Xiao JX - Search Results

1

Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome.

Yang YL, Sun F, Zhang Y, Qian N, Yuan Y, Wang ZX, Qi Y, Xiao JX, Wang XY, Qi ZY, Zhang YH, Jiang YW, Bao XH, Qin J, Wu XR. Yang YL, et al. Among authors: xiao jx. Chin Med J (Engl). 2006 Mar 5;119(5):373-7. Chin Med J (Engl). 2006. PMID: 16542579

2

[Clinical characteristics of X-linked adrenoleukodystrophy].

Xiong H, Zhang YH, Qin J, Xiao JX, Shi CY, Zhou SM, Wu XR. Xiong H, et al. Among authors: xiao jx. Zhonghua Er Ke Za Zhi. 2003 Mar;41(3):203-7. Zhonghua Er Ke Za Zhi. 2003. PMID: 14756960 Chinese.

3

Quantification of cerebral blood flow by flow-sensitive alternating inversion recovery exempting separate T1 measurement in healthy volunteers.

Xiao JX, Zhang XH, Xie S, Zou RL. Xiao JX, et al. Chin Med J (Engl). 2006 Dec 20;119(24):2096-100. Chin Med J (Engl). 2006. PMID: 17240566

4

[Clinical characteristics of cases with leukoencephalopathy with vanishing white matter].

Wu Y, Jiang YW, Qin J, Xiao JX, Wang JM, Yang YL, Zhang YH, Chang XZ, Lin Q, Wu XR. Wu Y, et al. Among authors: xiao jx. Zhonghua Er Ke Za Zhi. 2007 Feb;45(2):115-20. Zhonghua Er Ke Za Zhi. 2007. PMID: 17456339 Chinese.

5

[Leigh syndrome due to pyruvate dehydrogenase E1 alpha subunit gene mutation: a complicated and difficult case study].

Zhang Y, Sun F, Yang YL, Chang XZ, Qi Y, Qi ZY, Xiao JX, Qin J, Wu XR. Zhang Y, et al. Among authors: xiao jx. Zhongguo Dang Dai Er Ke Za Zhi. 2007 Jun;9(3):216-9. Zhongguo Dang Dai Er Ke Za Zhi. 2007. PMID: 17582259 Chinese.

6

Spinal cord demyelination associated with biotinidase deficiency in 3 Chinese patients.

Yang Y, Li C, Qi Z, Xiao J, Zhang Y, Yamaguchi S, Hasegawa Y, Tagami Y, Jiang Y, Xiong H, Zhang Y, Qin J, Wu XR. Yang Y, et al. J Child Neurol. 2007 Feb;22(2):156-60. doi: 10.1177/0883073807300307. J Child Neurol. 2007. PMID: 17621476

7

Heterogeneity of magnetic resonance imaging in Leigh syndrome with SURF1 gene 604G-->C mutation.

Xie S, Xiao JX, Qi ZY, Yang YL, Jiang XX. Xie S, et al. Among authors: xiao jx. Clin Imaging. 2009 Jan-Feb;33(1):1-6. doi: 10.1016/j.clinimag.2008.08.001. Clin Imaging. 2009. PMID: 19135921

8

[A case of Leigh syndrome associated with respiratory chain complex I deficiency due to mitochondrial gene 13513G>A mutation].

Wei XQ, Kong QP, Zhang Y, Yang YL, Chang XZ, Qi Y, Qi ZY, Xiao JX, Qin J, Wu XR. Wei XQ, et al. Among authors: xiao jx. Zhongguo Dang Dai Er Ke Za Zhi. 2009 May;11(5):333-6. Zhongguo Dang Dai Er Ke Za Zhi. 2009. PMID: 19470250 Chinese.

9

The appearance of ADCs in the non-affected areas of the patients with MELAS.

Liu Z, Liu X, Hui L, Zhao D, Wang X, Xie S, Xiao J, Jiang X. Liu Z, et al. Neuroradiology. 2011 Apr;53(4):227-32. doi: 10.1007/s00234-010-0729-y. Epub 2010 Jun 17. Neuroradiology. 2011. PMID: 20556599

10

[Leucodystrophy induced by late onset 3-hydroxy-3-methylglutaric aciduria].

Ma YY, Song JQ, Wu TF, Liu YP, Xiao JX, Jiang YW, Yang YL. Ma YY, et al. Among authors: xiao jx. Zhongguo Dang Dai Er Ke Za Zhi. 2011 May;13(5):392-5. Zhongguo Dang Dai Er Ke Za Zhi. 2011. PMID: 21575345 Free article. Chinese.

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