Xiong H - Search Results

1

Survival analysis of a cohort of Chinese patients with mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) based on clinical features.

Zhang Z, Zhao D, Zhang X, Xiong H, Bao X, Yuan Y, Wang Z. Zhang Z, et al. Among authors: xiong h. J Neurol Sci. 2018 Feb 15;385:151-155. doi: 10.1016/j.jns.2017.12.033. Epub 2017 Dec 29. J Neurol Sci. 2018. PMID: 29406897

2

[Diagnosis and treatment of biotinidase deficiency-clinical study of six patients].

Yang YL, Yamaguchi S, Tagami Y, Zhang YH, Xiong H, Hasegawa Y, Kimura M, Hanai J, Fujita K, Qian N, He XJ, Wu Y, Bao XH, Qin J, Wu X. Yang YL, et al. Among authors: xiong h. Zhonghua Er Ke Za Zhi. 2003 Apr;41(4):249-51. Zhonghua Er Ke Za Zhi. 2003. PMID: 14754524 Chinese.

3

[X-linked adrenoleukodystrophy ABCD1 gene mutation analysis in China].

Pan H, Xiong H, Zhang YH, Wu Y, Bao XH, Jiang YW, Wu XR. Pan H, et al. Among authors: xiong h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Feb;21(1):1-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 14767898 Chinese.

4

[Screening for carrier and prenatal diagnosis of X-linked adrenoleukodystrophy].

Wang AH, Bao XH, Xiong H, Pan H, Wu Y, Zhang YH, Shi CY, Qin J, Wu XR. Wang AH, et al. Among authors: xiong h. Zhonghua Er Ke Za Zhi. 2005 May;43(5):345-9. Zhonghua Er Ke Za Zhi. 2005. PMID: 15924749 Chinese.

5

ABCD1 gene mutations in Chinese patients with X-linked adrenoleukodystrophy.

Pan H, Xiong H, Wu Y, Zhang YH, Bao XH, Jiang YW, Wu XR. Pan H, et al. Among authors: xiong h. Pediatr Neurol. 2005 Aug;33(2):114-20. doi: 10.1016/j.pediatrneurol.2005.03.006. Pediatr Neurol. 2005. PMID: 16087056

6

[Research progress on congenital muscular dystrophy].

Xiong H, Yuan Y, Wu XR. Xiong H, et al. Zhonghua Er Ke Za Zhi. 2005 Dec;43(12):958-61. Zhonghua Er Ke Za Zhi. 2005. PMID: 16412372 Review. Chinese. No abstract available.

7

The genotype and phenotype studies of 40 Chinese patients with X-linked adrenoleukodystrophy (X-ALD).

Ping LL, Bao XH, Wang AH, Pan H, Wu Y, Xiong H, Zhang YH, Jiang YW, Qin J, Wu XR. Ping LL, et al. Among authors: xiong h. Beijing Da Xue Xue Bao Yi Xue Ban. 2006 Feb 18;38(1):66-70. Beijing Da Xue Xue Bao Yi Xue Ban. 2006. PMID: 16415970 Free article.

8

[Diagnostic value of muscle, sural nerve and skin biopsies in childhood neuromuscular disorders].

Chang XZ, Zhou JY, Yuan Y, Wu Y, Li YX, Zhang W, Jiang YW, Bao XH, Zhang YH, Wang S, Xiong H, Yang YL, Qin J. Chang XZ, et al. Among authors: xiong h. Zhonghua Er Ke Za Zhi. 2006 Dec;44(12):909-12. Zhonghua Er Ke Za Zhi. 2006. PMID: 17254458 Chinese.

9

[Diagnosis of congenital muscular dystrophy and clinical significance of merosin expression].

Xiong H, Yao S, Yuan Y, Chang XZ, Wu Y, Bao XH, Zhang YH, Wu HS, Chen L, Qin J, Wu XR. Xiong H, et al. Zhonghua Er Ke Za Zhi. 2006 Dec;44(12):918-23. Zhonghua Er Ke Za Zhi. 2006. PMID: 17254461 Chinese.

10

Screening of common mitochondrial mutations in Chinese patients with mitochondrial encephalomyopathies.

Qi Y, Zhang Y, Wang Z, Yang Y, Yuan Y, Niu S, Pei P, Wang S, Ma Y, Bu D, Zou L, Fang F, Xiao J, Sun F, Zhang Y, Wu Y, Wang S, Xiong H, Wu X. Qi Y, et al. Among authors: xiong h. Mitochondrion. 2007 Feb-Apr;7(1-2):147-50. doi: 10.1016/j.mito.2006.11.019. Epub 2006 Dec 9. Mitochondrion. 2007. PMID: 17276742

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