG. Chang GY, et al. Zhonghua Er Ke Za Zhi. 2013 Dec;51(12):930-3. Zhonghua Er Ke Za Zhi. 2013. PMID: 24495765 Chinese.

2

[Long-term follow-up of isolated-growth hormone deficiency typeIA: the clinical analysis of 2-sister cases].

Chang GY, Dong ZY, Wang W, Wang DF. Chang GY, et al. Zhonghua Er Ke Za Zhi. 2010 Dec;48(12):944-6. Zhonghua Er Ke Za Zhi. 2010. PMID: 21215191 Chinese.

3

[Association of 45, X/46, XY mosaicism with disorders of sex development: the clinical analysis of 5 cases].

Chang GY, Dong ZY, Wang W, Xiao Y, Chen FS, Ni JH, Wang RF, Wang DF. Chang GY, et al. Zhonghua Er Ke Za Zhi. 2011 Jun;49(6):451-4. Zhonghua Er Ke Za Zhi. 2011. PMID: 21924060 Chinese.

4

SIDT2 is involved in the NAADP-mediated release of calcium from insulin secretory granules.

Chang G, Yang R, Cao Y, Nie A, Gu X, Zhang H. Chang G, et al. J Mol Endocrinol. 2016 Apr;56(3):249-59. doi: 10.1530/JME-15-0227. Epub 2016 Jan 7. J Mol Endocrinol. 2016. PMID: 26744456

5

[Endocrine and metabolic features of female children with Prader-Willi syndrome: an analysis of 4 cases].

Wu ML, Li J, Ding Y, Chen Y, Chang GY, Wang XM, Wang J, Shen YP. Wu ML, et al. Among authors: chang gy. Zhongguo Dang Dai Er Ke Za Zhi. 2017 May;19(5):514-518. doi: 10.7499/j.issn.1008-8830.2017.05.007. Zhongguo Dang Dai Er Ke Za Zhi. 2017. PMID: 28506340 Free PMC article. Chinese.

6

[Analysis of clinical manifestation and genetic mutation in a child with X-linked chondrodysplasia punctata 2].

Chang G, Zhou Y, Yin L, Gu L, Ying D, Chen H, Wang X, Wang J. Chang G, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Aug 10;35(4):527-530. doi: 10.3760/cma.j.issn.1003-9406.2018.04.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30098249 Chinese.

7

[Clinical and genetic analysis of an infant with combined pituitary hormone deficiency due to POU1F1 gene variants].

Li Q, Li J, Chang G, Ding Y, Wang Y, Shen Y, Wang J, Wang X. Li Q, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Sep 10;37(9):1018-1020. doi: 10.3760/cma.j.cn511374-20190921-00486. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32820520 Chinese.

8

Evaluating the variety of GNAS inactivation disorders and their clinical manifestations in 11 Chinese children.

Chang G, Li Q, Li N, Li G, Li J, Ding Y, Huang X, Shen Y, Wang J, Wang X. Chang G, et al. BMC Endocr Disord. 2022 Mar 16;22(1):70. doi: 10.1186/s12902-022-00941-8. BMC Endocr Disord. 2022. PMID: 35296306 Free PMC article.

9

[Clinical characteristics and genetic analysis of a patient with STISS syndrome due to variant of PSMD12 gene].

Xu L, Wang Y, Zhang Q, Chen Y, Chang G, Wang X, Wang J, Ding Y. Xu L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Mar 10;40(3):349-353. doi: 10.3760/cma.j.cn511374-20220207-00097. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 36854413 Review. Chinese.

10

[Identification of a child with Teebi hypertelorism syndrome 1 due to variant of SPECC1L gene].

Li Z, Wang Y, Li X, Feng B, Gu S, Yang F, Chang G, Wang J, Wang X. Li Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Aug 10;40(8):998-1003. doi: 10.3760/cma.j.cn511374-20220823-00574. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 37532501 Chinese.

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