Wang X - Search Results

1

Analysis of TAP1 and TAP2 polymorphism of mother-infant in Chinese patients with pre-eclampsia.

Zhang Z, Jia L, Hou L, Xiong P, Wu X, Wang X, Huang Y, Ke H, Chang C, Cui S, Gong F. Zhang Z, et al. Among authors: wang x. Cell Mol Immunol. 2005 Apr;2(2):141-4. Cell Mol Immunol. 2005. PMID: 16191421 Free article.

2

Impact of gonadotropins on oocyte maturation, fertilisation and developmental competence in vitro.

Wang X, Tsai T, Qiao J, Zhang Z, Feng HL. Wang X, et al. Reprod Fertil Dev. 2014 Jun;26(5):752-7. doi: 10.1071/RD13024. Reprod Fertil Dev. 2014. PMID: 23726536

3

[Bodily symptoms associated with mental disorders in two children].

Lu S, Liu LJ, Sui J, Wang XM. Lu S, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2010 Sep;12(9):756-7. Zhongguo Dang Dai Er Ke Za Zhi. 2010. PMID: 20849732 Free article. Chinese. No abstract available.

4

[Related factors of insulin sensitivity in infants].

Fu TR, Wang XL, Tong XM, Wang XM. Fu TR, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2010 Mar;12(3):238-41. Zhongguo Dang Dai Er Ke Za Zhi. 2010. PMID: 20350443 Free article. Review. Chinese. No abstract available.

5

[Histiocytic necrotic lymphadenitis as an initial presentation in two children with Sjogren's syndrome and/or systemic lupus erthematous].

Lu S, Zhang J, Zhou W, Wang XM. Lu S, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2010 Apr;12(4):311-2. Zhongguo Dang Dai Er Ke Za Zhi. 2010. PMID: 20416233 Chinese. No abstract available.

6

[A case report of incessant atrial tachycardia complicated by tachyarrhythmic cardiomyopathy].

Lu S, Chen XF, Wang XM. Lu S, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2011 Aug;13(8):688-9. Zhongguo Dang Dai Er Ke Za Zhi. 2011. PMID: 21849127 Free article. Chinese. No abstract available.

7

[A survey of pubertal development in children born with assisted reproductive technology].

Liu ZY, Wang XL, Han TY, Cui YP, Wang XM, Tong XM, Song Y, Wang HJ, Li S. Liu ZY, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2017 Jun;19(6):646-651. doi: 10.7499/j.issn.1008-8830.2017.06.007. Zhongguo Dang Dai Er Ke Za Zhi. 2017. PMID: 28606230 Free PMC article. Chinese.

8

WITHDRAWN: Two Novel Heterozygous Mutations of CSA Cause Cockayne Syndrome in a Chinese Family.

Cui YP, Chen YY, Wang XM, Wang XL, Nan X, Zhao H. Cui YP, et al. Among authors: wang xl, wang xm. Pediatr Neurol. 2014 Mar 22:S0887-8994(14)00160-X. doi: 10.1016/j.pediatrneurol.2014.03.009. Online ahead of print. Pediatr Neurol. 2014. PMID: 25824604

9

Two Novel Heterozygous Mutations in ERCC8 Cause Cockayne Syndrome in a Chinese Patient.

Cui YP, Chen YY, Wang XM, Wang XL, Nan X, Zhao H. Cui YP, et al. Among authors: wang xl, wang xm. Pediatr Neurol. 2015 Sep;53(3):262-5. doi: 10.1016/j.pediatrneurol.2015.06.006. Epub 2015 Jun 14. Pediatr Neurol. 2015. PMID: 26173784

10

Case Report: Improved Height in a Patient With Myhre Syndrome Using a Combination of Growth Hormone and Letrozole.

Wu H, Wang X, Cui Y, Wang X. Wu H, et al. Among authors: wang x. Front Pediatr. 2021 Jul 29;9:675934. doi: 10.3389/fped.2021.675934. eCollection 2021. Front Pediatr. 2021. PMID: 34395338 Free PMC article.

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