Liu XQ - Search Results

1

[Role of caspase-3, -8, and -9 in apoptosis of copper induced primary cortical neurons].

Jiao XT, Liu XQ, Huang LS, Zhang YJ, Han LS. Jiao XT, et al. Among authors: liu xq. Zhongguo Dang Dai Er Ke Za Zhi. 2009 Nov;11(11):917-22. Zhongguo Dang Dai Er Ke Za Zhi. 2009. PMID: 20113661 Free article. Chinese.

2

[Prenatal diagnosis of glycogen storage disease Ia by screening for hot spot mutations in combination with the 1176 nucleotide polymorphism linkage analysis].

Qiu WJ, Zhang YF, Pan J, Ye J, Liu XQ, Han LS, Gu XF. Qiu WJ, et al. Among authors: liu xq. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Feb;22(1):44-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15696478 Chinese.

3

[Screening for tetrahydrobiopterin metabolic disorders and related gene analysis among the patients with motor disturbance and mental retardation].

Ye J, Liu XQ, Qiu WJ, Han LS, Zhou JD, Zhang YF, Gu XF. Ye J, et al. Among authors: liu xq. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Apr;24(2):210-2. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 17407085 Chinese.

4

[Genetic tests and clinical re-evaluation of 85 children with suspected spinal muscular atrophy].

Ji X, Liu XQ, Shen JW, Li XH, Tao J. Ji X, et al. Among authors: liu xq. Zhonghua Er Ke Za Zhi. 2010 Jun;48(6):425-30. Zhonghua Er Ke Za Zhi. 2010. PMID: 21055263 Chinese.

5

[Diagnostic value of neuronal nitric oxide synthase antibody for clinically suspected Becker muscular dystrophy].

Li XH, Zhao L, Wu Y, Wu J, He DK, Liu XQ. Li XH, et al. Among authors: liu xq. Zhongguo Dang Dai Er Ke Za Zhi. 2011 Apr;13(4):288-91. Zhongguo Dang Dai Er Ke Za Zhi. 2011. PMID: 21507296 Free article. Chinese.

6

Metal element excretion in 24-h urine in patients with Wilson disease under treatment of D-penicillamine.

Huang L, Yu X, Zhang J, Liu X, Zhang Y, Jiao X, Yu X. Huang L, et al. Biol Trace Elem Res. 2012 May;146(2):154-9. doi: 10.1007/s12011-011-9250-3. Epub 2011 Nov 11. Biol Trace Elem Res. 2012. PMID: 22076732

7

[The value of high-frequency ultrasound in the diagnosis of duchenne muscular dystrophy in children].

Shi YR, Liu XQ, Dai H, Lu DY, Ni JY, Li XH. Shi YR, et al. Among authors: liu xq. Zhongguo Dang Dai Er Ke Za Zhi. 2012 Jul;14(7):533-5. Zhongguo Dang Dai Er Ke Za Zhi. 2012. PMID: 22809609 Free article. Chinese.

8

[Genotype and phenotype correlation in Chinese patients with Wilson's Disease].

Liu XQ, Zhang YF, Liu TT, Gu XF, Hsiao KJ, Bao KR, Yu LH. Liu XQ, et al. Among authors: liu tt. Zhonghua Er Ke Za Zhi. 2003 Jan;41(1):35-8. Zhonghua Er Ke Za Zhi. 2003. PMID: 14761325 Chinese.

9

[Clinical and genetic analysis of two unrelated patients with Angelman syndrome and novel UBE3A mutations].

Xu H, Ji X, Xu Y, Liu X, Zhang J, Chen Y, Xiao B. Xu H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):826-830. doi: 10.3760/cma.j.issn.1003-9406.2017.06.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188609 Chinese.

10

[Clinical application of multiplex ligation-dependent probe amplification for the detection exonic copy number alterations in the Dystrophin gene].

Long F, Sun W, Ji X, Li XH, Liu XQ, Jiang WT, Tao J. Long F, et al. Among authors: liu xq. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Dec;28(6):699-704. doi: 10.3760/cma.j.issn.1003-9406.2011.06.023. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 22161109 Chinese.

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