Zhao X - Search Results

1

Clinical Relevance of Gain- and Loss-of-Function Germline Mutations in STAT1: A Systematic Review.

Zhang W, Chen X, Gao G, Xing S, Zhou L, Tang X, Zhao X, An Y. Zhang W, et al. Among authors: zhao x. Front Immunol. 2021 Mar 11;12:654406. doi: 10.3389/fimmu.2021.654406. eCollection 2021. Front Immunol. 2021. PMID: 33777053 Free PMC article.

2

[Clinical analysis of 942 cases of Kawasaki disease].

Zhang W, Li Q, Zhao XD, Tang XM, Wang XG, Wang M, Wu DQ, Ou Q, Yang XQ. Zhang W, et al. Zhonghua Er Ke Za Zhi. 2006 May;44(5):324-8. Zhonghua Er Ke Za Zhi. 2006. PMID: 16780705 Chinese.

3

[A compound heterozygosity mutation in the interleukin-7 receptor-alpha gene resulted in severe combined immunodeficiency in a Chinese patient].

Zhang ZY, Zhao XD, Wang M, Yu J, An YF, Yang XQ. Zhang ZY, et al. Zhonghua Er Ke Za Zhi. 2009 Sep;47(9):691-5. Zhonghua Er Ke Za Zhi. 2009. PMID: 20021794 Chinese.

4

[A novel missense mutation of FOXP3 causes immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in a Chinese child].

An YF, Zhao XD, Xu F, Yang XQ. An YF, et al. Zhonghua Er Ke Za Zhi. 2009 Nov;47(11):824-8. Zhonghua Er Ke Za Zhi. 2009. PMID: 20078992 Chinese.

5

Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome.

Zhang ZY, Zhao XD, Jiang LP, Liu EM, Cui YX, Wang M, Wei H, Yu J, An YF, Yang XQ. Zhang ZY, et al. Pediatr Allergy Immunol. 2011 Aug;22(5):482-7. doi: 10.1111/j.1399-3038.2010.01126.x. Epub 2011 Mar 29. Pediatr Allergy Immunol. 2011. PMID: 21771083

6

[Genetic and proteinic analysis of a Chinese boy with X-linked lymphoproliferative disease and his maternal relatives].

Yang X, Wang J, An YF, Kanegane H, Miyawaki T, Zhao XD. Yang X, et al. Among authors: zhao xd. Zhonghua Er Ke Za Zhi. 2011 Jun;49(6):416-20. Zhonghua Er Ke Za Zhi. 2011. PMID: 21924052 Chinese.

7

[Pay attention to the progress in pediatric rheumatic diseases in China].

Tang XM, Zhao XD, Yang XQ. Tang XM, et al. Zhonghua Er Ke Za Zhi. 2011 Jul;49(7):481-4. Zhonghua Er Ke Za Zhi. 2011. PMID: 22088174 Chinese. No abstract available.

8

Clinical characteristics and mutation analysis of X-linked severe combined immunodeficiency in China.

Zhang C, Zhang ZY, Wu JF, Tang XM, Yang XQ, Jiang LP, Zhao XD. Zhang C, et al. World J Pediatr. 2013 Feb;9(1):42-7. doi: 10.1007/s12519-011-0330-4. Epub 2011 Nov 21. World J Pediatr. 2013. PMID: 22105576

9

[Screening for cytotoxic defects with flow cytometric detection of CD107α on natural killer cells and cytotoxic lymphocyte cells].

Wang J, Liu Z, Jiang LP, An YF, Zhao XD. Wang J, et al. Zhonghua Er Ke Za Zhi. 2012 May;50(5):386-91. Zhonghua Er Ke Za Zhi. 2012. PMID: 22883044 Chinese.

10

Clinical features and mutation analysis of X-linked agammaglobulinemia in 20 Chinese patients.

Qin X, Jiang LP, Tang XM, Wang M, Liu EM, Zhao XD. Qin X, et al. Among authors: zhao xd. World J Pediatr. 2013 Aug;9(3):273-7. doi: 10.1007/s12519-013-0400-x. Epub 2013 Jan 18. World J Pediatr. 2013. PMID: 23335184

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